CJC-1295 is a synthetic GHRH analogue modified with Drug Affinity Complex (DAC) technology — a maleimide group that covalently binds albumin in the bloodstream, extending half-life from minutes (native GHRH) to 6–8 days. In a Phase II human clinical trial by Teichman et al., a single injection produced 2–10 fold GH elevation and 1.5–3 fold IGF-1 elevation maintained for 6 days — establishing it as the most studied sustained-release GHRH analogue.
For in vitro laboratory research use only. Not for human consumption. All findings described are from preclinical or in vitro models.
In vitro and preclinical mechanistic observations
Binds GHRH-R on pituitary somatotroph cells, stimulating GH gene transcription and secretion through the same pathway as endogenous GHRH.
The maleimide group covalently binds lysine residues on circulating albumin, creating a GH-release depot with a 6–8 day circulating half-life.
GHRH (CJC-1295) and ghrelin mimetics (ipamorelin) act on different receptors synergistically — together producing GH release far greater than either alone.
Drives sustained hepatic IGF-1 production lasting the full week between injections — enabling consistent downstream anabolic and regenerative signaling.
Quantitative findings from published preclinical research
GH fold-increase over baseline. Source: Teichman et al. (2006) J Clin Endocrinol Metab. PMID 16822960.
Observed tolerability data from in vitro and animal model research
Tolerability
Low SeverityTransient Flushing
Low SeverityWater Retention
Low SeveritySafety data reflects preclinical observations only. Human clinical safety profiles may differ substantially. For in vitro laboratory research use only. Not for human consumption.
Primary literature — links open PubMed or original journal source
Syntra Compound Library
View CJC-1295 specifications, batch data, and Certificate of Analysis in the Syntra research compound catalogue.
View CJC-1295 in the Syntra Compound Library →For in vitro laboratory research use only. Not for human consumption.
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