library.onepin.app/cjc-1295-no-dac-ghrp-6-blend Peptide Education Library
Education only, not medical advice 21+ Every dose is an example to finalize with a licensed provider
Growth Hormone Growth Hormone Secretagogue BlendNot FDA-approved · investigational

CJC-1295 no DAC / GHRP-6 Blend

CJC + GHRP-6

100mcg CJC + 100mcg GHRP-6 per injection – ~200 mcg total (100/100) SubQ 2-3x daily
GHRH + GHRP CombinationStrong appetite-stimulating GH blend29-Amino Acid Analog + Synthetic Hexapeptide

CJC-1295 no DAC / GHRP-6 Blend is a pre-mixed growth hormone secretagogue combination that pairs Modified GRF(1-29) with the original and most appetite-stimulating GHRP. This blend produces powerful pulsatile GH release through dual-receptor activation while delivering the strongest hunger drive of any GH peptide stack. GHRP-6 was the first synthetic ghrelin mimetic developed and remains the go-to GHRP for users who need or want significant appetite stimulation alongside GH optimization.

Quick Start
Route
Subcutaneous (SubQ) injection
Start low
100mcg CJC + 100mcg GHRP-6… SubQ
Frequency
2-3x daily
Timing
Fasted. Minimum 2 hours empty stomach. No eating for 30 min post-injection. Use the hunger window strategically for your largest meal.

Starting dose. 100mcg CJC + 100mcg GHRP-6 per injection

Start here. Every protocol below is ordered lowest-first. Begin at the smallest effective dose, hold about a week to assess tolerance, and step up only if needed.

Tiered Protocols · lowest first
Conservative start
100mcg CJC + 100mcg GHRP-6 per injection · Subcutaneous (SubQ) injection · 2-3x daily
conservative starter
100mcg CJC + 100mcg GHRP-6 per injection
2-3x daily
Standard
Mass / Appetite
~200 mcg total (100/100) · SubQ · 2x Daily
anecdotal · community
GHRP-6 drives intense ghrelin-mediated hunger ~20 min post-dose; favored for bulking.
~200 mcg total (100/100)
2x Daily
Reconstitution CalculatorU-100
050100u
Draw to
units
01

How it works

This blend works through dual-receptor stimulation of the GH axis with pronounced ghrelin-mediated appetite effects:

CJC-1295 no DAC (Mod GRF 1-29)

Binds GHRH receptors on pituitary somatotrophs, activating the cAMP/PKA signaling cascade to prime and release stored GH granules. The four amino acid substitutions protect against DPP-IV degradation, extending the half-life to approximately 30 minutes. Produces acute GH pulses preserving natural pulsatile patterns.

GHRP-6

Binds GHS-R1a (ghrelin receptor) on the pituitary with strong efficacy, triggering GH release through the PLC/IP3/PKC pathway. GHRP-6 has the strongest orexigenic effect of any GHRP because it activates hypothalamic appetite centers more potently than GHRP-2 or Ipamorelin. It also suppresses somatostatin, removing the natural brake on GH secretion. GHRP-6 elevates cortisol and prolactin in a dose-dependent manner - more than Ipamorelin, less than Hexarelin.

Synergistic Amplification

The simultaneous GHRH signal (CJC) and GHRP signal (GHRP-6) converge through independent intracellular pathways, producing GH pulses 3-5x greater than either peptide alone. This mimics the body's natural dual-signal GH regulation system.

Appetite Mechanism

GHRP-6 activates neuropeptide Y (NPY) and agouti-related peptide (AgRP) neurons in the arcuate nucleus of the hypothalamus, triggering strong hunger signaling within 15-20 minutes of injection. This is the same pathway activated by endogenous ghrelin before meals.

02

What to expect

Early
Days 1–7

Days 1-7: Strong appetite stimulation is the first and most obvious effect, peaking 15-20 minutes post-injection. Use this hunger window to time your largest meals. Improved sleep quality with deeper slow-wave sleep, especially with bedtime dosing. Possible mild water retention. Transient flushing or tingling post-injection is normal.

Mid
Weeks 2–4

Weeks 2-6: Body composition changes visible with adequate caloric intake. Muscle fullness and recovery improving. Skin quality starting to improve. Appetite effect becomes predictable and can be strategically timed around training and meals. Fat distribution may shift as GH levels optimize.

Later
Weeks 4–12

Weeks 6-12: Full body recomposition effects when paired with training and nutrition. Lean mass gains consolidated. Skin, hair, and connective tissue improvements visible. Consider cycling off after 8-12 weeks with a 4-week break to maintain pituitary sensitivity and prevent GHS-R1a desensitization.

03

Evidence

HumanStrong
AnimalPresent
In-vitroStrong

Claims we could not support

No abstract we checked supports these for this molecule at this route. That is not the same as saying they are false — it marks where the evidence is missing.

Dose/route: 100 mcg CJC + 100 mcg GHRP-6 SubQ 2-3 times daily while fasted. No checked abstract administered this exact fixed combination, ratio, SubQ dose, or frequency in humans.

