CJC-1295 with DAC
/ Modified human GHRH(1-29) analog with drug-affinity-complex (DAC) maleimide group for covalent albumin bindingALIAS · CJC-1295 DAC · Long-acting GHRH analog · CJC-1295(DAC) · GHRH(1-29)-DAC
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Tier 4 in current literature. The original Phase 1 work (Teichman 2006) showed pharmacokinetic proof-of-concept for a once-weekly long-acting GHRH analog via covalent albumin binding (DAC technology). No Phase 2 or Phase 3 development continued; not approved anywhere.
CJC-1295 is a modified GHRH(1-29) analog with a maleimidopropionyl linker (the 'DAC' — drug affinity complex) that forms a covalent bond with serum albumin in vivo. Albumin binding extends the half-life from minutes (native GHRH) to roughly one to two weeks, producing sustained GHRH receptor stimulation at the somatotrope and elevated mean GH and IGF-1 levels.
Tier 4. A single 2006 Phase 1 single-ascending-dose study in healthy adults demonstrated dose-dependent IGF-1 elevation lasting up to 28 days post-injection. No Phase 2 or Phase 3 trials of CJC-1295 with DAC have been published.
Phase 1 reported injection site reactions and transient flushing; small sample size and short follow-up cap the safety database. Sustained GH/IGF-1 elevation over months has not been characterised in humans.
Regulatory status
- FDA status:
- Not FDA-approved
Marketed by research-chemical vendors with claims of weekly dosing, but the published human PK data come from one Phase 1 study by the molecule's developers (ConjuChem). Independent replication, long-term outcomes, and Phase 2/3 efficacy data do not exist. Vendor product purity and identity vary.