CJC 1295/Ipamorelin is a combination of 2 peptides. It is a Growth Hormone releasing hormone that stimulates one side of the pituitary gland. It does this in order to produce growth hormone. Ipamorelin mimics the ghrelin and binds to the ghrelin receptor in the pituitary gland in the brain. Thus, it also acts on the pituitary gland in order to produce growth hormone. These two peptides combine to act together in order to increase HGH (human growth hormone) produced in the body. The CJC 1295/Ipamorelin combo is able to achieve this by acting in two different families of receptors. 
What is CJC 1295?
A synthetically produced peptide, CJC 1295 was originally made to treat diseases, but has been discovered to have performance-enhancing effects that appeal to athletes. The peptide works by increasing protein synthesis and insulin-like growth factor levels. This process enables muscle tissue to grow, thereby increasing muscle mass and function.
What Is Ipamorelin?
is a hormone secretagogue, meaning it helps excrete hormones into the bloodstream while simulating the pituitary gland to produce them. It serves other functions as well. Ipamorelin is associated with improved cognitive skills, memory, pain relief, and internal body temperature regulation along with growth and muscle development. 
How does CJC 1295 work?
Ipamorelin and CJC 1295 are often used together to stimulate muscle development. The combination works by increasing the blood level of hormones associated with growth. It can increase muscle mass and strength, decrease body fat, improve injury recovery time, and even improve sleep quality and cognitive function.
Research completed with healthy men and women between the ages of 21 and 61, showed that CJC-1295 had the ability to increase serum growth hormone levels by 200-1000%. In these individuals, the elevated growth hormone production and release continued for up to 6 days because CJC-1295 has a half life of about 6-8 days. This longer half-life means the body continues to produce beyond the day of injection and is thought to be a great benefit has compared to other peptides that also have similar actions. For this reason and a few more, CJC-1295 has become very effective peptide for safely increasing growth hormone levels. 
What are the benefits of CJC1295?
- Increased Bone Density: As we get older, our bones get brittle, that is why injuries are more common.
- Increase in muscle mass
- Strengthens the cardiovascular system: More muscle mass = higher metabolism = less body fat
- The ability to burn fat: With an increase in muscle mass allows the body’s resting metabolic rate is boosted leading to more calories burned throughout the day.
- Increased Sex drive: Sex his huge. Not being able to function properly sexually can really take a toll on your mental well-being.
- Improved Recovery and Repair from Injuries: Being on a proper bio-identical hormone replacement therapy program leads to an overall improved state of well-being. This adheres to recovery time (soreness) and acute musculoskeletal injuries.
- Strengthens Immune System: It is a tremendous benefit when you are trying to attain optimal health and that is achieved by having a strong immune system
Improves cognition and memory function-It is an improved overall benefit to the body, this includes focus and feeling mental clarity and sharpness throughout the day.
Improves Insulin Sensitivity-CJC 1295 and Ipamorelin improves insulin sensitivity thus reducing the body’s triglycerides. High blood sugars are reduced which helps burning more body fat.
Who is a good candidate for CJC 1295 / Ipamorelin?
CJC-1295 can help individuals over the age of 30 to have more energy, a faster metabolism, and stay in better shape as you age. It’s not a hormone itself, so it is a relatively safe and low-risk option when all things are considered. However, it requires a prescription and is delivered via an injection, so there are some important points to cover regarding the CJC-1295 benefits and side effects trade-offs.
What are the side effects of CJC1295 / Ipamorelin?
One of the biggest reasons why CJC-1295 is being embraced by so many in their anti-aging fight is because of the relatively low rate of side effects. Most people tolerate CJC-1295 quite well, and side effects are generally mild if present at all. The most frequent side effect was injection site reaction – usually skin complaints or mild pain at the site of injection.
Most common side effects are: Sensitivity, soreness, or pain at the injection site, Flu-like symptoms, Headache, Dizzines, Nausea, Drowsiness, Flushing, Hives or other skin reactions, Hyperactivity, Difficulty swallowing
Our Conclusion on CJC 1295 / Ipamorelin peptides:
The effects of CJC-1295 have been researched thoroughly. It is beneficial in building muscle, losing body fat, and boosting energy levels. It does all these by facilitating the production of more growth hormone for your body.
CJC-1295 is a releasing factor for growth hormone and is therefore considered a Prohibited Substance under Section S2 of the WADA Prohibited List. This substance has potential performance-enhancing effects, it is readily available, and there is reason to believe that it is being used within the bodybuilding community.
FREQUENTLY ASKED QUESTIONS ON CJC1295 / IPAMORELIN
Why combine CJC-1295 & IPAMORELIN?
CJC-1295 and Ipamorelin are typically combined in therapy because the are known to work well together. CJC-1295 takes anywhere from 1-4 hours to reach peak serum in the blood, while Ipamorelin works much quicker. Ipamorelin is cleared from the body more rapidly as it’s half life is about 2 hours. The combination of both peptides ensures a rapid onset with Ipamorelin and lasting effects with CJC-1295. These 2 peptides are incredibly specific at increasing growth hormone levels when compared to other peptides. Other peptide can increase levels of cortisol (as seen with stress, can increase hunger) but neither Ipamorelin nor CJC-1295 have an effect on other hormones which is a great advantage.
How often should you take CJC-1295?
Most prescribers direct that CJC-1295 be taken once daily, via subcutaneous injection (above the muscle, below the skin) in the stomach or abdominal region. Other prescribers recommend a “5 days a week” plan, either with skipping days every 2 or 3 days, or weekdays on, weekends off for injections. There is competing evidence as to the efficacy of these two dosing regimens, but in both cases, the effects of CJC-1295 – higher circulating levels of human growth hormone – tend to last for upwards of a week following administration and continue at that level so long as the administration continues a few times a week.
Does CJC 1295 really work?
The effects of CJC-1295 have been researched thoroughly. It is beneficial in building muscle, losing body fat, and boosting energy levels. It does all these by facilitating the production of more growth hormone for your body.
How long can you take CJC 1295?
Research has shown that administering CJC-1295 once weekly helps to increase plasma GH concentrations (2-10 times more) for a period of up to 6 days after injection. Further, it increases IGF-1 levels by 1.5 to 3 times, for a period of 9 to 11 days, with no adverse side effects.
How should CJC-1295/Ipamorelin be used?
CJC-1295/Ipamorelin is injected subcutaneously or under the skin. The injection is taken at night to mimic the natural release cycle of growth hormone.
BIOIDENTICAL HORMONE REPLACEMENT THERAPY
TESTOSTERONE REPLACEMENT THERAPY
HUMAN GROWTH HORMONE TREATMENT
Peptides are the newly emerging science of cell signaling amino acid sequences, with far-reaching regulatory and rejuvenation actions on neuro-endocrine-immune functionality. The specifically targeted use of peptides in the environment has the potential to rewrite bodily chemistry relationships, and ultimately generate a restorative trend towards anabolism and homeostasis. Peptides can also be utilized and applied in the treatment of injuries, with capabilities that help prevent aging, illness, and enhance peak performance.
Types of Peptides: Clickable link to information on each peptide. Information below
Sermorelin Therapy in Washington, DC
After Roger Guillemin and Andrew Schally were awarded the 1977 Nobel Prize in Medicine for their work on neuroendocrine releasing factors, the precise chemical structure of GHRH, a 44 amino acid peptide, was determined using tissue from human pancreatic tumors that caused acromegaly, a disease resulting from excess secretion of GH.1 The following year, Wehrenberg and Ling2 sought to determine which part of the molecule was essential for its pituitary stimulating action. By eliminating individual amino acids and then testing the remaining peptide fragments, they found that only the first 29 amino acids are needed for stimulating pituitary production and secretion of HGH. Consequently, this fragment of the native molecule, commonly known as Sermorelin is often used to treat GH deficient states in children and adults
Chemically, sermorelin is known as growth hormone releasing factor (GRF) or growth hormone releasing hormone (GRH)1-29 NH2 indicating that the amino terminus is at position 29. However, the molecule is not used clinically as the free base, but rather as the acetic acid salt, i.e. as sermorelin acetate. The free base of sermorelin has the empirical formula C149H246N44O42S and a molecular weight of 3,358 daltons3 Sermorelin acetate is a sterile, non-pyrogenic, lyophilized powder intended for subcutaneous injection after reconstitution with Bacteriostatic Water for Injection and should be stored at between 36 and 46° F (2 and 8° C). Taxonomically, sermorelin is listed as an organic compound (kingdom), an organic acid (superclass), a carboxylic acid (class), amino acid/peptide analogue (subclass), and as a peptide (direct parent).4
Growth Hormone Replacement
Growth hormone replacement therapy (GHRT) is a regimen for treating deficiencies in children and adults whose bodies, for one or more reasons fail to produce adequate somatropin (somatotropin, human growth hormone, hGH). This hormonal deficit contributes to poor growth and development in children, and in adults fails to maintain essential aspects of bodily form and function that are needed for a healthy life of normal duration.
