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ID: CJC-1295 STATUS: ACTIVE

CJC-1295

Research Only

Also known as: DAC:GRF, Modified GRF 1-29, Tetrasubstituted GRF

A synthetic analog of growth hormone-releasing hormone (GHRH) with extended half-life. Limited clinical development; not approved for any indication.

Hormonal Moderate Evidence 14 Sources

Research Statistics

Total Sources
14
Human Studies
4
Preclinical
2
Evidence Rating Moderate Evidence
Research Depth 3/5
Global Coverage 2/5
Mechanism Plausibility 3/5
Overall Score
3 /5

GHRH analog with Phase 1 human data; mechanism well-understood via GHRH receptor.

Last reviewed February 2026 How we rate →
~
Evidence Level
moderate
Not approved for human use by any regulatory agency
Limited human clinical trial data
Consult a healthcare provider before use
Not FDA Approved WADA Prohibited

Research Dossier

01 / 7

Overview

What is CJC-1295 and what does the research say?

Identity
Also Known As
DAC:GRF • Modified GRF 1-29 • Tetrasubstituted GRF
Type
Tetrasubstituted GHRH Analog
Length
29 amino acids
Weight
3,367.97 Da
Sequence
YADAIFTNSYRKVLGQLSARKLLQDILSR
Molecular Structure
Y
D-A
D
A
I
F
T
Q
S
Y
R
K
V
L
A
Q
L
S
A
R
K
L
L
Q
D
I
L
S
R
Hydrophobic
Polar
Positive
Negative

Mechanism of Action

CJC-1295 is a modified version of GHRH (growth hormone-releasing hormone) engineered for extended duration. The modifications confer resistance to enzymatic degradation and enable prolonged receptor activation.

How It Works (Simplified)

CJC-1295 stimulates growth hormone release through four key mechanisms:

1
DPP-IV Resistance

Four amino acid substitutions at positions 2, 8, 15, and 27 prevent degradation by dipeptidyl peptidase IV, extending half-life from minutes to hours.

2
Albumin Binding (DAC)

The DAC version contains maleimidoproprionic acid that covalently binds to serum albumin, extending half-life to 6-8 days.

3
GHRH-R Activation

Binds to GHRH receptors on pituitary somatotrophs, activating Gαs-adenylyl cyclase-cAMP-PKA signaling cascade.

4
GH/IGF-1 Elevation

Sustained receptor activation produces prolonged GH secretion (2-10 fold for 6+ days) and IGF-1 elevation (9-11 days after single dose).

Scientific Pathways

GHRH-R Signaling Pathway (GH Release)

CJC-1295 → GHRH-R binding → Gαs activation → Adenylyl cyclase

                                          ↑ cAMP → PKA activation

                                          GH synthesis and secretion

DAC Albumin Conjugation (Extended Half-Life)

CJC-1295 DAC → MPA group → Covalent binding to albumin Cys34

                          Half-life extended to ~6-8 days

                          Sustained GH/IGF-1 elevation

Key Research: Teichman SL et al. (2006) demonstrated 2-10 fold GH elevation for 6+ days and IGF-1 elevation for 9-11 days in Phase 1/2 trials. PMID:16352683

Important Limitations

  • Clinical development discontinued in 2006 after participant death (deemed unrelated to drug - pre-existing coronary disease)
  • No approved indications in any country
  • WADA prohibited substance
  • Sustained vs pulsatile GH elevation may have different safety profiles
  • Long-term effects of chronic IGF-1 elevation unknown
  • Limited human clinical data due to early termination of development program

Evidence-Chained Benefits

Evidence-Chained Benefits

Research findings linked to mechanisms and clinical outcomes

Mechanism GHRH receptor agonism with extended half-life via albumin binding (DAC)
Established 6 direct studies
Benefit shown to produce sustained elevation of growth hormone and IGF-1
Evidence Level
Low
2 Human
2 Animal
1 In Vitro
Mechanism Tetrasubstitution conferring DPP-IV resistance at positions 2, 8, 15, 27
Established 4 direct studies
Benefit shown to extend half-life from minutes to 5-8 days
Evidence Level
Moderate
2 Human
2 Animal
1 In Vitro
Mechanism JAK-STAT and cAMP-PKA pathway activation in somatotrophs
Supported 3 direct studies
Benefit appears to stimulate pituitary GH synthesis and release
Evidence Level
Low
1 Human
2 Animal
2 In Vitro
Mechanism Confidence
Established
Supported
Emerging
Evidence Level
High
Moderate
Low
Very Low

What to Expect

Timeline based on observations from published studies. Individual responses may vary.

