Physician PracticeResearch Use OnlyWADA Prohibited

CJC-1295

A GHRH analog studied for GH axis stimulation and body composition research. Available in two pharmacokinetically distinct forms — no-DAC (short-acting) and DAC (long-acting). Protocols differ significantly between variants.

PerformanceGH AxisGHRH AnalogInjectableno-DAC / DAC
QUICK FACTS
CLASSGHRH analog (Mod-GRF 1-29 / CJC-1295)
MOLECULAR WEIGHT~3,368 g/mol (no-DAC)
MECHANISMGHRH receptor agonist — pituitary GH stimulation
KEY DISTINCTIONno-DAC (t½ ~30 min) vs DAC (t½ ~6–8 days)
EVIDENCE STATUSInvestigational / physician practice
WADA STATUSProhibited
Overview

CJC-1295 is a synthetic GHRH analog that stimulates the pituitary gland to release growth hormone by activating GHRH receptors. It is available in two pharmacokinetically distinct forms that require completely separate protocols: CJC-1295 without DAC (also called Mod-GRF 1-29), which has a short half-life of approximately 30 minutes, and CJC-1295 with DAC, which binds albumin in the bloodstream for a half-life of approximately 6–8 days.

The no-DAC variant is the more commonly used form in physician practice for body composition protocols. Its short half-life allows for pulsatile administration aligned with natural GH rhythms, typically dosed daily in the AM fasted state. The DAC variant produces sustained GH elevation with less frequent dosing, but its prolonged action carries different considerations for GH feedback and IGF-1 elevation.

In physician practice, CJC-1295 no-DAC is almost always paired with Ipamorelin. The combination uses two complementary mechanisms — GHRH receptor stimulation (CJC-1295) and ghrelin receptor stimulation (Ipamorelin) — to produce a synergistic GH pulse that significantly exceeds what either compound achieves alone.

Research Areas
GH axis stimulationGHRH receptor researchBody composition researchIGF-1 modulationPulsatile GH release (no-DAC)Sustained GH release (DAC)
Available Evidence3 categories
HumanPhase I/II studies demonstrated GH and IGF-1 elevation. Limited controlled data in healthy athletes. Physician practice predominates for non-GH-deficiency body composition applications.
In VitroReceptor binding confirms GHRH agonist activity. DAC conjugation chemistry studied for extended half-life via albumin binding mechanism.
UncertainOptimal no-DAC vs DAC protocols, long-term safety, and body composition effects in healthy populations not established in RCTs.
Documented Research Benefits6 documented
GH pulse stimulation
human
IGF-1 elevation
human
Body composition support
physician practice
Lean mass research
physician practice
Sustained release (DAC)
pharmacokinetic
Pulsatile release (no-DAC)
pharmacokinetic
Research Pairings3 common
Ipamorelin
Defining pairing. GHRH + GHSR dual mechanism produces synergistic GH pulse amplification — the standard performance GH axis stack in physician practice.
View Ipamorelin →
Tessa
Both are GHRH analogs — do not combine. Choose one GHRH agent per protocol.
View Tessa →
Serm
Also a GHRH analog — do not combine. CJC-1295 generally preferred when both are available due to its slightly longer half-life.
View Serm →

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Safety & Regulatory Status

CJC-1295 is not FDA-approved and is prohibited under WADA. Research use only. Critical: no-DAC and DAC variants are not interchangeable — verify the exact variant before applying any protocol.

Side effects include water retention, joint aches, and transient numbness consistent with GH elevation. Long-term safety in healthy adults not established. All information for educational reference only.

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