Peptides: Ipamorelin + CJC-1295 Stack Reference Card

Category: growth-hormone Updated: 2026-04-04

CJC-1295 combined with GHRP amplified IGF-1 response in humans beyond either alone (PMID 16368745). Synergy derives from simultaneous GHRH-R and GHSR stimulation.

Key Data Points
MeasureValueUnitNotes
Evidence GradeC/BgradeStack combination: Grade C — no direct human RCTs for this specific pair. Individual components: Grade B (human PK data for each)
Ipamorelin Dose200–300mcg/injectionStandard dose per injection; inject simultaneously with CJC-1295 no-DAC; 2–3× daily
CJC-1295 No-DAC Dose100–200mcg/injectionMod GRF 1-29 form only — NOT the DAC form; injected at same time as ipamorelin in separate syringe
Synergistic GH Amplification~3–4×vs either aloneExtrapolated from GHRH + GHRP dual-receptor synergy data; greatest GH pulse when both injected simultaneously (PMID 16368745)
Cycle Duration12weeks onStandard cycle; minimum 4 weeks off before repeating; receptor desensitization risk with continuous use
Optimal Injection WindowPre-sleep fastedtimingAligns with natural GH pulse ~60 min after sleep onset; must be fasted ≥2 hours; no food for 30–60 min post-injection
Receptor MechanismDual: GHRH-R + GHSRsynergy basisCJC-1295 no-DAC acts on GHRH-R; ipamorelin acts on GHSR; different receptors on same pituitary somatotroph cells — multiplicative effect

The ipamorelin + CJC-1295 no-DAC combination is the most widely used GH peptide stack in research and performance contexts. Its popularity derives from a combination of strong mechanistic rationale, acceptable individual safety profiles, and the selectivity advantages of ipamorelin (minimal cortisol/prolactin elevation) paired with the pulsatile GH amplification of CJC-1295 no-DAC (Mod GRF 1-29).

The synergy mechanism is straightforward: ipamorelin activates GHSR-1a (the ghrelin receptor) on pituitary somatotrophs, while CJC-1295 no-DAC simultaneously activates GHRH-R (the GHRH receptor) on the same cells. These are different receptors with different downstream signaling cascades, both converging on GH granule release — the combined signal produces a GH pulse approximately 3–4× greater than either compound alone (extrapolated from PMID 16368745; PMID 9861545).

No direct human RCT has studied this exact pair. The stack evidence is Grade C (extrapolated mechanistic), while individual components carry Grade B (human pharmacokinetic data).

Protocol Reference Card

ComponentDoseTimingRouteCycleNotes
Ipamorelin200–300mcg2–3× daily; pre-sleep preferredSubcut (abdomen/flank)12 weeks onInject simultaneously with CJC-1295 no-DAC; separate syringes
CJC-1295 no-DAC (Mod GRF 1-29)100–200mcgSame injection session as ipamorelinSubcut12 weeks onMUST be no-DAC form; do not substitute DAC form
Off-cycle break4 weeks minimumAllow axis recalibration; assess IGF-1 levels if monitoring bloods

Injection Timing Guide

Time of DayFood StatusRationalePractical Notes
Pre-sleep (optimal)Fasted ≥2 hours; no food 30–60 min post-injectionAligns with natural sleep-onset GH pulse; longest fasted window of dayMost effective injection; set alarm if needed to inject 20–30 min before sleep
Fasted morning8–12 hours fasted (overnight); no food for 30 min afterLow somatostatin from overnight fast; second-best windowInject on waking; wait 30–60 min before breakfast
Pre-workout fasted≥2 hours post-last-meal; pre-trainingExercise amplifies GH response; fasted state reduces somatostatinWorks well for morning trainers; less optimal for evening fed-state training
Post-workout fedWithin 1 hour of high-carb mealElevated insulin maximizes somatostatin — strongly blunts GH responseNot recommended; reduces effectiveness by 50–75%

Why the CJC-1295 No-DAC Form Is Essential

Using CJC-1295 with DAC instead of no-DAC fundamentally changes this protocol. The DAC form’s 6–8 day half-life creates continuous GHRH-R stimulation, blunting the pulsatile GH pattern. The no-DAC form has a ~30-minute half-life that clears between doses, preserving the 2–3× daily pulsatile pattern. The entire protocol design — injecting at specific times in a fasted state — is built around pulsatile GH release. Using the DAC form removes this logic and transforms the protocol into a continuous GH elevation approach with different pharmacological effects.

Cycling and Receptor Desensitization

The 12-weeks-on / 4-weeks-off cycle structure is designed to prevent GHSR and GHRH-R downregulation. Continuous agonist exposure leads to receptor internalization and desensitization. After 12 weeks of twice or thrice-daily dosing, GH pulse amplitude typically begins to attenuate. The 4-week off-cycle allows receptor recycling and axis normalization before the next cycle.

JurisdictionStatusScheduleNotes
USABoth research chemicalsNeither scheduledBoth WADA prohibited (S2); not FDA-approved
UKNeither scheduledNoneLegal to possess; both WADA prohibited under UKAD rules
AustraliaBoth prescription restrictedBoth Schedule 4 (TGA)Both ASADA prohibited for competitive athletes
CanadaBoth gray marketNo scheduleNo approved DINs; both WADA prohibited
EUBoth generally unscheduledVaries by countryNo EMA approval; both WADA prohibited
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Frequently Asked Questions

Why must ipamorelin and CJC-1295 no-DAC be injected simultaneously?

The synergistic GH pulse requires both receptor types (GHRH-R and GHSR) to be activated simultaneously. Pituitary somatotrophs receive both signals at the same time and produce a pulse approximately 3–4× larger than either stimulus alone. Injecting them separately — even 30 minutes apart — reduces the synergistic overlap and produces two smaller pulses rather than one large combined pulse.

Does this stack suppress endogenous GH production long-term?

GH peptide stacks amplify natural GH pulses rather than replacing endogenous GH. Unlike exogenous recombinant GH, GHRPs and GHRH analogues do not directly suppress pituitary GH production. However, the off-cycle period (4 weeks minimum) is still recommended to prevent receptor desensitization and allow the hypothalamic-pituitary axis to recalibrate. No human studies have characterized long-term suppression effects from peptide-only protocols.

What is the evidence grade for the combined ipamorelin + CJC-1295 stack?

The specific combination of ipamorelin and CJC-1295 no-DAC has not been studied directly in human RCTs — it is Grade C as a stack. Individual components have Grade B evidence from human pharmacokinetic studies. The synergy rationale is well-founded mechanistically (PMID 9861545; 16368745) but has not been confirmed in a controlled body composition trial.

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