Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Head-to-head comparison of Capromorelin and CJC-1295 — mechanism, side effects, legal status, and pricing.
Capromorelin is a non-peptide, orally active pyrazolinone-piperidine dipeptide-mimetic that functions as a growth hormone secretagogue receptor 1a (GHS-R1a) agonist, mimicking the endogenous hormone ghrelin. It is NOT approved for human use anywhere; a Pfizer Phase II trial in 395 older adults showed positive signals for lean body mass, body weight, and physical function but was terminated early and never advanced to approval. Capromorelin is FDA-approved as a veterinary drug (Entyce for dogs, Elura for cats) and is explicitly named on the WADA Prohibited List under S2 (growth hormone secretagogues), prohibited at all times in competitive sport.
CJC-1295 is a synthetic tetrasubstituted analog of growth hormone-releasing hormone (GHRH 1-29) originally developed by ConjuChem. The name historically refers to the DAC-modified (Drug Affinity Complex) form that covalently binds serum albumin, producing a 6–8 day half-life; a separate no-DAC form (also called Modified GRF 1-29) shares the same tetrasubstituted backbone but lacks the albumin-linking maleimidopropionyl-lysine and has a half-life of roughly 30 minutes. Not FDA-approved in any form; ConjuChem halted Phase 2 development around 2007 after a patient death in an HIV-lipodystrophy trial (ultimately judged by investigators to be unrelated to the drug, but development was terminated regardless).
Capromorelin
CJC-1295
Category
Legal Status
Mechanism
Half-life
Side Effects
COA-verified vendors · trust score ≥70 required · single-vial price — bulk/bundle deals may be lower
Capromorelin
CJC-1295
COA corpus from Disclosed Labs — independently tested batches only.
Capromorelin
No COA data yet.
Submit testing data →CJC-1295
115
COAs
98.8%
Avg purity
12
Labs
CJC-1295 is among peptides under FDA review for the Category 1 (503A) list; if added, it would require a prescription to be compounded by registered 503A/503B pharmacies — not yet authorized. Capromorelin remains research-only. In April 2026 the FDA removed 12 peptides from Category 2, which does not place them on the Category 1 list or authorize compounding. The FDA's Pharmacy Compounding Advisory Committee is advisory and meets July 23–24, 2026 to review nominations and make recommendations to the FDA.
Capromorelin has human clinical trial data but is not an approved human drug. A Pfizer-sponsored Phase II trial randomized 395 adults aged 65–84 at risk of functional decline to oral capromorelin or placebo for up to 2 years (315 completed 6 months; 284 completed 12 months). The trial reported increased lean body mass (+1.4 vs 0.3 kg, P=0.001), body weight (+1.4 kg, P=0.006), improved tandem walk (P=0.02), and improved stair climb (P=0.04), concluding capromorelin "may improve body composition and physical function." The study was terminated early according to predetermined treatment effect criteria; no human product was ever approved. Preclinical studies in rats showed an ED50 <0.05 mg/kg IV for plasma GH elevation; in healthy Beagle dogs, oral capromorelin increased food consumption and body weight in a 4-day randomized, masked, placebo-controlled trial. In healthy cats, capromorelin altered glucose-metabolism parameters. In broiler chickens, it increased feed intake and body-weight gain.
Key references
In healthy adults, single SubQ doses of CJC-1295 (with DAC) elevated plasma GH 2- to 10-fold for ≥6 days and IGF-1 1.5- to 3-fold for 9–11 days (Teichman et al., JCEM 2006), and pulsatile GH secretion was preserved rather than suppressed during continuous stimulation (Ionescu & Frohman, JCEM 2006). Despite these Phase 1/2 findings, ConjuChem halted Phase 2 lipodystrophy development in 2006–2007 after a trial participant died of a myocardial infarction; the event was deemed most likely due to pre-existing coronary disease, but the program was not resumed. No CJC-1295 form is FDA-approved for any indication. Grey-market use almost always refers to the no-DAC / Modified GRF 1-29 form, often stacked with ipamorelin; neither variant is clinically validated for anti-aging, body composition, or performance indications.
Capromorelin (Hormone) and CJC-1295 (Performance) are in different categories and target different biological pathways. This is a common pattern in multi-compound research protocols. Researchers should monitor the biomarkers from both profiles and watch for interactions listed in each compound’s contraindications. Consult a licensed healthcare provider before combining any research compounds.
This platform provides informational tools only, not medical advice. This comparison is for educational purposes only. Consult a licensed provider.
Contraindications
Lab Testing
Key references
Disclosed Labs