Based on Phase 1 data: Single injection of CJC-1295 DAC produced IGF-1 elevation within 24-48 hours. GH pulsatility patterns may begin to change. Steady-state levels not yet achieved.

Phase 1 studies showed sustained IGF-1 elevation lasting 9-11 days after single dose. With repeated dosing (weekly or twice-weekly), approaching steady-state levels. GH response patterns established.

Steady-state GH/IGF-1 elevations achieved with regular administration. In growth-deficient mouse models, normalization of growth occurred over this timeframe. Body composition changes may begin.

Week 8+

Limited long-term human data available. Animal studies suggest maintained efficacy. Clinical development was discontinued, so extended human timeline data is lacking.

Research-Based Observations

This timeline reflects observations from published clinical and preclinical studies. Individual responses may vary significantly. This is not a guarantee of effects or a dosing schedule. Consult qualified healthcare providers for personalized guidance.

Quality Checklist

Visual indicators to help evaluate CJC-1295 product quality

Good Signs (7 indicators)
White to off-white lyophilized powder
Dissolves completely in bacteriostatic water
Clear, colorless solution after reconstitution
Certificate of analysis showing >98% purity
HPLC verification of identity and purity
Proper vacuum seal and vial integrity
Labeled as CJC-1295 with or without DAC (know which variant)
Warning Signs (5 indicators)
Slightly off-white or cream colored powder
Slower dissolution than expected
COA without third-party verification
Unclear whether product contains DAC modification
Purity between 95-98%
Bad Signs (7 indicators)
Yellow or brown discoloration
Particles or cloudiness after reconstitution
Gel-like consistency or incomplete dissolution
No COA or certificate appears fabricated
Mislabeled DAC vs non-DAC variant
Unusual odor
Compromised vial seal
Positive quality indicator
Requires evaluation
Potential quality issue

For Research Evaluation Only

These quality indicators are general guidelines based on typical peptide characteristics. Professional laboratory testing (HPLC, mass spectrometry) provides definitive quality verification. This checklist is for initial visual evaluation only.

Peptide Interactions

Known and theoretical interactions when combining CJC-1295 with other peptides. Based on published research and mechanistic considerations.

Synergistic
Compatible
Caution
Avoid

Commonly combined in research. CJC-1295 (GHRH analog) stimulates GH release via GHRH receptor while ipamorelin acts on ghrelin receptor. Different mechanisms may produce additive GH release.

GHRH + GHRP combination produces greater GH release than either alone. CJC-1295 amplifies GH pulse while GHRP-6 initiates it via ghrelin receptor.

Similar synergistic mechanism as GHRP-6. GHRH and GHRP act through complementary pathways to enhance GH secretion.

CJC-1295 (GHRH pathway) and MK-677 (ghrelin pathway) may act synergistically. Different receptor targets produce complementary GH release.

GH can impair glucose tolerance. Monitor blood glucose if combining with diabetes medications.

Both are GHRH analogs acting on the same receptor. Combination provides no benefit and may cause receptor desensitization.

Both are GHRH analogs with identical mechanism. No rationale for combining; use one or the other.

Research Note: Interaction data is based on published literature, mechanistic understanding, and theoretical considerations. Most peptide combinations lack direct clinical study. This information is for educational purposes only and does not constitute medical advice. Always consult qualified healthcare providers.

References

14 Sources
4 Human
2 Preclinical

Full reference list available on request. All citations link to PubMed for verification.

Methodology Note

This dossier synthesizes available evidence from peer-reviewed literature, regulatory documents, and clinical trial registries. Evidence strength ratings follow a modified GRADE approach.

For complete methodology details, see our Methodology page.

Important Disclaimer

This dossier is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before making health decisions.

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