The medical condition resulting from inadequate production and/or utilization of hGH is called growth hormone deficiency (GHD).5 Most cases are initially observed as an endocrine disorder in children that occurs equally in males and females, although males are often diagnosed more frequently.67 Because of its significant effect on growth and development as well as causing associated medical problems and reduced quality of life, childhood-onset GHD has been treated with replacement therapy for more than 30 years. In the past, hGH therapy in children affected by GHD was stopped at the time of epiphyseal closure (i.e. at final height). This focus on height originally reflected a measure of successful GH replacement therapy (GHRT) after which treatment was ended. This was done, in part because hGH was originally extracted from human cadavers making its supply fairly limited. However, with advances in technology it became possible to clone the gene capable of producing hGH. Thereafter, the recombinant form of human growth hormone (rhGH) became available in unlimited quantities. Because of its availability for clinical application, rhGH became and is now the drug of choice, not only because of its efficacy, but also because it avoids the risk of transmitting fatal, slow viral (prion-mediated) Creuzfeldt Jacob Disease which was sometimes associated with the cadaver-derived hormone.8 Although originally indicated for use in childhood GHD, rhGH became a licensed indication for GH-deficient adults in the United States, a number of European countries, and New Zealand in 1996. This action was taken because people who had been treated with rhGH as children and then routinely discontinued from treatment upon reaching final height, experienced higher than expected rates of medical problems as adults, beginning in their 30s and 40s. These included reduced physical, mental, and social energy, excess adipose tissue, diminished muscle mass, diminished libido, poor bone density, higher than normal cholesterol levels, and elevated rates of cardiovascular disease. Research trials soon confirmed that a few months of GH replacement therapy could improve nearly all of these parameters in GHD patients. Coincidentally, it was noticed that the same intrinsic diseases as well as maladaptive changes in form and function also occur spontaneously with advancing age.9
The progressive age-associated decrements in function of the GH neuroendocrine axis are collectively referred to as the somatopause. The term represents cessation of optimal secretion of somatotropin (hGH) which is analogous to declining production of reproductive hormones during the menopause and andropause in women and men, respectively. However, there are pathophysiological differences in childhood-onset and adult-onset GHD (AGHD) when compared with progressive, age-related GHD. Initial investigations into the causes of adult onset GHD showed them to result from damage to the pituitary gland due to tumors, surgery or radiotherapy that disrupted function of the GH neuroendocrine axis.1011 Since age-related GHD is not associated with the strict and exclusive acceptance of these originally defined, causal criteria for adult-onset GHD, nor is aging generally considered a “disease”, there was and continues to be reticence to diagnose GHD in the obese and in the elderly.121314 Thus at first, little attention was paid to the fact that as the body ages, progressive dysfunction of the GH neuroendocrine system results in clinical symptoms similar to those associated with factors originally recognized as causal for GHD.
For these reasons, administration of rhGH which is the accepted treatment for GHD, has not been permitted for use in aging by regulatory guidelines promulgated by the FDA. As a result, rhGH supplementation is not approved for medical treatment of the pathophysiologic, age-related decline in GH/IGF secretion, despite the clinical similarities with classically defined, adult-onset GHD. If used at all, lower doses are recommended in the elderly to reduce the incidence of side effects and maintain age-dependent normal levels of IGF-1. This is a confusing recommendation for the following reason. IGF-1 levels in normal young adults is higher than those in GHD adults. However, serum IGF-1 values in both groups are indistinguishable by the age of 40. Nonetheless, the declining values in “normal” aging people are not considered to be diagnostic criteria for GHD or GH insufficiency worthy of treatment with rhGH. Instead the range of laboratory reference values are shifted downward to reflect those in human subjects as they advance in age. Surprisingly, this is a unique practice which is not done for serum values of any other hormones. Nonetheless, it restricts in part, diagnosis of idiopathic GHD and treatment with rhGH to those under 40, and thereby requires different treatments for medical issues related to age-associated, GH insufficiency. To differentiate between classically defined adult-onset and age-related GHD associated with the somatopause, the latter is often called growth hormone insufficiency (GHI). Thus, because of the similarities between GHD resulting from trauma, disease or radiation from effects of aging that occur during middle and later stages of life, endocrine therapies for treating the latter condition have been sought over the past two decades.15 In fact many years of off-label use of sermorelin, a GH secretagogue, has improved the life and health of many suffering from progressively degenerative conditions of aging.
Many of the body’s systems that function to maintain optimal health and well-being decline with advancing age. Aerobic capacity, muscle mass, and strength all progressively decline with age. Loss of muscle mass, or sarcopenia, and the accompanying reduction in strength increases the risk of falls and their complications, and for many individuals the associated loss of physical, functional capacity leads to increasing difficulty in living independently. Complaints of poor sleep are common in older populations. Insomnia reduces quality of life and is often a factor in decisions to seek health care. Sleep complaints often lead to overmedication and sedation of the elderly, with the numerous potential attendant problems, including increased morbidity and mortality. Finally, cognition also declines with advancing age, particularly those cognitive functions that involve novel problem solving and psychomotor processing speed, with its own related impact on the older individual’s ability to function independently.16 Aging in both sexes is accompanied by profound decreases in GH output and in plasma IGF-I concentrations. This effect is separate from the alterations in body mass index that accompany the normal aging process. Attenuation of GH output associated with aging is related by inference to reduced GH-releasing hormone (GHRH) production, pulse amplitude as well as increased somatostatin (SRIF).171819
GH secretion rates decline exponentially from a peak of about 150 μg/kg/day during puberty to about 25 μg/kg/day by age 55.18 During this process there is a reduction in GH pulse amplitude, but little change in GH pulse frequency.20 There is a particularly marked decline in sleep-related GH secretion, resulting in loss of the nocturnal pulsatile GH secretion seen in younger individuals and lack of a clear night-day GH rhythm.2122 The decline in GH production parallels the age-related decline in body mass index and is associated with alterations in body composition, hormonal status, and functional capacity that mimic the changes seen in AGHD or partial hypogonadism.23 In addition to deteriorating memory and cognitive function, the changes in body composition that are most pronounced in normal aging include a reduction in bone density and in muscle mass and strength, an increase in body fat, and adverse changes in lipoprotein profiles.2425 While the aging pituitary remains responsive to GH, GHRH, and GH secretagogues, it is less responsive to stimuli such as exercise. This decline in GH production is initially clinically silent, but may contribute over time to sarcopenia and frailty. Since GH secretion declines progressively and markedly with aging, and many age-related changes resemble those of partial adult-onset GHD, stimulating production and secretion of endogenous GH with GH-releasing hormone (GHRH) or its analog Sermorelin, a GH secretagogue, could confer benefits in normal aging similar to those observed in AGHD. In particular, such treatment could reduce the loss of muscle mass, strength, and exercise capacity that leads to frailty; thereby prolonging the ability to live independently.
Growth hormone secretagogues (GSHs) are a class of molecules that stimulate the secretion of GH from the pituitary gland. They include agonists of the hypothalamic and pituitary ghrelin receptors (GHRPs, ipamorelin, hexarelin, etc.), and those of the pituitary GHRH receptor such as Sermorelin.
Sermorelin is a synthetic (man-made) version of naturally occurring GHRH that is produced in the brain and can be used clinically to stimulate release of growth hormone (GH) from the pituitary gland.26 Growth hormone is necessary for growth in children and is important in adults to maintain metabolic and physiologic functions that are necessary for good health and quality of life. Thus, Sermorelin can be effective in cases of GH insufficiency and thereby sustain essential bodily functions throughout life
Some uses for Sermorelin include: Diagnosis of growth hormone deficiency/insufficiency (GHD),27 treatment of children with idiopathic growth hormone deficiency,28 management of adult-onset growth hormone deficiency/insufficiency and other conditions requiring GH replacement therapy (GHRT),2929 regeneration of pituitary function and delay its functional decline during aging2830
Sermorelin is the most widely used member of the GHRH analogue drug class. It can significantly promote the synthesis and release of growth hormone (GH) from cells in the pituitary gland, improving the serum concentrations of GH and subsequently insulin-like growth factor 1 (IGF-1) in animals and humans.3132 It is able to influence the concert of hormonal signals that affect GH secretion from the anterior pituitary including GHRH, somatostatin, and insulin like growth factor (IGF) and others. The positive and negative opposing regulation of growth hormone by GHRH and somatostatin, respectively, creates a rhythmic-circadian pattern of GH secretion.33 Thus, modification of both pulse amplitude and frequency of GH secretion results from Sermorelin administration.34 After sermorelin stimulates the release of GH from the pituitary gland, it increases synthesis of IGF-1 in the liver and peripheral tissues.34
Sermorelin acts on the growth hormone releasing hormone receptor (GHRHr) in the pituitary to regulate cellular activities. GHRHr is the natural receptor for the endogenous hormone, GHRH, and for sermorelin. This receptor regulates growth hormone release directly by stimulation and indirectly by a feedback relationships with somatostatin.35
Sermorelin is readily degraded after reaching the bloodstream, having a biological half-life of approximately 10-20 min.36 Due to the biological half-life and bioavailability of Sermorelin, administration for growth in childhood GHD must occur periodically several times a day as subcutaneous-injections.37 However, single daily dosing is sufficient to treat most cases of adult-onset GH insufficiency. Three (3) mcg/kg subcutaneous-injections of Sermorelin have been reported to simulate a naturally occurring GHRH mediated GH release responses.38
In addition to increasing production and secretion GHRH also affects sleep patterns by increasing the amount of slow wave sleep (SWS) while augmenting sleep-related GH secretion and reducing cortisol secretion.39
To exert all its beneficial effects, Sermorelin requires a functioning pituitary and a host of peripheral tissues.4041 This is due to the reliance on endogenous receptors controlling hormone secreting glands and tissues. More precisely, functioning growth hormone releasing hormone receptors (GHRHr) are required on somatotrophs in a functioning anterior pituitary.40
Because of Sermorelin’s ability to bind receptors on somatotrophs, the pituitary cells that produce and secrete GH, sermorelin has several clinical indications and applications related to GHRH/GH insufficiency.42 For example it is officially indicated and approved for diagnostic evaluation of pituitary function and also for treatment of delayed or inadequate growth in children. It also can be used to oppose maladaptive changes in body composition such as reduced lean body mass (muscle), increased total and visceral fat, and decreased bone mass resulting from low or inadequate concentrations of serum GH and insulin-like growth factor-1 (IGF-1).
