The Definitive Peptide Research Reference Guide — Compound Review

Dosage Hub

GHRH Analogues Dosage Guide

Side-by-side dosing protocols for Sermorelin, CJC-1295 (with and without DAC), and Tesamorelin — injection timing, stacking with Ipamorelin, reconstitution, and cycle length.

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Research Disclaimer: This dosage information is for educational and research purposes only. With the exception of Tesamorelin (FDA-approved for HIV-associated lipodystrophy), GHRH analogues are not approved for general human use. Always consult a qualified healthcare professional before considering any peptide protocol.

GHRH analogues are synthetic peptides that mimic the action of endogenous growth hormone-releasing hormone (GHRH) at pituitary GHRH receptors. All members of this class — Sermorelin, CJC-1295, and Tesamorelin — share the same fundamental mechanism but differ in half-life, receptor binding affinity, and clinical application. This hub aggregates the dosing protocols for all three compounds in one reference.

Compound Dosage Reference

Sermorelin

GHRH analogue (29-aa fragment)

Half-life:~10–20 min
Standard dose:200–500 mcg
Frequency:1–2× daily
Best for:GH deficiency, anti-aging, physiological GH restoration
FDA status:Withdrawn 2008 (was approved 1997)
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CJC-1295 (No DAC)

GHRH analogue (Mod GRF 1-29)

Half-life:~30 min
Standard dose:100–200 mcg
Frequency:2–3× daily
Best for:GH optimization, stacking with Ipamorelin, body composition
FDA status:Not approved

CJC-1295 (With DAC)

GHRH analogue + albumin binder

Half-life:6–8 days
Standard dose:1–2 mg
Frequency:1–2× weekly
Best for:Convenience protocols, sustained GH elevation
FDA status:Not approved

Tesamorelin

GHRH analogue (full 44-aa + trans-3-hexenoic acid)

Half-life:~26 min
Standard dose:2 mg
Frequency:1× daily
Best for:Visceral fat reduction, FDA-approved lipodystrophy use
FDA status:FDA-approved (Egrifta) — HIV lipodystrophy

Side-by-Side Dosage Comparison

ParameterSermorelinCJC-1295 (No DAC)Tesamorelin
Standard dose200–500 mcg100–200 mcg2 mg
Frequency1–2× daily2–3× daily1× daily
RouteSubcutaneousSubcutaneousSubcutaneous
Half-life~10–20 min~30 min~26 min
GH release patternPulsatilePulsatilePulsatile
Typical cycle8–12 weeks8–12 weeksOngoing (FDA) / 3–6 mo (research)
Reconstitution (2 mg vial + 2 mL BAC)100 mcg = 0.10 mL100 mcg = 0.10 mL1 mg = 0.50 mL
Best stackGHRP-2 or GHRP-6IpamorelinIpamorelin (research)

Optimal Injection Timing Windows

All GHRH analogues share the same timing principles. GH release is suppressed by elevated insulin, so injections should be timed around fasted states or low-carbohydrate windows.

WindowTimingBenefitPriority
Fasted MorningUpon waking, before food or coffeeMaximizes GH pulse amplitude; fasted state prevents insulin suppression of GHHigh
Pre-Workout30–45 min before exerciseAmplifies exercise-induced GH release; synergistic with physical training stimulusHigh
Pre-Sleep30–60 min before sleepAmplifies natural nocturnal GH pulse; most important window for most protocolsHighest
Post-Workout30–60 min after trainingSupports recovery; some protocols use this window for tissue repair focusModerate

Universal Reconstitution Protocol

All GHRH analogues follow the same reconstitution process. The steps below apply to Sermorelin, CJC-1295 (both forms), and Tesamorelin.

  1. 1Wipe the vial stopper with an alcohol swab and allow to dry for 30 seconds.
  2. 2Draw 1–2 mL of bacteriostatic water (BAC water) into a syringe.
  3. 3Insert the needle into the vial and inject the water slowly along the inner wall — do not aim directly at the lyophilized powder.
  4. 4Gently swirl the vial until the powder fully dissolves. Do not shake — shaking can degrade the peptide.
  5. 5Store the reconstituted vial at 2–8°C (standard refrigerator). Use within 28–30 days.
  6. 6For injection: draw the required volume using a U-100 insulin syringe and inject subcutaneously into the abdomen, rotating sites.

