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For research, development and manufacturing use only. Not for human or veterinary use.

Growth Hormone & IGF · Source-reviewed dossier

CJC-1295 (without DAC) + Ipamorelin Blend

Source-Reviewed Research Dossier

This catalog item is a two-component research blend. It pairs a short-acting GHRH analogue that acts at the pituitary with an ipamorelin-type molecule that acts through the ghrelin receptor. Researchers study these two kinds of molecule because they represent separate control points on growth-hormone signalling. The human evidence for ipamorelin is a trial in hospitalized bowel-surgery patients who received it intravenously; the main outcome was not significantly better than placebo. The CJC-related evidence is analytical detection in seized powders, not a health effect. No controlled study of this exact mixture was identified, so its stability and combined behaviour are uncharacterized. For research use only.

Research use only Lot documents on request
CJC-1295 (without DAC) + Ipamorelin Blend research product family with 1 catalog variants
AI-generated packaging mockup for catalog navigation. It is not a photograph of an actual supplied lot; container, label and presentation may vary.

Product family

Compound overview

Shared values below are consolidated from the current catalog record. They are not independent verification or lot results; request the applicable product specification and ask which lot records are available before ordering.

Product identity

Product type
Multi-component research blend
Catalog family
CJC-1295 (without DAC) + Ipamorelin Blend
Research category
Growth Hormone & IGF
Identity boundary
No single CAS, formula, sequence or molecular weight applies to the two-component mixture.
Evidence status
No controlled trial of the exact blend; component evidence only
Intended use
Research, development and manufacturing use only

Literature reference parameters

Compound or material class
Modified GRF(1-29) / ipamorelin two-component blendCatalog-family identity
Evidence scope
No controlled trial of the exact blend; component evidence onlyDo not generalize beyond the cited model
Source review
Primary or authoritative records linked belowChecked 2026-09-01

Identity safeguard Reference identifiers above describe the literature compound record. Confirm the supplied form, formula, molecular weight, purity and storage conditions against the applicable product specification and any available lot records.

Mechanism of action

How CJC-1295 (without DAC) + Ipamorelin Blend is studied

A target-to-pathway view grounded in the linked research records.

Two control points for growth-hormone release

Growth-hormone release has more than one input. The GHRH analogue acts at the GHRH receptor; an ipamorelin-type molecule acts at the ghrelin receptor. Researchers combine different receptor inputs to ask whether one changes the other. The two act at different places, but no supplied experiment tested them together, so combined behaviour in this blend is unknown.

Why a short-acting GHRH analogue

GHRH is the main direct signal to the pituitary, a small gland near the brain. A short-acting analogue is studied when a brief pulse rather than a long signal is wanted, because pulse timing can affect downstream hormone patterns. Analytical records describe how modified GHRF-type material was identified in seized powders; that supports identity testing, not effects. A research analyte only.

Ipamorelin and ghrelin receptor

Ipamorelin is studied as a selective ghrelin-receptor agonist, a separate input from GHRH. It was also tested outside hormones: a randomized phase 2 trial gave intravenous ipamorelin to bowel-resection patients with postoperative ileus. It was tolerated, but the key meal-tolerance comparison did not separate from placebo. Small size and mixed patients were limitations. That trial used intravenous drug, not this blend.

What the mixture does and does not add

A catalog blend is a supplied physical mixture, not a characterized formulation. No controlled publication was identified for this exact combination. Co-stability, ratio behaviour and possible interaction between the two components are not established by the supplied references. Component findings belong to their own material, model and route. Lot identity and purity depend on product-specific analytical documents, not blend-level evidence.

Reported research findings

What published studies report about CJC-1295 (without DAC) + Ipamorelin Blend

Reported outcomes are paired with their experimental model and evidence boundary.

Phase 2 component trial

Ipamorelin missed its primary clinical comparison

In a 117-patient postoperative-ileus study, the 25.3 versus 32.6 hour median comparison had p=0.15.

The intravenous protocol does not test this blend or another route.

Read the primary study
Analytical study

Modified GHRF-related material has been identified in seized products

Mass-spectrometric work characterized glycine-modified GH secretagogues including modified GRF-related material.

Analytical detection supports identity controls, not safety or efficacy.

Read the primary study
Translation boundary: findings are limited to the evidence level stated on each card. Experimental protocol quantities are research details, not usage instructions.

Catalog options

Variant specifications

Pack-level catalog data; lot-level controls remain document-specific.