Data from research and clinical studies have demonstrated sermorelin’s multifaceted properties, some of which include:
- Peak increases in hGH followed administration of GHRH analogs after 15 or 30 min. An increase in the integrated plasma growth hormone (GH) response was observed at each dose.43
- Quality of life parameters including general well-being (P < 0.05) and libido (P < 0.01) significantly improved in men receiving sermorelin therapy.44
- Youthful concentrations and patterns of serum hGH were restored in older persons by daily injections of GRF (sermorelin).45
- Body composition improved after regular administration of GRF for 90 days resulting in increased muscle mass, increased total body water and decreased visceral fat.46
- Quality of sleep improved as indicated by extended Stage IV and Slow Wave Sleep in men.47
Symptoms of Adult Growth Hormone Deficiency/Insufficiency
Adults with inadequate concentrations of serum GH can have a variety of signs and symptoms, some of which include abnormal body composition, reduced fluid volume, diminished strength, physical energy and stamina, lack of motivation, lethargy, lability etc. Symptoms of growth hormone deficiency also depend on age, and often those meeting the classic definition of adult onset GHD can have different symptoms than a child similarly diagnosed. However, those with adult-onset GHD that are causally unrelated to aging have similar clinical symptoms as those that occur progressively in incidence and severity with advancing age.48
Diagnosis of Adult Growth Hormone Deficiency
Not everyone with growth hormone deficiency/insufficiency will have the same symptoms. Some people will only have one or two while others can have multiple symptoms. Fortunately, certain tests and exams can help physicians to make an appropriate diagnosis. Exams and tests used to diagnose growth hormone deficiency are the same no matter the patient’s age.
Diagnosing growth hormone deficiency typically starts with a physical exam. The physician checks weight, height, and body proportions. Other than a physical exam, there are many other tests and exams used to make a growth hormone deficiency diagnosis.
With respect to diagnosis of adult GHD of classical etiology, guidelines state that “adult patients with structural hypothalamic/pituitary disease, surgery or irradiation in these areas, head trauma, or evidence of other pituitary hormone deficiencies are considered appropriate for acquired GHD” and that “idiopathic GHD as which occurs during aging requires stringent criteria to make the diagnosis. The reason for this restriction is that as previously described, the age-related decline in function of the GH neuroendocrine axis is accepted as being a “normal” part of aging, even though it is progressively detrimental to many aspects of body function. Thus, due to the nature of the original diagnostic criteria for GHD, and the reticence to consider aging a “disease” per se, even though disease risk, incidence and severity can be attributed at least in part to declining activity of the GH neuroendcrine axis, the criteria for determining if secretagogue therapy is indicated as an intervention in aging, are less stringent than those promulgated by Endocrine Society guidelines.15
Some or all of the following tests can be used to diagnose age related GH insufficiency, since everyone will be so affected over the course of their lives. Such diagnostic testing may be used to determine the degree to which replacement therapy is indicated, i.e., for dosing determinations. Tests include:
Blood Tests for Growth Hormone Deficiency/Insufficiency
- Binding protein level (IGF-I and IGFBP-3) blood tests to determine whether or not the problem is caused by the pituitary gland
- Blood tests to measure the amount of growth hormone levels in the blood
- Blood tests to measure other levels of hormones the pituitary gland produces
- GHRH (Sermorelin)-arginine provocative test
- Other GH provocative stimulation tests
- Insulin tolerance test
Other Exams/Tests to Diagnose Age-unrelated Severe Growth Hormone Deficiency
In addition to blood tests, a physican may perform some additional exams and tests to help diagnose growth hormone deficiency. These may include:
- Dual-energy x-ray absorptiometry (DXA) scan to measure bone density.
- Brain MRI to examine the pituitary gland and hypothalamus.
- Hand x-rays (typically of the left hand) to examine the shape and size of bones which change as a person grows and ages. Bone abnormalities can be observed with x-ray examination.
- X-rays of the head can show any problems with the bone growth.
If an individual experiences signs and symptoms of GHD or GHI, he/she should talk to a doctor immediately so as to perform exams and tests that assist in making an accurate endocrine analysis and diagnosis.
Treatment of GHD
While aging is not a disease, it results in significantly maladaptive changes in body composition and function which affect the individual and the community at large. While aging is associated with a milder form of adult GHD, GH replacement with secretagogues such as Sermorelin has met with success. Once daily injections can stimulate increases in GH and IGF-I at least to the lower part of the young adult normal range.49 Because peptides like Sermorelin are readily destroyed by enzymes in the digestive tract, subcutaneous (sc) or intravenous (iv) injections are the only way to administer the molecule. Since iv injections are impractical for most people, the sc route is commonly used to administer doses of Sermorelin ranging between 0.2 – 1.0 mg per day. The most commonly used dosage is 0.5 mg daily. In a University of Washington study consisting of 6 months treatment with daily bedtime subcutaneous injections of Sermorelin, alone or in combination with supervised exercise conditioning, IGF-I levels rose approximately 35%. As with GH, subjects showed an increase in lean body mass and a decrease in body fat (particularly abdominal visceral fat).5051 Such changes indicate that regular GHRT with Sermorelin can resist changes in body composition underlying sarcopenia and frailty that lead to loss of independence. Thus, since the aging pituitary remains responsive to GH and GHS, it is reasonable that stimulation with Sermorelin is indicated in aging.52 While elders are more sensitive to GH, and thus more susceptible to the side effects of replacement with rhGH, stimulating production and secretion of endogenous GH with Sermorelin offers the advantage of a more physiological approach to increasing GH pulsatility while reducing risk for side effects.
Ipamorelin/CJC1295 Therapy in Washington, DC
What is CJC 1295 and its use?
CJC 1295 is a synthetically produced peptide that can increase your plasma growth hormone levels. CJC 1295 is usually injected into your body via a subcutaneous injection. CJC 1295 is also sometimes referred to as DAC:GRF. Stands for Drug Affinity Complex, and GRF stands for growth hormone-releasing factor. CJC 1295 can increase your IGF-1 levels and GH (growth hormone) levels in humans and in animals. DAC is added to this peptide in order to increase the half-life of CJC-1295. Initially CJC 1295 was developed to treat diseases and medical conditions for patients who had muscle disorders, diseases, and burn victims. CJC 1295 has drawn many individuals like athletes from around the globe for its incredible benefits and minimal side effects to enhance their performance on the field, and in the gym.
Benefits of using CJC-1295
Lean body mass, gains in muscle mass, and increased strength. These are just a few of the benefits which CJC-1295 will deliver upon. It is a long-acting GHRH analog or (growth hormone releasing hormone). The lifespan for releasing growth hormones is promulgated by tetrahedral modifications of CJC-1295, and the drug affinity complex (DAC). Therapeutic effects are increased because of this, and users require fewer injections in comparison to other growth hormones. These are just a few of the benefits CJC-1295 users will appreciate in comparison to other growth hormone injections available on the market.
Side Effects of CJC-1295
Of course many users will complain of side effects as it pertains to using supplements or injections. However, when it comes to CJC-1295 with DAC, the main CJC-1295 side effects are present as the growth hormone relates to the stimulation of the pituitary gland. An increase in vasodilation is often associated with the surge of the growth hormone into the user’s body. This typically lasts for a period of 30 minutes to 2 hours, post-injection.
