Educational research reference · Not medical advice · Compounds discussed are research materials, not approved drugs
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CJC-1295 / Ipamorelin Blend Protocol: Dosing, Reconstitution & Research (2026)

A research reference for the co-formulated CJC-1295 (no-DAC) + Ipamorelin blend — a GHRH analog paired with a selective ghrelin-receptor agonist, dosed as a single product with bedtime, empty-stomach timing.

CJC-1295 / Ipamorelin Quick Start

This is a single co-formulated blend of two growth-hormone secretagogues that act on different receptors. CJC-1295 no-DAC (also sold as Mod GRF 1-29) is a stabilised GHRH fragment; Ipamorelin is a selective agonist at the ghrelin/GHS receptor. Pairing a GHRH analog with a GHS-receptor agonist is the standard secretagogue research approach because the two amplify each other rather than duplicating one pathway.

Quick reference Combined blend · preclinical
Type
Co-formulated 2-peptide blend
Formats
Vial (SubQ)
Action
GHRH analog + GHS-R agonist
Total content
10 mg per vial
Timing
Bedtime, empty stomach

This guide is an educational research reference. It does not diagnose, treat, or prescribe, and is not medical advice. Consult a licensed clinician before considering any compound.

CJC-1295 / Ipamorelin Composition

The product listing specifies 10 mg total per vial but does not publish the split between the two components. A 1:1 division is the common convention for this pairing; confirm the actual ratio against the batch Certificate of Analysis before treating any per-component figure as exact.

ComponentRoleReceptorHalf-life character
CJC-1295 (no-DAC)GHRH analogGHRH receptorShort — ~30 min, pulse-preserving
IpamorelinGhrelin mimeticGHS-R1aShort — ~2 h, selective

CJC-1295 / Ipamorelin Dosing Protocol

The blend is dosed as one product. Ranges below are community-derived research-planning references, not personal dosing recommendations. Because both components are short-acting and the goal in the literature is to preserve the body's natural pulsatile release, dosing is timed to a natural GH pulse — bedtime, on an empty stomach.

Injection — Subcutaneous

Reconstituted 10 mg vial, subcutaneous. Doses are stated by mass — the syringe-unit equivalent depends on your reconstitution volume, worked out below.
BandPer dose (blend)Frequency
Low100 mcgOnce nightly
Standard200 mcgOnce nightly
High300 mcgOnce nightly
10 mg + 2 mL BAC → 5,000 mcg/mL · 100 mcg = 2 units · ~50 doses per vial at 200 mcg
Timing matters more here than with most compounds. Both components are short-acting, and food — carbohydrate and fat especially — blunts the GH response. Published secretagogue protocols consistently use a fasted window of at least two hours before and roughly 30 minutes after.

Cycle guidelines

ApproachDurationReview pointBest for
Standard8–12 weeksWeek 8General research planning
Extended12–16 weeksWeek 12Slower body-composition endpoints

Off periods of 4 weeks are common in research planning. There is no published human cycling RCT for this blend.

CJC-1295 / Ipamorelin Reconstitution Guide

The blend ships as a lyophilized powder. The bacteriostatic water volume sets the concentration and the draw size; 2 mL is the common convention for a 10 mg vial.

Injection

BACConc.200 mcg
2 mL5,000 mcg/mL0.04 mL · 4 u
3 mL3,333 mcg/mL0.06 mL · 6 u

Units are U-100 insulin-syringe units (100 u = 1.0 mL).

Per-component figures

Because the listing does not publish the split, the tables above are stated as blend totals. If the COA confirms a 1:1 division, a 200 mcg dose is 100 mcg of each component.

Reconstitution steps

  1. Inspect the vial. Confirm the label, expected milligram amount, and that the powder looks dry and intact.
  2. Wipe the stoppers. Use an alcohol swab on both the bacteriostatic water and peptide vial stoppers.
  3. Draw the chosen volume. 2 mL into the vial — this is the number that sets every concentration figure above.
  4. Inject down the wall. Release the water slowly down the inside wall, not directly onto the powder.
  5. Swirl, do not shake. Roll gently until dissolved. Shaking foams and can damage the peptide.
  6. Verify clarity. Solution should be clear and colorless. Discard if cloudy or particulate.
  7. Label and refrigerate. Note the date and volume added on the vial, then store at 2–8 °C. Do not freeze the reconstituted solution.

See the bacteriostatic water guide for diluent handling, or the reconstitution calculator to work any other volume.

Why These Two Together

GHRH analogs and ghrelin mimetics drive growth-hormone release through separate receptors, and combining them produces a larger release than either alone in published secretagogue work. Ipamorelin is favoured over older GHS compounds because it is selective — it does not meaningfully raise cortisol or prolactin, which was the limitation of earlier molecules in the class.