Catalog no.CP10
Pack size10 mg × 10 vials
Current variant
Specification & documents for CP10

Product specification

Multi-component research blend · 10 mg/vial catalog presentation · 10-vial pack · component identity and ratio controlled by product specification.

Lot documentation

Document availability and scope must be confirmed for this variant and lot in the written quotation. A catalog description is not a lot-specific test result.

Quality system

Quality documentation

A listed document is not proof of availability for this lot. Ask the team to confirm the current COA status and the scope of any other records before ordering.

Lot-specific Certificate of AnalysisAvailability and scope must be confirmed for the selected catalog variant and lot
COA availability unconfirmed Ask about availability
Product Specification SheetAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request
Analytical Method SummaryAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request

Analytical interpretation

Interpret the documents, not just the headline number.

Use the source-reviewed guide to separate chromatographic area purity, quantitative assay, LC-MS identity, composition and stability evidence before comparing variants or requesting a lot record.

Open the Quality & Documentation Hub

HPLC area ≠ assayA dominant peak does not establish target mass fraction.

Intact mass ≠ full sequenceIdentity strength depends on resolution and orthogonal evidence.

Counterions affect contentWater, salt form and solvents change the as-is composition.

Storage needs a data basisShipping practice is not the same as stability evidence.

Evidence map

Research context

Published studies and regulatory records, not customer testimonials or usage guidance.

Phase 2 component trial

Ipamorelin missed its primary clinical comparison

The intravenous protocol does not test this blend or another route.

View primary record
Analytical study

Modified GHRF-related material has been identified in seized products

Analytical detection supports identity controls, not safety or efficacy.

View primary record
Evidence boundary: each card states its evidence type. Human trials and regulatory records describe the studied or regulated intervention; preclinical records remain model-specific. None verifies the identity, quality, safety or efficacy of this catalog lot or provides usage instructions.

Literature basis

Curated references

Third-party publications selected for direct relevance.

  1. 01

    Randomized ipamorelin study after bowel resection

    Beck DE, et al. International Journal of Colorectal Disease. 2014. PMID 25331030.

    Phase 2
  2. 02 Analytical study

Research FAQ

CJC-1295 (without DAC) + Ipamorelin Blend questions

Concise answers for researchers comparing identity, evidence and catalog variants.

What effects are studied for CJC-1295 (without DAC) + Ipamorelin Blend?

The strongest human record is the ipamorelin phase 2 trial in bowel-resection patients with postoperative ileus. Intravenous ipamorelin was tolerated, but the primary meal-tolerance comparison did not differ significantly from placebo. The CJC-related source identified modified GHRF-type material in seized powders. Neither source documents an effect of this two-component blend, and no controlled study of the exact mixture was found.

How should the CJC-1295 (without DAC) + Ipamorelin Blend research findings be understood?

A catalog blend is a supplied physical mixture, not a characterized formulation. No controlled publication was identified for this exact combination. Co-stability, ratio behaviour and possible interaction between the two components are not established by the supplied references. Component findings belong to their own material, model and route. Lot identity and purity depend on product-specific analytical documents, not blend-level evidence.

What evidence is available for CJC-1295 (without DAC) + Ipamorelin Blend?

Component-level human and analytical records exist, but direct evidence for this combined formulation is absent.

Does the cited research validate this catalog material?

No. The cited records describe their own intervention, formulation, model and controls. They do not verify the identity, purity, sterility, safety or efficacy of a catalog lot.

Which quality documents can be requested?

A lot-specific COA, product specification sheet and analytical method summary can be requested where applicable.

How should CJC-1295 (without DAC) + Ipamorelin Blend be stored?

Store at -20 °C, protected from light and moisture. After reconstitution, aliquot and avoid repeated freeze-thaw cycles. Confirm the applicable storage statement on the product-specific specification and lot documentation.

Knowledge tools

Continue with structured evidence

Move from this dossier into canonical evidence maps, verified status records, analytical interpretation and laboratory calculations.

Internal technical source review

Claims were checked against the linked primary publication, regulatory label or authoritative compound record. Published findings stay attached to their study model, formulation and route. Catalog identity and lot quality remain controlled by the applicable specification and lot-specific documents.

Editorial status: NHD evidence editorial workflow · 2026-09-01 · Not independent medical review · Review policy

Technical procurement

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Selected: CP10 · 10 mg × 10 vials