Additionally, itching, pain, redness, and soreness are often noted as side effects at the injection point, although this is not reported with all users. HGH levels also increase at the cellular level once CJC-1295 is injected. Research suggests this can lead to: increased muscle strength, fat metabolism, and muscular mass. Improved skin-tone and muscle definition are also noted. For those who want to further enhance CJC-1295 with DAC effects will find that proper diet and exercise regimens will help in doing just that.
CJC-1295 Cycle: How should it be used/administered
Those who participate in studies for HGH often are given injections 2 to 3 times daily. This is typically before breakfast, before bed, and post-workout. These test periods can last up to several weeks in order to determine the actual CJC-1295 benefits on test-subjects. They are also meant to mimic as closely as possible, the actual secretion of the hormones.
The half-life of DAC is an 8 day period, and for this reason the cycles are usually shorter in duration. So the injections are only given once weekly, which result in increased GH secretion levels. Research currently doesn’t suggest that one or the other cycle delivers greater results, so it is a personal preference based upon what each user wants to use when injecting the CJC-1295.
GHRP and CJC-1295 Cycles
Growth hormone replacement peptides (GHRP 6) is typically used for synergistic effects, in conjunction with CJC-1295. For those on the weekly cycle, one evening injection of GHRP 6 is administered; this is done at night because it causes less of a cortisol surge, and prolactin, in comparison to GHRP 2. The GHRP 6 can also be used simultaneously with HGH cycles, 2 to 3 times daily, for a prolonged cycle, lasting several weeks.
Using CJC-1295 for Muscle Growth
Once adolescent growth ceases, it is difficult for the body to produce HGH in such high volumes as it did, making it harder to build lean muscle mass. HGH has helped in development of children who were deficient in the growth hormone, and this sparked a synthetic version to be created in 1985.
Several studies have since been conducted, detailing how HGH has helped build muscle mass, decrease body fat, and otherwise benefit adult users. Sometimes off-label prescription of HGH is given, particularly for athletes, the high cost, and difficulty to get a prescription, makes it otherwise difficult for adults who aren’t prescribed the injection, to be supplemented.
Research has shown that administering CJC-1295 once weekly helps to increase plasma GH concentrations (2-10 times more) for a period of up to 6 days after injection. Further, it increases IGF-1 levels by 1.5 to 3 times, for a period of 9 to 11 days, with no adverse side effects. For an athlete, those who are always on the go, or even moms who need a boost of energy, these injections can feel like users have found the “fountain of youth,” and will instantly notice a boost in energy levels.
Instructions for using CJC-1295
The injection is non-pyrogenic, sterile, and intended for subcutaneous or intramuscular injection use. It is to be administered after reconcentration with sterile water for injection purposes. An insulin syringe can be used for subcutaneous injection, with a 2 mg CJC-1295 dosage per injection. Per vial, a 1 X 2 ml injection is to be administered.
When using .5 ml of water for mixing, this provides 2 mg dosage (.50 ml or 50 units in one syringe). When using 1 ml of water, this equates to 2 mg dosage (1 ml or 100 units). The intended frequency is once weekly, with 2 mg dosage, due to the prolonged half-life.
Sample injections: Amounts to be administered
When using CJC-1295 it is important to follow proper dosage instructions. Depending on whether you are going to use the injection in the morning or evening hours, the frequency at which you will be injecting the syringe will differ.
CJC-1295 with DAC 600 mcg should be taken once weekly.
GHRP-2, GHRP-6 or Ipamorelin Example Injection:
A nighttime injection should be given on an empty stomach (best for use at night due issues with drowsiness). It should be taken 2-3 hours after your last meal.
You will inject the GHRP peptide and go straight to bed.
Example 2: Morning Injection:
You will inject 100 mcg first thing in the morning, and wait 20 minutes prior to consuming food or beverages (including coffee/water).
There really is no guesswork as it pertains to using the CJC-1295. Of course CJC-1295 dosage, and whether you use CJC-1295 without dac (or with), will determine when, and how you administer the GHRP.
CJC-1295 Reviews: Will this benefit me?
“Four months ago, I added CJC-1295 with DAC to my cycle.” The product is legitimate, andg it worked great for me!
“After including CJC-1295 with DAC, I leaned out, noticed greater muscle growth, and definition. What more could users ask for?”
“If you are looking for an alternative to HGH injections, you’ve found it with CJC-1295 with DAC. The product is far superior.”
In addition to these reviews, it is noted that CJC-1295 has helped increase blood serum levels, of HGH, within 3 to 11 days after inception of use. The longer half-life, alongside the continual release of growth hormone, means the CJC-1295 isn’t affected by food timing. This is contrary to other peptides you might’ve used in the past.
Using CJC-1295 with DAC
When you add DAC (drug affinity complex) to CJC 1295, you extend the half life of it by one week & it also helps you reach steadier blood levels after the injection. By adding DAC you also allow for the greater possibility of utilizing smaller Growth Hormone pules which was once thought of as a bleed, and when combined with a GHRP it can activate Growth Hormone stores the be released throughout the night at day. By stimulating cell growth, CJC-1295 will help improve skin-immunity, as well as internal organ-mass. Users further report that their sleep patterns are improved. This is essential to help in muscle development, and overall health.
The main purpose of CJC-1295 is to boost protein synthesis levels, and help fuel the growth of muscle tissues in the body. Many benefits will be derived by users who are incorporating CJC-1295 to their regimen; among these are:
- Reduced body fat.
- Quicker recovery times post-injury.
- Increased muscle mass.
- Increase in strength.
Using CJC 1295 Without DAC
If you are going to use CJC 1295 without DAC then you should know you are basically taking MOD GRF-129, which can be good for certain individuals that are looking to get shorter spikes of Growth Hormone release throughout the day. But if you are looking to not inject as much daily and still want to have a more powerful GH stores, then about 2- times a week you should choose to inject the CJC 1295 (with DAC). along with GHRPs that way you can reach the maximum potential of Growth Hormone release.
Will CJC-1295 cause water retention?
Because it stimulates the pituitary gland, those who are using higher doses of CJC-1295 might notice water retention in their body. Simply skip a dose, or reduce intake levels of sodium if you notice this issue. Water retention and increased levels of tiredness have also been reported by some users. After a couple of weeks, once the body has adapted, these issues typically resolve themselves. For those who notice these issues, it might be necessary to change your injection schedule, and only inject the CJC-1295 prior to bedtime, as opposed to in the morning hours.
CJC-1295 Proper Dosage
Modified GRF 1-29 (CJC-1295 without dac): 100 mcg per injection. Each vial contains 20 X 100 mcg doses.
Injection amount: If using 1 ml of water for 100 mcg dosage – use .05 ml per syringe when injecting. For 2 ml of water, .1 ml will be used per syringe.
Frequency: 1000 mcg should be injected 1 to 3 times daily, best if injected with 100 to 200 mcg of GHRP peptides.
CJC-1295 with DAC: Take 600 mcg once weekly, at any time.
Modified GRF 1-29 frequency: Inject 1 to 3 times daily, best when used with 100 to 200 mcg GHRP peptides.
How to inject CJC-1295
For best results, subcutaneous injections are suggested. Wash your hands and gather all materials, also clean the vial with alcohol prior to injection. Simply use an insulin syringe so you can extract the desired dosage, and tap/flick the syringe, so you can remove unwanted bubbles.
To prevent infection it is best to use an alcohol pad to wipe the skin prior to injection. Gently insert the needle into the fat, and inject the contents in the syringe. Once completed, wipe the injection site with alcohol, and dispose of the syringe.
CJC-1295 with Ipamorelin
CJC-1295 with DAC is often used alongside Ipamorelin because of the synergistic effects, and increased GH release levels. If you are on the CJC-1295 weekly cycle, you will include Ipamorelin evening injections (again, this may cause drowsiness). This will decrease cortisol and prolactin levels, in comparison to GHRP 2 and GHRP 6. You can also use Ipamorelin with stacked HGH, 2 to 3 times weekly, for prolonged cycles (as detailed above).
Research using Ipamorelin of 200 to 300 mcg dosage, 2 to 3 times daily with subcutaneous injections
It is best to begin with lower dosage, to reduce the side effects (typically rush/headaches). It is best to inject 20 to 30 minutes pre-workout, because of the pulse in growth hormone, it will produce the best results. Ipamorelin will work slower than GHRP, so spikes in GH levels isn’t as noticeable as quickly. The slower release is natural and has prolonged effects. Further, for those who are on restricted, calorie intake diets, there is no report of increased hunger levels using Ipamorelin or GHRP 6.
Is it normal to be flushed with CJC-1295?
Using 100 mcg per injection, most people respond well to the CJC-1295 injection. Head rush, or throbbing headache/pain, are the most commonly reported side effects by users upon administering the injection dosage. This may start 10 minutes post injection, and last for a period of up to 20 minutes.
This isn’t a serious side effect, and is attributed to the release of GABA (gamma-aminobutyric acid), which is a neurotransmitter. This is seen as a good/positive sign by users, as it indicates peptides are working, and HGH release is occurring in the body.
Is CJC-1295 better than HGH?