Stacking GHRH Analogues with Ipamorelin

The most effective GH optimization protocols combine a GHRH analogue with a GHRP (growth hormone-releasing peptide). Ipamorelin is the preferred GHRP for stacking due to its selective profile — it produces clean GH pulses without elevating cortisol, prolactin, or appetite. The two classes act on complementary receptors (GHRHR and GHS-R1a), producing synergistic GH release.

StackGHRH DoseIpamorelin DoseFrequencyGoal
CJC-1295 + Ipamorelin100–200 mcg100–200 mcg2–3× dailyGH optimization, body composition
Sermorelin + Ipamorelin200–300 mcg100–200 mcg1–2× dailyAnti-aging, physiological GH
Tesamorelin + Ipamorelin2 mg100–200 mcg1× dailyVisceral fat, research protocol

Individual Dosage Guides

Frequently Asked Questions

What is the standard dosage for GHRH analogues?

Dosing varies by compound. Sermorelin is typically dosed at 200–500 mcg per injection, 1–2× daily. CJC-1295 without DAC (Mod GRF 1-29) is dosed at 100–200 mcg per injection, 2–3× daily. CJC-1295 with DAC is dosed at 1–2 mg once or twice weekly. Tesamorelin's FDA-approved dose is 2 mg once daily (subcutaneous). All GHRH analogues are most effective when injected on an empty stomach or before sleep.

Which GHRH analogue has the best dosing convenience?

CJC-1295 with DAC offers the most convenient dosing — once or twice weekly injections due to its 6–8 day half-life from albumin binding. Tesamorelin requires once-daily injections but has the advantage of FDA approval and clinical validation. Sermorelin and CJC-1295 without DAC require 2–3 daily injections for optimal pulsatile GH release, which more closely mimics the body's natural GHRH pattern.

Should GHRH analogues be stacked with a GHRP like Ipamorelin?

Yes — stacking a GHRH analogue with a GHRP (particularly Ipamorelin) is the most studied and effective approach for GH optimization. GHRH analogues prime the pituitary via GHRH receptors; Ipamorelin triggers GH release via GHS-R1a receptors. The dual-receptor mechanism produces synergistic GH pulses 2–10× greater than either peptide alone. CJC-1295 + Ipamorelin is the most widely used combination.

What is the best time to inject GHRH analogues?

The pre-sleep injection is the most important window for all GHRH analogues, as it amplifies the natural nocturnal GH pulse. Additional injection windows include fasted morning (maximizes GH pulse amplitude) and 30–45 minutes pre-workout (amplifies exercise-induced GH release). Avoid injecting within 2 hours of a carbohydrate-rich meal, as elevated insulin suppresses GH release.

How long should a GHRH analogue cycle last?

Sermorelin and CJC-1295 without DAC protocols typically run 8–12 weeks, followed by a 4-week break. Longer protocols of 3–6 months are used for body composition goals when stacked with Ipamorelin. Tesamorelin's FDA-approved protocol for HIV-associated lipodystrophy is continuous (ongoing), but research protocols typically cycle 3–6 months. Cycling prevents pituitary receptor desensitization.

How do you reconstitute GHRH analogue peptides?

All GHRH analogues follow the same reconstitution process: add 1–2 mL of bacteriostatic water to the lyophilized vial, injecting slowly along the side wall (not directly onto the powder). Gently swirl — do not shake. Store reconstituted peptide at 2–8°C and use within 28–30 days. For a 2 mg vial reconstituted with 2 mL, each 0.1 mL (10 units on a U-100 insulin syringe) equals 100 mcg.

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Medical Disclaimer: All content on this site is for educational and research purposes only. Research peptides are not FDA-approved for human use. Always consult a qualified healthcare professional before considering any peptide or supplement protocol. Nothing on this site constitutes medical advice, diagnosis, or treatment.