Mechanism and claimed 3-5× GH-pulse synergy for the exact blend. GHRP-6 or DAC-CJC-1295 component evidence cannot establish the mechanism magnitude, formulation, or pharmacodynamics of this exact no-DAC fixed blend.

Primary safety concern, including appetite, cortisol, and prolactin effects for the blend. No checked human abstract evaluated safety of the exact fixed blend at the displayed regimen; component-only safety was not transferred.

04

The honest take

Strongest appetite stimulation of any GH peptide blend

Supported

Well-supported by human comparative data. GHRP-6 consistently produces the most intense hunger response among GHRPs, peaking at 15-20 minutes post-injection. This is due to stronger hypothalamic NPY/AgRP activation compared to GHRP-2 or Ipamorelin.

3-5x synergistic GH amplification from dual-receptor stimulation

Supported by GHRH + GHRP co-administration studies. The synergistic effect is well-established in the literature, though exact magnitude varies by individual and dose.

Strategic meal timing using post-injection hunger window

Practically validated. The 15-20 minute onset and 30-60 minute duration of appetite stimulation is consistent across users, making it predictable enough for meal timing strategies.

05

Interactions & stacking

Two different questions: what is documented about running these together, and what is documented about drawing them into the same syringe. A good pharmacological partner can still have to be pinned separately.

Documented together

AOD-9604No interaction. GH fragment peptide works through different pathway. Safe in same syringe.
GHK-CuCompatible for stacking. Draw GHK-Cu LAST due to copper. GH elevation enhances collagen remodeling.
MOTS-cMitochondrial peptide with independent mechanism. Safe in same syringe.
SelankNo reactive residue conflicts. Safe in same syringe.

Keep separate

CJC-1295 with DACDAC version provides continuous GH elevation that disrupts pulsatile signaling. Do not combine sustained and pulsatile GHRH analogs.
Somatostatin analogs (Octreotide)Directly antagonizes GH release. Completely negates the purpose of this blend.
High-dose insulinElevated insulin blunts GH response. Fasted state is required for optimal GH release from this blend.
NAD+Acidic pH of NAD+ can denature peptides. Different route anyway (NAD+ is typically IM or IV).

Check any specific pair in the Stack & Interaction Checker, which answers both questions separately. Absence of a documented conflict is not evidence of safety.

06

Side effects & safety

Commonly reported

  • Strong appetite increase 15-20 min post-injection lasting 30-60 min
  • Transient flushing or warmth post-injection (resolves in minutes)
  • Mild tingling or head rush immediately after injection
  • Mild water retention in first 1-2 weeks
  • Vivid dreams and improved sleep (desired effect)

Less common & notes

  • At higher GHRP-6 doses (above 200mcg), cortisol and prolactin elevation becomes more significant.
  • This can manifest as mild anxiety, irritability, or lethargy post-injection.
  • GHRP-6 has the strongest appetite effect of any GHRP - some users find the hunger unmanageable if not strategically planned.
  • Occasional stomach gurgling or GI discomfort from the ghrelin activation.
  • Keep individual GHRP-6 doses at or below 200mcg to balance GH output against hormonal side effects.
  • Both components have reasonable safety data, but long-term human combination studies are limited.
07

Pharmacokinetics

Illustrative plasma concentration · 17 h
Half-life

CJC-1295 no DAC: ~30 min; GHRP-6: ~20 min. Combined GH pulse duration: 1.5-2 hours.

Peak · Tmax

CJC: 15-30 min; GHRP-6: 15-20 min. Peak synergistic GH release at ~20-30 min post-injection.

Elimination

Both components cleared within 2-3 hours. GH pulse elevation returns to baseline by 3-4 hours.

Bioavailability

SubQ: ~95-100% for both components. Oral: not viable (peptide degradation in GI tract).

Duration of action

GH pulse lasts 1.5-2 hours. Downstream IGF-1 elevation persists 12-20 hours. Appetite effect from GHRP-6 lasts 30-60 minutes post-injection, peaking at 15-20 minutes.

Clearance

Enzymatic degradation by peptidases. CJC modifications provide DPP-IV resistance. GHRP-6 cleared primarily by renal and hepatic peptidases.

Storage. Store lyophilized vial at room temperature or refrigerated. After reconstitution with bacteriostatic water, store refrigerated at 2-8 degrees C. Use within 28-30 days of reconstitution. Do not freeze after reconstitution. Protect from prolonged light exposure. Discard if solution becomes cloudy or contains particulate matter.

08

Regulatory status

Not FDA-approved as a combination product. Available through compounding pharmacies with prescription. CJC-1295 no DAC (Mod GRF 1-29) has published human pharmacokinetic data. GHRP-6 has been studied in multiple human clinical trials for GH release and diagnostic purposes. Pre-mixed blends are a compounding pharmacy product. Classified as research peptides in most jurisdictions. All use is experimental and off-label.

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The guide & community

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