The answer is yes. Absolutely, CJC-1295 with DAC is far superior to the results you will experience in using HGH injections. The simple fact that CJC-1295 causes an increase in HGH levels and production, as well as stimulates production of IGF-1, are benefits most HGH products won’t produce.
As an added benefit, CJC-1295 is cheaper when purchased through Absolute Pharmacy than HGH supplements. You will also realize the same body fat loss levels, increased muscular development, and increases in natural strength.
Considerations when ordering CJC-1295
Regardless of the benefits you are trying to achieve, increasing growth hormone levels is beneficial to those who are working out routinely, and on a balanced diet. Not only will you realize an increase in muscle mass and lean mass development, you are also going to notice reduced body fat levels upon using CJC-1295 routinely.
Due to the nature of studies conducted, the usage and dosage each individual will administer, is up to them. It is important to however consider the fact that drowsiness, and headaches, are possible side effects to using the CJC 1295 with DAC. For this reason, it is important to test both nighttime use (once weekly), or morning use (2 to 3 times daily for a few weeks), to determine which works best for you.
The results you are going to see should be similar whether you are administering injections in the morning or evening hours. But, it is important to follow proper dosage instructions for safety, and for optimal results in muscle development, lean muscle mass, and to decrease body fat levels when incorporating CJC-1295 as a part of your diet and exercise regimen.
Increasing HGH release levels in your body naturally. It sounds too good to be true, but what if you could achieve just that by using a supplement? Using Ipamorelin alongside your exercise and diet regimen is going to help you achieve said goal. No two users are alike. For athletes or those who workout religiously, you might experience greater results than an individual who is overweight and just getting back into the gym after 10 years. So, take it with a grain of salt when detailing the results below. Dosage, your body composition, and other factors will play a role in the results you can expect to see when you incorporate Ipamorelin.
Now that you have an idea of what it can do for you, let’s delve into the dosage, possible side effects, proper use, and anything else you should know as a athlete, or individual who simply wants to naturally increase lean muscle mass, by introducing Ipamorelin into your system.
Ipamorelin is a growth releasing hormone; what this means is that if your body doesn’t produce enough, or if you are deficient, supplementing with Ipamorelin can help. It can be used as an alternative to GHRP-2 or GHRP-6. Users will experience similar results and gains, minus the documented side effects which are common with these two supplements.
200 to 300 mcg is typically the daily dosage which is recommended for the typical Ipamorelin user. It can be taken anytime during the day, but is advisable to be used in the morning, as it will help you achieve the best results in such cases. Regardless of when you start your dosage, it is important to ensure you are taking it at the same time each day. And, for new users, it is best to stick to a one-a-day cycle.
If you are a athlete, if you are used to working out regularly, or if you have already used the supplement in the past, it is possible that you can hike-up the recommended dosage levels. You can take the supplement 2-3 times per day, at the same 200-300 mcg dosage levels you would take with a single dose each day.
Ipamorelin Dosage Cycle
When you are just getting started with Ipamorelin, it is advised to use only one supplement daily at the same time each day. It is also advised to begin on the lower end, typically an eight week cycle, and at a maximum twelve week cycle. Doing this not only guarantees the desired results when using Ipamorelin, it is also going to ensure you get the most out of the supplement. When using at this dosage cycle you will:
- Increase muscle growth and development, and decrease body fat levels naturally.
- Realize an increase in energy levels throughout the course of your day.
- Natural increase in HGH levels, which is beneficial, as these levels dissipate naturally as you get older.
It does not matter what your intended use it; whether it is for weight loss, muscle mass development, lean muscle mass, or simply to increase HGH to their natural levels, you should always maintain the same dosage levels throughout the entire cycle. Do not increase use if you believe you aren’t achieving the results you are hoping for, as this can result in negative side effects, or lackluster results.
Timing Dosage: Why it matters
When taking Ipamorelin, you want it to be pushed through your system naturally, and at the same levels. If you are constantly altering the times you take it, or increase/decrease dosages during your cycle, this is not going to be attainable. To maximize the benefits and gains you are going to experience, dosage levels should be consistent, as should the timing of the dosage you are taking each day.
This can also potentially decrease the likelihood that you will experience adverse or negative side effects with use. It is also best to use your Ipamorelin injection when you are going to eat a meal; you won’t feel it, and it is easier to flow through your bloodstream when it is taken as such.
The Results: What Benefits Can I Expect?
As we mentioned above, the results you are going to realize are different for each user. A athlete might see immediate and greater gains, than a 50-year old male who has never stepped foot in a gym and is 30 pounds overweight. So, make sure you bear this in mind as you are determining whether or not Ipamorelin is right for you. Further, if incorporating other supplements like CJC 1295 or additional growth hormones, the results are also going to be greater than if you are simply using Ipamorelin on its own. Make sure you are aware of this, and how to properly incorporate it with other supplements, in order to ensure the best possible results with use.
Depending on the intended use, and your desired results, the dosage levels are going to vary from person to person as well. So, keep this in mind when trying to determine how great the results are actually going to be when you are using Ipamorelin. So, what exactly can you expect when using this supplement? Some things you will see, for every user is:
- An increase in growth hormone levels. These are naturally released by the pituitary glands, and as your body stops producing the hormone as you age, a supplement, such as Ipamorelin, can naturally help increase those dissipated levels.
- If using it with CJC 1295, you can experience a correlation in increased muscle mass levels. With longer release periods, greater results are achievable. So, if you want to gain more muscle mass, or if you simply want to increase levels of lean muscle mass, you are going to realize these possibilities when you incorporate the use of Ipamorelin into your daily regimen.
- Less downtime. You will recover faster, your body will recuperate faster, and you are back on your feet faster. So, you won’t experience as much downtime after a tough workout, letting you get back to your regimen faster.
- Faster weight loss is achieved. Increase in lean muscle mass, increase in metabolic rate, and increase growth hormones, all work together to help you burn more calories, and conversely lose more weight in less time.
- Your skin, nails, and hair will look better. It can work to help fight the signs of aging, and you are going to look and feel younger. A younger, more jovial appearance is almost instantly realized among users who incorporate Ipamorelin to their workout and diet regimen.
No growth hormone, or any supplement for that matter, is never going to equate to the same exact results for every user. So, what you experience, is not the same as the next user, and vice-versa. Further, the increase in results and how quickly you will see these results are going to differ for each user. So, make sure you understand this prior to starting your dosage, to ensure you are not disappointed if you do not see each one of these benefits, on the very first day that you begin using the Ipamorelin. Also consider the fact that if you use it after food, or with a meal, results will improve. So, proper timing, and proper diet and exercise regimen can greatly enhance the results you are going to realize when you are using Ipamorelin as well.
Cycling: How Should you take Ipamorelin?
An 8 to 12 week cycle is typically advised for new and for more experienced (repeat) users of Ipamorelin. If you are using it for the first time, it is advised to stick to a shorter 8 week period, to see how the results pan out, and also to determine if it is going to cause adverse side effects you experience.
This duration is a sufficient time to allow the ghrelin peptide to work through your system, and also for it to have a long lasting effect with continued use. It will work to enhance the hormone system, increase the metabolic rate, and increase lean muscle tissue levels in this period of time. As discussed above, the proper dosage for new users is 200 to 300 mcg daily, at the same time each day. For more experienced users, you can take the same dosage, 2 to 3 times a day (remember that it is the same time each day, and is best to use your injection after a meal for the best results possible).
Ipamorelin & Athletes: What benefits will you see?
As a athlete, incorporating a growth hormone like Ipamorelin is extremely beneficial. Not only in the development of lean muscle tissue and muscle mass, but also in the decreased recovery time you are going to experience after each workout. You can workout more, you can workout and lift harder, and you can increase your level of exertion at the gym to experience the greatest gains, as your body is going to heal much faster than it would without the growth hormone.
As a athlete, you can also increase your dosage cycle for a period of 12 to 16 weeks at a time, to maximize your gains. Do so gradually if you opt to go this route. Make sure you increase your daily dosage (1 to 2 doses per day, etc.) gradually. Start off with lower dosage levels as well, and see how it interacts with your body. You don’t want to experience withdrawal, nor do you want to exprience negative side effects when using Ipamorelin for longer dosage cycles. So, make sure you monitor your progress, see how you feel as you go, and make notes if/when you do experience negative side effects, so you can balance down to the proper dosage levels.
When you increase the dosage gradually it is also going to ensure you do not experience all (or any) of the noted side effects which are possible with the use of Ipamorelin. And, if you are taking other peptides, supplements, or growth hormones, it is the best way to ensure they are going to acclimate well, and work together well, in order for you to realize the greatest results possible when trying to increase muscle mass, and lean muscle tissue, without putting on body fat in the process.
Ipamorelin: First time user?
For those who are just getting started, make sure you go gradually. Start off with an eight week cycle, and start off with 200 mcg (rather than 300) per day. Doing a test run will allow you to see how your body is going to react. If all goes well, you can then increase your dosage cycle to an 8 to 12 week period, and possibly add an additional injection dose daily, or increase to 300 mcg with each use.