CJC-1295 no-DAC

Stimulates the GHRH receptor on the pituitary; the no-DAC form keeps the pulse short.

Ipamorelin

Selective GHS-R1a agonist; amplifies the pulse without the cortisol/prolactin rise of older GHS drugs.

Pulsatility

Both are short-acting by design — the aim is to mimic a natural pulse, not create a sustained elevation.

Open question

Long-term human data for the combination is absent; the rationale is component-level and mechanistic.

Who Should Avoid CJC-1295 / Ipamorelin

Growth-hormone-axis compounds act upstream of a broad hormonal cascade, so eligibility is a clinical question rather than a dosing one.

Active or prior cancer

Raising GH and IGF-1 is a theoretical proliferation concern; consistently flagged as a contraindication.

Diabetes or insulin resistance

GH is counter-regulatory to insulin and can worsen glycaemic control.

Pregnancy & lactation

No human safety data.

Tested athletes

GH secretagogues are prohibited in sport under WADA S2; use is an anti-doping rule violation.

CJC-1295 / Ipamorelin Side Effects & Safety

Injection-site reactions

Redness or itching at the site is the most commonly reported short-term effect; rotate sites.

Water retention & tingling

Mild oedema, joint aches or carpal-tunnel-type tingling are classic GH-axis effects and are dose-related.

Glycaemic effects

GH opposes insulin; glucose handling can shift, which matters most for anyone already insulin-resistant.

Quality-control risk

A blend cannot be visually distinguished from a single peptide — verify identity and per-component purity against a COA.

CJC-1295 / Ipamorelin Evidence Context

Ipamorelin pharmacology

Characterised as a selective GHS-R agonist that raises GH without the cortisol and prolactin effects of earlier compounds.

GHRH analog literature

CJC-1295 and Mod GRF 1-29 have published pharmacokinetic work showing GH and IGF-1 elevation.

Combination data

Human trial data for this specific co-formulation is absent; the rationale is component-level.

Open question

Whether pulsatile secretagogue elevation produces the outcomes attributed to it has not been established in controlled trials.

Storage & Handling

StateStorageNotes
Lyophilized (powder)−20 °C, protected from lightMore stable than reconstituted solution.
Reconstituted (liquid)2–8 °C−20 °C for longer storage per the listing.
AppearanceClear, colorlessDiscard cloudy or particulate solutions.

Blend vs Sermorelin

FeatureCJC-1295 / IpamorelinSermorelin
CompositionGHRH analog + ghrelin mimeticGHRH analog alone
ReceptorsGHRH-R and GHS-R1aGHRH-R only
RationaleTwo pathways amplify the pulseSingle-pathway, closest to native GHRH
PageThis pageSermorelin

Frequently Asked Questions

Is this two separate vials?

No. It is a single co-formulated blend — one 10 mg vial containing both peptides, dosed as one product.

How much of each component is in a dose?

The listing publishes only the 10 mg total, not the split. A 1:1 division is the common convention, which would make a 200 mcg dose 100 mcg of each — but confirm against the batch COA rather than assuming.

Why dose at bedtime?

Both components are short-acting and the approach in the literature is to amplify a natural GH pulse. The largest natural pulse occurs shortly after sleep onset, and food blunts the response.

How is it reconstituted?

10 mg in 2 mL of bacteriostatic water gives 5,000 mcg/mL, so a 200 mcg dose is 4 units on a U-100 syringe.

Is it banned in sport?

Yes. Growth-hormone secretagogues fall under WADA category S2 and are prohibited at all times.

Is this page medical advice?

No. It is an educational research reference and does not diagnose, treat, or prescribe. Consult a licensed clinician before considering any compound.

CJC-1295 / Ipamorelin Formats & Sourcing

The blend is supplied as a lyophilized powder in a single 10 mg vial. There is no pre-reconstituted pen or spray format for this product. Batch-specific Certificates of Analysis are issued per lot and are the place to confirm the component split.

FormatSupplied as
Vial10 mg total lyophilized blend

Strengths are listed as sold; confirm against the product page and the batch COA before calculating anything.

Reference material for this protocol, with batch COA:

View CJC-1295 / Ipamorelin on Spyro Peptides →
Purity ≥98% HPLC Batch COA available Research use only

References

  1. Raun K, et al. Ipamorelin, the first selective growth hormone secretagogue. Eur J Endocrinol (1998).
  2. Teichman SL, et al. Prolonged stimulation of GH and IGF-I secretion by CJC-1295. J Clin Endocrinol Metab (2006).
  3. Sinha DK, et al. Beyond the androgen receptor: the role of growth hormone secretagogues. Transl Androl Urol (2020).
  4. World Anti-Doping Agency. Prohibited List 2025 — S2 peptide hormones and growth factors.