CJC-1295 with DAC results: what to expect and when
An experimental long-acting peptide that triggers growth hormone release, with no proven muscle or recovery benefit.
Also called: CJC-1295 DAC, DAC:GRF, DAC-GRF.
GHRH analogues · Long-acting GHRH receptor agonist with an albumin-binding tag.
Three small published studies and one stopped HIV trial. A protein report reused participants; health benefits remain unproven.
Key studies
- Teichman 2006: one dose: One DAC injection raised GH and IGF-1 for days; it did not test muscle gain, fat loss or recovery. (source)
- Teichman 2006: repeat doses: Weekly or fortnightly DAC dosing accumulated and kept IGF-1 elevated; long-term outcomes were not tested. (source)
- Ionescu 2006: GH pulses: DAC preserved detectable GH pulses while raising the trough; this does not prove safety of sustained stimulation. (source)
- Sackmann-Sala 2009: blood proteins: An exploratory analysis found possible hormone-response markers, not better health or performance. (source)
- HIV visceral-fat trial: terminated: The terminated study supplies no usable benefit estimate or established safe weekly maximum. (source)
- Jetté 2005: albumin binding: Animal and cell work supports a long-lasting GHRH analogue; it does not validate community products. (source)
Related to CJC-1295 with DAC
- CJC-1295 without DAC: A peptide intended to trigger growth hormone release, with no human dosing study found.
- Tesamorelin: A peptide approved for deep abdominal fat in adults with HIV lipodystrophy.
- Sermorelin: An experimental short-acting peptide that triggers growth hormone release, with limited evidence of adult benefits.
- Ipamorelin: An experimental peptide that triggers growth hormone release.
Sources
- 21 CFR 216.23 — Bulk drug substances that can be used to compound drug products in accordance with section 503A of the Federal Food, Drug, and Cosmetic Act., Office of the Federal Register · eCFR · 2026
- 503B Bulk Drug Substances List, FDA · FDA · 2026
- Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks, FDA · FDA · 2026
- Concerns regarding the public health risks associated with unapproved peptide products, Therapeutic Goods Administration and Chief Medical Officer · Therapeutic Goods Administration · 2026
- Medicines, European Medicines Agency · European Medicines Agency · 2026
- The 2026 Prohibited List, World Anti-Doping Agency · WADA · 2026
- Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026, Australian Government · Australian Government · 2026
- Think twice before injecting peptides bought online: unauthorized products can seriously harm you, Health Canada · Health Canada · 2026
- EGRIFTA WR (tesamorelin) for injection, for subcutaneous use, U.S. Food and Drug Administration · FDA · 2025
- Supply unlicensed medicinal products (specials), MHRA · 2025
- December 4, 2024 Pharmacy Compounding Advisory Committee Meeting, FDA · 2024
- FDA Briefing Document Pharmacy Compounding Advisory Committee (PCAC) Meeting December 4, 2024, US Food and Drug Administration · 2024
- Anticoagulant medicines - Side effects, NHS
- DailyMed - GLUCOTROL XL- glipizide tablet, extended release, Pfizer Inc. · DailyMed
- Know When to Go to the ER, American College of Emergency Physicians · American College of Emergency Physicians
Sources checked: 2026-10-18.
Information only, not medical advice. Peptifacts does not sell anything and does not link to sellers.