It is a trial and period session you will go through when you are new to Ipamorelin use. And, when you monitor use, properly incorporate it, and make sure you increase the dosage gradually, rather than all at once, it is going to ensure the best results, and the safest use, for new users to the supplement.
You’re not like the next person
It is also important to note that whether you are a long-time user, or a first-time user of Ipamorelin, your body is going to react differently to that of the next user. Like the benefits you will experience, the side effects you are going to experience will occur differently, and at different dosage levels. So, it truly is a trial and error period you are going to go through with a test run of Ipamorelin for new users. You have to find what works for you, how your body will react, and what potential side effects are lingering ahead, in order for you to achieve the greatest results, and eventually find the proper dosage and cycle level, which is going to work the best for your body and system.
Alternative Uses of Ipamorelin
There is no “one right way”, to use Ipamorelin. For example, if you are using 500 to 1000 mcg doses daily, twice a day, your cycle might run for an 8 week period. If on the other hand, you are a athlete training for a competition, you might be on 3 injections per day, at 300-500 mcg, and will stay on for a 12 week period. For new users, you might find a 300 mcg injection is too high, and you will cut back to 200 mcg until your body gets used to it, for an 8 week cycle.
You will learn that no single method of using Ipamorelin is right or wrong, and there is more than one route (and dosage cycle length) you can choose, when you do incorporate Ipamorelin into your diet and exercise regimen. Regardless of how high or how long the dosage cycle is, you want to start off on the lower end when you are new to using Ipamorelin, or any growth hormone for that matter. Not only will this reduce the potential risk of experience the side effects, it also ensures your body will ingest the highest levels into the bloodstream. And, it will allow you to gradually increase dosage and cycle lengths, in order to eventually get to the ideal levels which work best for your body, and for the intended/desired goals you are trying to achieve when using Ipamorelin daily.
Proper Use of Ipamorelin
When using Ipamorelin, you obviously want to use it properly. So, let’s go over a few of the ways in which you can use it, to achieve the best results.
With a blend of peptide and GH supplements, Ipamorelin can greatly help you in your weight loss endeavors. Using it with IGF-1 which is a natural growth hormone, can help you achieve even greater results. With lower dosage, you won’t increase muscle mass, your body will naturally decrease body fat levels, and you will begin to metabolize food faster, meaning you burn more calories in less time, for greater weight loss results.
Muscle mass gains
Athletes will greatly benefit from using Ipamorelin. For example, if you use CJC 1295 along with Ipamorelin, the results are going to be even greater. HGH increase will result in greater muscle mass levels, less time for muscle mass to develop, and increased levels of lean muscle tissue. The more peptides your body produces, the greater your lean muscle mass is going to be. And, over time, with gradual increases in HGH, you are going to realize a leaner, more muscular definition to your body.
If you suffer from anxiety, Ipamorelin can possibly help you reduce levels of anxiety as well. It can serve as a natural relaxant. It will help relieve and soothe the muscular system, so you will naturally feel a calming-effect when taking proper doses of Ipamorelin.
Ipamorelin can serve as a natural anti-aging solution. It is a growth hormone, and along with a peptide blend, can naturally help increase elasticity in the skin. Your nails, hair, and skill will look younger in no time at all.
Yes, Ipamorelin can help you lose weight. But, if you are not exercising, and aren’t eating well, it can only do so much. There is no magical supplement which will undo laziness and a horrible diet – keep this in mind. When using it for fat loss, make sure you are exercising. Doing so will naturally increase weight loss results, as you are going to burn more calories, along with the caloric deficit you are already on, for greater results. Further, your diet matters. If you are eating 5000 calories of junk per day, no supplement will help you lose weight – no matter how potent it claims to be!
Benefits & Possible Side Effects
We’ve gone through several benefits of using Ipamorelin; among these are:
- Weight loss in greater amounts and development of lean muscle mass.
- Muscle growth and development.
- Anxiety reduction, and improved appearance of skin (anti-aging formula).
Greater energy levels are also possible. Increasing growth hormones will naturally help add that “pep to your step” that you’ve lost. Remember, results will vary for everyone.
Some of the side effects you might experience will include:
- Increased cortisol levels – This is typically with higher doses and longer dosage cycles.
- Head rush/headache – This is often linked to higher dosage levels.
- Nausea/upset stomach – This might ensue in individuals who suffer from digestive issues, or when taken at higher dosage levels.
Speak to your doctor prior to use. They are the only one that can tell you if Ipamorelin is safe, and is proper for you to be using. Further, they will explain side effects, and what you should do in the event you do experience them.
Is Ipamorelin for me?
Weight loss, muscle growth, those who feel ‘depleted’, or if you simply want to increase loss of growth hormone production levels, Ipamorelin can help. If you fall into any of these categories, you are a candidate for use. You should still speak to your doctor prior to use. Not only will they explain possible complications or side effects, they will inform you of proper dosage, cycle, and how to use Ipamorelin.
Keep in mind the results will vary. Every user is going to experience different gains and benefits, at different levels. So, don’t compare your results to another user of Ipamorelin, as the results are not going to be the same.
BPC157 Therapy in Washington, DC
Adding supplemental boosters to your daily health routine has been the path many people have taken. Products such as protein powder, amino acids and pre workout compounds are just a few. Another group of supplements is called peptides. Peptides are essentially a chain of amino acids that benefit the body and its functions. Peptides are plentiful and have been shown to benefit a persons health, fitness and well-being. One of the newer peptides on the market is called BPC-157. BPC stands for body protective compound and studies have shown that this peptide does just that. This compound is actually derived from the gastric liquids found in the stomach. Research has shown BPC-157 to have considerable biological healing properties. In other words, it helps the body heal. It was originally developed to help heal inflammatory bowl disease and gastric ulcers. This makes sense since it comes from the stomach. This is not just a supplement for people with stomach issues.
Other studies when BPC-157 was used showed benefits for healing torn or damaged muscles, tendon to bone healing and general protection for our organs. Many people have successfully used this peptide to heal bleeding ulcers caused from NSAID overuse. This peptide can be very useful to athletes or just the average person who has daily aches or injury. Overuse of our body can cause muscle, tendon and ligament issues that affect our everyday life. The addition of BPC-157 can help heal the sore knees, pulled hamstring or sprained ankle. The most common and effective way to administer this peptide is by injection or transdermally. Fortunately a transdermal skin patch with BPC-157 is on the market ready to help with what ails you. Simply stick a patch on your arm, wrist or stomach and reap the rewards of this healing compound.
PT141 (Brem Therapy in Washington, DC for Men
PT-141 was developed from the peptide Melanotan 2, which is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis that is known as an alpha-Melanocyte stimulating hormone. PT-141 has been shown in studies to provide libido-enhancing effects by activating the melanocortin receptors MC1R and MC4R, without tanning the skin.
What is PT-141?
PT-141 was developed from the peptide Melanotan 2, which is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis that is known as alpha-Melanocyte stimulating hormone. PT-141 has been shown in studies to provide libido-enhancing effects by activating the melanocortin receptors MC1R and MC4R, without tanning the skin.
PT-141 is a potential remedy for the treatment of female sexual dysfunction and male erectile dysfunction.
Studies have shown that PT-141 does not act on the vascular system, but may increase sexual desire through the nervous system.
Patient Benefits Over Time May Include:
• Improves female sexual arousal disorder
• Improve sexual function in men (such as erectile dysfunction or impotence)
Typical Prescribing Protocol for Men:
Males with no history of ED may begin with 1mg (0.1mL) via subcutaneous injection in the lower right quadrant of abdomen at least 45 minutes prior to sexual activity (titrating dose upward to effect as needed or tolerated).
Males with a history or diagnosis of ED with inadequate response to Sildenafil 100mg may begin with 4mg (0.4mL) via subcutaneous injection in the lower right quadrant of abdomen approximately 45 minutes prior to sexual activity (titrating dose upward to effects as needed or tolerated).
PT141 (Brem Therapy in Washington, DC for Women
What is PT-141?
PT-141 was developed from the peptide Melanotan 2, which is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis that is known as alpha-Melanocyte stimulating hormone. PT-141 has been shown in studies to provide libido-enhancing effects by activating the melanocortin receptors MC1R and MC4R, without tanning the skin.
PT-141 is a potential remedy for the treatment of female sexual dysfunction and male erectile dysfunction. Studies have shown that PT-141 does not act on the vascular system, but may increase sexual desire
through the nervous system.
Patient Benefits Over Time May Include:
• Improves female sexual arousal disorder
• Improve sexual function in men (such as erectile dysfunction or impotence)
Typical Prescribing Protocol for Women:
Females with FSAD or HSDD may begin with 750mcg – 1mg (0.075mL – 0.1mL) via subcutaneous injection (titrating dose upward to effect as needed or tolerated) at least 45 minutes prior to sexual activity. Recommended to use no more than two times per week.
Side effects may include: nausea, flushing and headache.
