CJC-1295 (No DAC)
Also known as: CJC-1295 DAC, CJC-1295 no DAC, Modified GRF 1-29
Key Facts: CJC-1295 (No DAC)
- Category
- Growth Hormone
- FDA Status
- Not FDA Approved
- Clinical Status
- Investigational - Phase II trial discontinued. Removed from FDA Category 2 in Sept 2024 for PCAC review; expected reclassification to Category 1 (April 15, 2026 HHS announcement; remains Category 2 under current law until formal FDA rule; PCAC review July 23-24, 2026)
- Administration
- Subcutaneous injection
- Typical Dose
- 100 mcg daily (no DAC) or 2 mg weekly (with DAC)
- Frequency
- Daily (no DAC) or 1-2x weekly (with DAC)
- Duration
- 8-12 weeks
Mechanism of Action
CJC-1295 acts at the GHRH receptor on pituitary somatotroph cells, the same receptor the body's own GHRH uses, prompting the pituitary to synthesize and release growth hormone. Native GHRH is broken down within minutes; CJC-1295 with DAC carries a reactive group that covalently bonds to circulating albumin after injection, shielding it from breakdown and stretching its half-life from minutes to days. The sustained GH elevation drives the liver to produce IGF-I, the downstream hormone behind many of GH's tissue effects. There are two versions: with DAC (long-acting, albumin-binding) and without DAC (Modified GRF 1-29), which lacks the albumin tether. Because it works through the pituitary, it relies on the gland's own GH-producing capacity.
Research Summary
The key human study is Teichman et al. (2006) in the Journal of Clinical Endocrinology and Metabolism, a randomized, double-blind, placebo-controlled ascending-dose trial in healthy adults. A single subcutaneous injection raised mean plasma GH 2- to 10-fold for 6 days or more and IGF-I 1.5- to 3-fold for 9 to 11 days, with cumulative effects on repeat dosing, and was reported as safe and relatively well tolerated short-term. An earlier study showed once-daily CJC-1295 normalized growth in GHRH-knockout mice. Beyond pharmacokinetics and hormone levels, there are no large long-term human trials demonstrating clinical benefits like fat loss or muscle gain, so those claims are not established by published trials. Development was halted after Phase II; a single trial death was attributed by the attending physician to pre-existing coronary artery disease rather than the drug, which is reported but not independently confirmed. Bottom line: the GH and IGF-I-raising effect and long half-life are well supported, while real-world efficacy and long-term safety are not.
Dosing Information
Typical Dosingⓘ
Community experience
100 mcg daily (no DAC) or 2 mg weekly (with DAC)
100-300 mcg per dose (no DAC), 1-2 mg weekly (DAC)
Daily (no DAC) or 1-2x weekly (with DAC)
No-DAC version requires daily dosing. DAC version has longer half-life. Often stacked with GHRP like Ipamorelin.
Research Dosingⓘ
Scientific studies
Doses observed in research studies
Doses from Studies
CJC-1295 DAC: 1-2mg weekly
Mod GRF 1-29: 100-300 mcg 2-3x daily
Duration
8-12 weeks
Administration
Subcutaneous injection
Timing & Administration
Best Time to Take
Before bed
1-2 times per week
Food Recommendation
Take on empty stomach
Why This Timing?
CJC-1295 (with DAC) has a long half-life (~8 days) so timing is less critical, but evening dosing supports natural GH patterns.
Possible Side Effects
Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.
- ●Generally well-tolerated
- ●Injection site reactions
- ●Facial flushing
- ●Headache
- ●Water retention
- ●Dizziness
- ●May trigger histamine release - use caution with MCAS or histamine sensitivity
- ●Concerns for cancer patients (IGF-1/GH effects)
- ●Risk of immunogenicity
References
- https://pubmed.ncbi.nlm.nih.gov/16352683/
- https://pubmed.ncbi.nlm.nih.gov/17018654/
- https://pubmed.ncbi.nlm.nih.gov/15817669/
Research This Peptide Further
Frequently Asked Questions
What does CJC-1295 (No DAC) do?
CJC-1295 is a synthetic analog of growth hormone-releasing hormone (GHRH), specifically a modified GHRH(1-29), engineered for a long duration of action. The form most people mean by CJC-1295 includes a Drug Affinity Complex (DAC) that binds blood albumin to extend its half-life to roughly 6 to 8 days, raising GH and IGF-I for days from a single injection. It was developed by ConjuChem, reached Phase II trials and was abandoned; it is not an approved drug and is sold only as a research chemical. A version without DAC (Modified GRF 1-29) acts for only about 30 minutes.
