Overview
CJC-1295 no DAC / Ipamorelin is a short-pulse GH-axis stack. It combines a short-acting GHRH-side analog with Ipamorelin's ghrelin/GHS-receptor signal to organize discrete GH-release windows. [1][2][5][6]
The practical reason for the stack is timing control: both components can be placed around short GH-pulse windows instead of sustained exposure. That timing logic does not establish the stack for recovery, fat loss, sleep, or longevity outcomes. [2][8]
Peptides in this stack
CJC-1295 (no DAC)
GH/IGF axis peptide
A short-acting GHRH analog used for pulse-oriented GH-axis signaling, with indirect human support and limited direct no-DAC outcome evidence.
Ipamorelin
GH/IGF axis peptide
A selective ghrelin-receptor secretagogue with human GH pharmacology and postoperative GI trial data, but limited long-term wellness outcome evidence.
Why They're Combined
CJC-1295 no DAC is included for short GHRH-side pituitary signaling, while Ipamorelin is included for ghrelin/GHS-receptor stimulation. The combination is common because each compound pushes GH release through a different upstream route. [1][2][5][6]
No-DAC timing is the point. The stack is used to create short, repeatable release windows rather than long background stimulation. That makes timing, meals, sleep, and training context part of the protocol logic. [2][3]
How They Work Together
The proposed mechanism is a coordinated pulse: a GHRH-side signal primes pituitary GH release while Ipamorelin activates the secretagogue receptor side. Pairing them is meant to create a more organized pulse than either signal alone. [1][2][6]
Because the stack still feeds the GH/IGF-1 axis, the downstream monitoring issues stay in the same family: IGF-1, glucose, edema, numbness or tingling, sleep quality, and anti-doping status. Shorter action does not remove those considerations. [8][9][10]
What the Evidence Shows
The no-DAC rationale leans on human GHRH(1-29) and D-Ala2 GHRH pharmacology plus Ipamorelin component data. Those sources support receptor and timing logic more than real-world outcome claims. [1][2][6]
No controlled human trial establishes that no-DAC CJC-1295 plus Ipamorelin improves sleep, recovery, fat loss, lean mass, or aging outcomes. Treat the stack as pulse logic with incomplete outcome evidence, not a proven recovery or body-composition protocol. [8][7]
Typical Protocol
Common no-DAC stack pulses use Modified GRF 1-29 at 100-200 mcg with Ipamorelin at 200-300 mcg per administration. Bedtime is the most common anchor, with some schedules adding a morning or post-workout pulse away from heavy meals. [2][6][8]
Common cycle structures are daily dosing or 5-days-on, 2-days-off for 8-12 weeks before symptoms and labs are reviewed. The main practical rule is consistency: changing dose, timing, meals, and training in the same week makes the stack hard to read. [8][7]
Important Considerations
This stack is often confused with CJC-1295 DAC / Ipamorelin. Keep them separate: no-DAC is pulse-oriented, while DAC is longer acting and carries different exposure assumptions. Food timing, pulse spacing, and missed doses matter more with the no-DAC version. [2][3][4]
Product quality and dose precision matter because small microgram mistakes can change the effective pulse. IGF-1, fasting glucose, edema, numbness or tingling, sleep quality, and blood pressure are practical review points. Tested athletes should treat GHRH analogs and GH secretagogue stacks as anti-doping risk areas. [9][10][8]
Published research 10 sources
Growth hormone responses to growth hormone-releasing hormone (1-29)-NH2 and a D-Ala2 analog in normal men.
PubMed / Peptides, 1985. human clinical.
Incorporation of D-Ala2 in growth hormone-releasing hormone-(1-29)-NH2 increases the half-life and decreases metabolic clearance in normal men.
PubMed / Journal of Clinical Endocrinology and Metabolism, 1994. human clinical.
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.
PubMed / Journal of Clinical Endocrinology and Metabolism, 2006. human clinical.
Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog.
PubMed / Journal of Clinical Endocrinology and Metabolism, 2006. human clinical.
Ipamorelin, the first selective growth hormone secretagogue.
European journal of endocrinology, 1998 Nov. review.
Pharmacokinetic-pharmacodynamic modeling of ipamorelin, a growth hormone releasing peptide, in human volunteers.
Pharmaceutical research, 1999 Sep. human clinical.
October 29, 2024 Meeting of the Pharmacy Compounding Advisory Committee - FDA Briefing Document 4 - Ipamorelin
U.S. Food and Drug Administration, 2024-10-29. regulatory.
Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic Performance.
PubMed / Sports Medicine, 2026. review.
2026 Prohibited List: International Standard
World Anti-Doping Agency, 2025. official guidance.
The 2026 List of Prohibited Substances and Methods
World Anti-Doping Agency, 2026. regulatory.