Prostate Cancer Treatment: High Dose IV Vitamin C
High Dose IV Vitamin C:
At low concentrations Vitamin C is an antioxidant and protects against free radical damage which can lead to the development of cancerous cells. At high dosages, Vitamin C becomes oxidative and researchers have discovered that a highly-concentrated dose of vitamin C is “selectively” toxic to cancer cells, meaning the high dose of vitamin C harms cancer cells but not healthy tissue. Moreover, when this treatment is coupled with the addition of the enzyme catalase, the cancer-killing effect of the treatment was reduced significantly. This led researchers to believe that the high dose vitamin C infusion resulted in the production of large quantities of hydrogen peroxide, which initially caused a cancer killing effect that was then neutralized by the addition of the enzyme catalase. This suggested that cancer cells do not produce a sufficient amount of catalase to neutralize high levels of hydrogen peroxide on their own.
In fact, we now know that a large number of cancer cells produce small amounts of catalase in order to sustain low concentrations of hydrogen peroxide. This creates the cancer friendly environment of mild oxidative stress that encourages malignant cells to grow rapidly and become more aggressive. Fortunately for everyone, because a high proportion of cancers are only able to produce small amounts of catalase, they are very vulnerable to the cancer-killing effect exhibited by high levels of hydrogen peroxide.
The research at the National Institutes of Health has proven that in order to consistently achieve the concentration of vitamin C sufficient to provoke oxidation, a patient must receive dozens of grams of intravenous infusions of vitamin C. Oral administration is completely ineffective in this regard. A number of published case reports show that repeated high-dose intravenous vitamin C treatments yield objective tumor regression. These case reports are so compelling that intravenous vitamin C therapy is currently being formally evaluated in clinical trials at the NIH.
In theory, high-dose vitamin C therapy should not cause toxic damage to healthy tissue because the body produces sufficient amounts of catalase to efficiently neutralize the hydrogen peroxide produced. Our experience in the real world certainly supports the theory. We have treated hundreds of patients in this manner with no side effects. Our current protocol insures blood and tissue levels of vitamin C that are safe and effective to kill cancer cells.
Yet, a burning question still remains. Why hasn’t this therapy worked for everyone? There are three variables that can undermine the effectiveness of this therapy. First, some tumors produce larger amounts of catalase which neutralizes the oxidizing effect of hydrogen peroxide. Second, sometimes there are an insufficient number of catalysts to promote the transfer of electrons. Third, sometimes there is an insufficient amount of oxygen in the extracellular space, which is needed in order for vitamin C to produce hydrogen peroxide.
For now, scientists have not found a way to selectively block the production of catalase within tumors. However, we can definitively increase the effectiveness of this therapy by providing two supporting agents—electron transfer catalysts and tumor oxygenating agents.
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Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults
Context: Therapeutic use of GHRH to enhance GH secretion is limited by its short duration of action.
Objective: The objective of this study was to examine the pharmacokinetic profile, pharmacodynamic effects, and safety of CJC-1295, a long-acting GHRH analog.
Design: The study design was two randomized, placebo-controlled, double-blind, ascending dose trials with durations of 28 and 49 d.
Setting: The study was performed at two investigational sites.
Participants: Healthy subjects, ages 21-61 yr, were studied.
Interventions: CJC-1295 or placebo was administered sc in one of four ascending single doses in the first study and in two or three weekly or biweekly doses in the second study.
Main outcome measures: The main outcome measures were peak concentrations and area under the curve of GH and IGF-I; standard pharmacokinetic parameters were used for CJC-1295.
Results: After a single injection of CJC-1295, there were dose-dependent increases in mean plasma GH concentrations by 2- to 10-fold for 6 d or more and in mean plasma IGF-I concentrations by 1.5- to 3-fold for 9-11 d. The estimated half-life of CJC-1295 was 5.8-8.1 d. After multiple CJC-1295 doses, mean IGF-I levels remained above baseline for up to 28 d. No serious adverse reactions were reported.
Conclusions: Subcutaneous administration of CJC-1295 resulted in sustained, dose-dependent increases in GH and IGF-I levels in healthy adults and was safe and relatively well tolerated, particularly at doses of 30 or 60 microg/kg. There was evidence of a cumulative effect after multiple doses. These data support the potential utility of CJC-1295 as a therapeutic agent.
Typically, there are two ways to boost levels of HGH in the body. The first is by using a growth hormone releasing hormone (GHRH) or growth hormone releasing peptide (GHRP) and the second is by using actual HGH.
Growth Hormone Releasing Hormone/Peptide Therapy
Sermorelin, Tesamorelin, Ipamorelin, MK-677 and CJC 1295 are all releasing hormones and peptides that stimulate the pituitary gland to produce and secrete HGH. They can increase the volume of human growth hormone (HGH) secreted by the pituitary gland. This treatment is prescribed for use in adults to increase lean muscle mass, reduce body fat, increase bone density, enhance the immune system, and strengthen the heart and other organs of the body. Since the increased volume of human growth hormone is produced by the body's pituitary gland, the body's endocrine system will not allow more growth hormone to be produced by the stimulation of the pituitary than the body can safely process within the endocrine self-monitoring system. Its use for adult hormone deficiency is not restricted.
Ipamorelin, a growth hormone releasing peptide, can be added to Sermorelin. CJC 1295 can be added to Ipamorelin. Both act the same but on different receptors. A combination of both can increase the effectiveness and overall outcome of treatment.
Actual Human Growth Hormone Therapy
Actual HGH can also be used directly to boost levels of growth hormone. By using actual human growth hormone you bypass the pituitary gland. This allows you to take advantage of the benefits of HGH much sooner with higher doses. Positive results are achieved much quicker with this approach.
Studies have shown that the fastest and most effective way to manage the signs and symptoms of aging, such as decreased libido, lack of energy, weight gain or difficulty losing weight, decreased mental alertness, weakened immune system is to boost your growth hormone levels. To get the best of both worlds therapy can consist of bioidentical HGH injections providing an instant boost of human growth hormone in your body, and a growth hormone releasing hormone prompting your pituitary gland to produce its own human growth hormone to sustain these benefits over the long term. This is a very powerful combination therapy which prevents essentially all of the side effects of HGH therapy alone. Growth hormone releasing hormones and HGH treatment combined provide more of the benefits than available from either program by itself.
IGF-1 Therapy (Insulin-like Growth Factor)
IGF-1 is a naturally occuring protein with a molecular structure similar to insulin. It is not Human Growth Hormone. Rather, it is produced inside the body primarily by the liver as an endocrine hormone, and functions as a mediator of the effects of growth hormone. When growth hormone is released into the blood stream from the pituitary or from an injection, it stimulates the liver to produce IGF-1, which in turn stimulates growth in a broad range of cells: skeletal, muscle, cartilage, bone, nerve, skin and multiple organs. In fact, the majority of the benefits related to HGH are actually brought about as a result of IGF-1 and other growth factors. IGF-1 and HGH treatment combined provide more of the benefits than available from either program by itself.
To learn more about your growth hormone therapy options and the results therapy can produce, call 480-839-4131 to schedule a consultation with one of our licensed physicians. You may also request a consultation using the consultation request form located throughout the site.
All patients always work directly with one of our licensed physicians to ensure patient safety and confidentiality.
It is important to remember that any program or treatment we offer at Transformyou carrying the phrase 'Anti-Aging’ is not intended to stop or prevent one from aging. Rather, our services and products are designed to help individuals effectively manage and navigate the aging process, yielding the best possible levels of health and wellness.
Hgh vs cjc 1295
CJC-1295 is a synthetic peptide which acts as a growth hormone secretagogue. CJC-1295 is also referred to as DAC:GRF, this stands for drug affinity complex: growth hormone releasing factor. CJC-1295 is a growth hormone (GH) and insulin-like growth factor 1 (IGF-1) releasing peptide with a long half-life. Administration of CJC-1295 is an incredibly effective method to increase the natural release of GH and elevate IGF-1 levels.
What is CJC-1295?
CJC-1295 is a synthetic analogue of the naturally occurring peptide, growth hormone-releasing hormone (GHRH) also known as growth hormone-releasing factor (GRF). CJC was developed by CONJUCHEM Biotechnologies Inc. GHRH is a 44 amino acid peptide which is required for the natural pulsatory secretion of GH; amino acids 1-29 are responsible for its biological activity. Exogenous application of Growth Hormone is associated with several negative side effects and it is believed that these side effects can be circumvented by using growth hormone secretagogues such as GRF. This is because of the growth hormone secretagogue’s more natural pulsatory release of GH. However, GRF has far too short of a half life to see clinically relevant elevations in GH and IGF. CJC-1295 was derived from the modification of GRF1-29 and selected for further research due to its long half-life. CJC provides the natural pulsatory release of GH and IGF-1 like GRF, but for longer periods of time which makes it a great candidate for therapeutic use.
