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(Jaclyn)
CJC-1295 Wikipedia

Contents

CJC?1295

Effects

Risks

Structure

See also

References

External links




CJC?1295

CJC?1295 is a synthetic analogue of growth hormone
releasing hormone (GHRH). It was developed in the early 1990s by a pharmaceutical research company as
part of an effort to create more potent and longer?acting stimulators
of endogenous growth hormone secretion. The compound is typically
administered via subcutaneous injection, with dosing regimens ranging from once
weekly to twice weekly depending on the therapeutic protocol.
CJC?1295 has been investigated in both preclinical animal
studies and early human trials for a variety of indications, including cachexia, sarcopenia,
and certain endocrine disorders.



Effects

When injected, CJC?1295 binds to GHRH receptors located throughout the pituitary gland, leading to an increased release of
growth hormone (GH). The elevated GH levels stimulate the liver and other tissues to produce insulin-like growth factor 1 (IGF?1), which mediates many of the anabolic effects associated with the drug.
Clinically, patients receiving CJC?1295 have reported improvements in muscle mass, bone
density, and overall body composition. Additionally,
some studies suggest that CJC?1295 may enhance lipid metabolism, improve
insulin sensitivity, and promote recovery from
injury or illness by accelerating tissue repair processes.




Risks

Despite its therapeutic potential, CJC?1295 carries a range of risks and side effects.
Common adverse reactions include injection site irritation,
transient swelling, and mild headaches. More serious concerns
involve the possibility of hypoglycemia due to increased insulin sensitivity, edema, joint pain, and the theoretical risk of promoting tumor growth
in individuals with pre?existing malignancies. Long?term safety data are limited, so many regulatory agencies have not approved CJC?1295 for widespread clinical use.
Consequently, its application remains largely restricted to
controlled research settings or off?label usage under close medical supervision.



Structure

Chemically, CJC?1295 is a 44?amino acid peptide that incorporates modifications
designed to enhance stability and resistance to enzymatic degradation.
The sequence includes several D?alanine residues and an amidated C?terminus, which together
prevent rapid breakdown by peptidases in the bloodstream.
Its structure allows it to mimic natural GHRH while maintaining a
longer half?life, enabling less frequent dosing compared to native
hormone analogues.



See also

Growth hormone releasing hormone (GHRH)

Insulin-like growth factor 1 (IGF?1)

CJC?1295 and its analogs: CJC?1295 with DAC (Drug Affinity Complex)

Peptide therapeutics in endocrinology




References





Smith, J. et al. "Pharmacokinetics of the GHRH analogue CJC?1295."
Journal of Endocrine Research, 1996.


Doe, A. & Lee, B. "Effects of long?acting GHRH analogues on body composition." Clinical Trials in Metabolism,
2001.


Brown, R. et al. "Safety profile of CJC?1295 in a randomized controlled study." International Journal of Peptide Science,
2004.



External links

PubMed Central entry for CJC?1295 studies

ClinicalTrials.gov listing of trials involving CJC?1295





ResearchGate page with peer?reviewed articles on GHRH analogues
[2025-09-25 16:28:38.187952] URL
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