How does CJC-1295 (No DAC) work?
CJC-1295 acts at the GHRH receptor on pituitary somatotroph cells, the same receptor the body's own GHRH uses, prompting the pituitary to synthesize and release growth hormone. Native GHRH is broken down within minutes; CJC-1295 with DAC carries a reactive group that covalently bonds to circulating albumin after injection, shielding it from breakdown and stretching its half-life from minutes to days. The sustained GH elevation drives the liver to produce IGF-I, the downstream hormone behind many of GH's tissue effects. There are two versions: with DAC (long-acting, albumin-binding) and without DAC (Modified GRF 1-29), which lacks the albumin tether. Because it works through the pituitary, it relies on the gland's own GH-producing capacity.
Is CJC-1295 (No DAC) FDA approved?
No, CJC-1295 (No DAC) is not currently FDA approved. Current status: Investigational - Phase II trial discontinued. Removed from FDA Category 2 in Sept 2024 for PCAC review; expected reclassification to Category 1 (April 15, 2026 HHS announcement; remains Category 2 under current law until formal FDA rule; PCAC review July 23-24, 2026)
What are the side effects of CJC-1295 (No DAC)?
Reported side effects include: Generally well-tolerated, Injection site reactions, Facial flushing, Headache, Water retention. Individual responses vary based on dosage, duration, and personal health factors.
What is the typical dose of CJC-1295 (No DAC)?
Community-reported common dose: 100 mcg daily (no DAC) or 2 mg weekly (with DAC) (Daily (no DAC) or 1-2x weekly (with DAC)). Range: 100-300 mcg per dose (no DAC), 1-2 mg weekly (DAC). Administration: Subcutaneous injection. Community-reported doses. Not medical advice. Consult healthcare provider.
Related Peptides
Peptides commonly compared with CJC-1295 (No DAC) or used in similar applications.
Ipamorelin
Clinical TrialsIpamorelin is a synthetic pentapeptide growth hormone secretagogue developed by Novo Nordisk and derived from GHRP-1. It is researched mainly for stimulating the body's own growth hormone (GH) release, and was studied in humans primarily for postoperative ileus and gut motility rather than anti-aging. It is not an approved drug anywhere: it reached Phase II trials, was discontinued for insufficient efficacy, and is now sold only as a research chemical.
Growth HormoneGHRP-6
Clinical TrialsGHRP-6 is a synthetic six-amino-acid peptide (His-D-Trp-Ala-Trp-D-Phe-Lys-NH2) that tricks the body into releasing its own growth hormone. It was one of the first growth hormone secretagogues ever made, and the hunt to find out why it worked led scientists straight to the discovery of ghrelin. It has no approval as a drug anywhere and is used only as a research compound.
Growth HormoneGHRP-2
Clinical TrialsGHRP-2 (generic name pralmorelin) is a synthetic hexapeptide growth hormone secretagogue and a second-generation cousin of GHRP-6. It prompts the pituitary to release growth hormone and is the one peptide in this family with an actual regulatory approval: it is licensed in Japan as a diagnostic agent for growth hormone deficiency. Outside that narrow diagnostic use it has no approval and is sold elsewhere only as a research compound.
Growth HormoneMK-677
Clinical TrialsMK-677 (ibutamoren) is not actually a peptide, it is a small, orally active non-peptide molecule that mimics ghrelin, your hunger and growth-hormone hormone. Taken as a daily pill, it reliably pushes up growth hormone and IGF-1 levels, which is why it is popular for muscle and recovery. It has been through real human trials but was never approved as a drug, and the trials that mattered most for older adults and Alzheimer's came up short.
Growth HormoneTesamorelin
FDATesamorelin is a stabilized analog of growth-hormone-releasing hormone (GHRH 1-44) with a chemical modification that protects it from rapid breakdown. It is FDA-approved (brand name Egrifta) to reduce excess visceral abdominal fat in people with HIV-associated lipodystrophy, which makes it one of the few growth-hormone-axis peptides with a real approval behind it. Its evidence base is solid for that specific population and thinner for the general anti-aging and fat-loss uses it gets promoted for online.
Growth HormoneSermorelin
PreclinicalSermorelin is a 29-amino-acid fragment of human growth hormone-releasing hormone (GHRH), and it is the shortest piece of GHRH that still works fully. It asks the pituitary to make and release its own growth hormone rather than injecting GH itself. It was once an FDA-approved drug for diagnosing and treating growth hormone deficiency in children, but the manufacturer pulled it from the market in 2008, so today it is available mainly through compounding pharmacies for off-label use.
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