CJC-1295 is GRF1-29 with a modification to four amino acids. This prevents biological degradation of the peptide. This is done by resisting proteolytic cleavage by proteolytic enzymes like dipeptidyl peptidase-4 (PPD-4), which is known to cleave growth factors. The modification to the four amino acids is know as Drug Affinity Complex TM (DAC). DAC is a peptide drug technology developed by CONJUCHEM Biotechnologies Inc. DAC modifies 4 amino acid positions that will still allow for biological activity of the original peptide, while preventing cleavage. Maleimidopropionoic acid is bound to the peptide via lysine which binds the free thiol of cycsteine-34 in albumin. The binding of the peptide in albumin creates a much longer and sustained effect of the drug. Due to this technology the half-life of CJC-1295 is 8-10 days in humans. (1,2,3)
CJC-1295 causes significant increases GH and IGF-1 so it will provide the same benefits found with the use of these growth factors. Healthy adults deficient in Growth Hormone can benefit in the following ways:
· increased exercise capacity
· increased muscle mass
· increased bone density
· decreased body fat
CJC-1295 Side Effects
CJC-1295 has been tested in humans with relative safety and effectiveness. S. Teichman et. Al conducted two randomized, double-blind, placebo-controlled studies. 66 Healthy adults, 21-64 years of age were administered subcutaneous CJC-1295. The peptide was dosed at 30-125 ug/kg of bodyweight, 1-3 times weekly or bi-weekly, for 28 and 49 days. The compound was most well tolerated at 30-60 μg/kg of bodyweight. There were no serious adverse events reported, most common side effect was injection site irritation. Other side effects included headache, diarrhea, and vasodilation. The study found a dose dependent increase in GH and IGF-1 levels. GH was increased 125% and IGF-1 was increased 80% for up to 6 days by just one single injection! M. Lonescu et. al assessed GH pulsatility of 20 healthy men ages 20-34 after a single injection of CJC-1295. Researches found a 40% increase in GH as opposed to an expected 75% increase, with no significant difference being found between a 60 μg/kg and 90 μg/kg doses. The natural GH pulsatility was maintained which dispels the “GH bleed” myth commonly mentioned in reference to this compound. This study found “no serious adverse effects,” most common side effects were increase in heart rate and injection site irritation. All side effects were short in duration.
During ConjuChem’s Phase II clinical trial of 192 subjects, a patient receiving their second to last CJC injection of the trial complained of chest pains two hours after injection. The patient underwent a ECG which identified a myocardial infarction, death occurred one hour later. ConjuChem’s states as follows:
“There is no evidence of any cardiotoxic effects of DAC(TM):GRF in previous preclinical or clinical studies. The attending physician stated that his most likely explanation for the event was the patient had asymptomatic coronary artery disease with plaque rupture and occlusion.”
Their conclusion was the death of the participant was due to preexisting heart issues. (4,5,6)
CJC-1295 vs HGH
CJC-1295 has several advantages over exogenous HGH application. The most profound benefit is that CJC only requires administration once per week, this makes ease of use much greater. CJC stimulates natural release of GH and maintains the natural pulsatory nature of GH release in the body. This may reduce or avoid the common side effects associated with HGH use. Although this suggests CJC-1295 would be a better choice than HGH, I do believe that an athlete like a pro bodybuilder seeking a super human physique may be able to elevate GH and IGF-1 much higher with exogenous HGH. However, these levels may be able to be duplicated with the stacking of CJC along with other peptides.
CJC-1295 is commonly used in bodybuilding, fat loss, and life extension circles. Most conversation about and anecdotal accounts of CJC use take place on bodybuilding forums. This compound has not been approved by the FDA , therefore it is important to note that safety and dose have not been established for human use. CJC-1295 dose has been reported in a range of 0.1-10mg per week. The average reported doses seem to start at around 2mg with users ramping up to 6-8mg. The clinical research I cited used 30-125 μg/kg, this translates to 6-25 mg per week in a 200 lb person. These doses were well tolerated with little difference in results above 60 μg/kg.
CJC-1295 Doping and Detection
The detection of CJC-1295 administration has been shown in animal models via immunoassay methods. I was unable to find any accounts of qualitative detection in human competitive athletes. The reports of CJC-1295 use in sport have seemingly been accusations or evidential. However, there are reports of positive secretagogue PED tests for Ibutamoren, Ipamorelin, GHRP-6, and GHRP-2. (7,8)
CJC-1295 is readily available to purchase for research purposes only, as it is not approved for human use. Typing said compound right into your search bar will provide you with many vendors to purchase this compound from.
1. Lucie Jetté, et al. July 2005. Human Growth Hormone-Releasing Factor (hGRF)1–29-Albumin Bioconjugates Activate the GRF Receptor on the Anterior Pituitary in Rats: Identification of CJC-1295 as a Long-Lasting GRF Analog. Endocrinology. Volume 146 (Issue 7). https://doi.org/10.1210/en.2004-1286
2. Maria Alba, et al. December 2006. Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse. APS Endocrinology and Metabolism. Volume 291 (Issue 6). https://doi.org/10.1152/ajpendo.00201.2006
4. Sam L. Teichman, et al. March 2006. Prolonged Stimulation of Growth Hormone (GH) and Insulin-Like Growth Factor I Secretion by CJC-1295, a Long-Acting Analog of GH-Releasing Hormone, in Healthy Adults. The Journal of Clinical Endocrinology & Metabolism. Volume 91 (Issue 3)
5. Madalina Lonescu, et al. December 2006. Pulsatile Secretion of Growth Hormone (GH) Persists during Continuous Stimulation by CJC-1295, a Long-Acting GH-Releasing Hormone Analog. The Journal of Clinical Endocrinology & Metabolism. Volume 91 (Issue 12)
CJC-1295 is an incredibly effective growth hormone and works by causing another substance to be secreted. It stimulates the release of your own body’s growth hormone which. Research show that after the age of 30 the body’s growth hormone level drops quickly and approximately 15% every 10 years. CJC-1295 is able to increase growth hormone naturally by binding to receptors for growth hormone releasing hormone (GHRH) on your brain and more specifically the pituitary gland. By doing this it triggers the brain to release growth hormone that would have otherwise been lost with age. Research completed with healthy men and women between the ages of 21 and 61, showed that CJC-1295 had the ability to increase serum growth hormone levels by 200-1000%. In these individuals, the elevated growth hormone production and release continued for up to 6 days because CJC-1295 has a half life of about 6-8 days. This longer half-life means the body continues to produces beyond the day of injection and is thought to be a great benefit has compared to other peptides that also have similar actions. For this reason and a few more, CJC-1295 has become very effective peptide for safely increasing growth hormone levels.
CJC-1295 is safely biologically increased growth hormone levels without the side of effects of other medication such hGH treatment which have been none to have more side effects. Some of the side effects of CJC-1295 are generally mild and tend to not last long if at all such as headache, flushing, and dizziness. The most common reported side effect is redness and irritation at the injection site.
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Most People Have No Idea How Good Their Bodies Are Designed To Feel
The Ultimate Peptide Duo: CJC1295 and Ipamorelin. At AURA BODY, our goal is to lead the wellness industry with medical-grade, quality peptide treatments to get you your BEST results. We now have the technology to create peptides to bind very specific receptors in our body to achieve a specific outcome.
Body by Aura’s Aura Advanced peptide therapy is a combination of CJC 1295 and Ipamorelin. CJC 1295 (GHRH) increases the amount of Growth Hormone your body reduces and Ipamorelin (GHRP) stimulates the release of Growth Hormone. These two peptides work together to restore your body’s Growth Hormone levels.
Our natural GH levels decline drastically as we age. Unless it is naturally optimized, it will continue to decline, bringing all the signs and symptoms of aging along with it. https://www.auramdbody.com/aura-peptide-therapy/
How is Peptide Therapy Any Different from HGH Therapy?
HGH (Human Growth Hormone) Peptides like CJC1295 and Ipamorelin don’t replace your body’s own growth hormone production. In contrast, they naturally increase your body’s own production of growth hormone.
This is a far cry from human growth hormone injections because direct HGH therapy halts your body’s own production of growth hormone altogether! Finally, to make things even worse with direct HGH therapy, it will cause a complete imbalance of other hormones in your body which typically is what causes the unwanted side effects like carpal tunnel syndrome, enlarged breasts in men, liver damage, and even cancerous tumors.
What Are The Benefits of CJC1295 and Ipamorelin?
There are many benefits to CJC 1295 and Ipamorelin. Studies have shown that the results are safe and therapeutic for healthy adults. Some of the amazing benefits for CJC 1295 and Ipamorelin are:
- An Increase in Lean Muscle Mass
- A decrease in Body Fat Percentage
- Significantly increased Collagen, elastin and fibrin production
- Increased Restful Sleep Stages naturally (Stages III and IV)
- Increase in Energy Levels
- Enhanced Libido
- Improved Cardiovascular Function
- Heightened Immunity
- Decreased Joint and Muscle Pain
- Enhanced Healing after Injury
Don’t wait to find out even more about Peptide Therapy and the Aura Advanced formula. Call us today or schedule online and start looking and feeling your best with this amazing science.