CJC-1295 and ipamorelin: what the blend is
CJC-1295 with ipamorelin is two different peptides sold together, and our stated PubMed search found no randomized-trial reports on them as a pair. Each was tested alone, briefly: CJC-1295 in two trials reported in one 2006 paper that measured hormone levels in healthy adults, and ipamorelin in a hospital trial that found no significant benefit over placebo. Neither is FDA-approved, and the FDA lists safety concerns for both. Through telehealth, Live Vital prices the blend at $116 a month.
What this comes down to
- The two act at different points on the growth hormone system, which is the reason given for blending them. Our stated PubMed search found no indexed randomized-trial reports on the combination.
- Two CJC-1295 trials reported in one 2006 paper raised growth hormone and IGF-I in healthy adults and reported no serious adverse reactions. It did not measure muscle, fat, sleep or recovery.
- Ipamorelin's phase 2 trial, in 114 bowel-surgery patients, found no significant difference from placebo.
- The FDA puts ipamorelin acetate on its list of compounding substances that may present significant safety risks, and says it has identified serious adverse events with CJC-1295, including increased heart rate.
- Ipamorelin25.3 hours
- Placebo32.6 hours
The difference was not statistically significant (p = 0.15).
Why are CJC-1295 and ipamorelin sold together?
Because they push on the same system from two sides. CJC-1295 is a long-acting version of growth-hormone-releasing hormone, the signal the brain uses to tell the pituitary to release growth hormone[1]. Ipamorelin works on a different receptor, the one the hunger hormone ghrelin uses, which also triggers growth hormone release[2]. Sellers combine them on the idea that two signals add up. Our stated search did not find randomized-trial reports testing that idea.
Trials of the two together. A PubMed search finds 0 results; the same search for cagrilintide with semaglutide finds 13.
What did the trials of each one find?
One 2006 publication reports two randomized, placebo-controlled CJC-1295 trials in healthy adults aged 21 to 61, lasting 28 and 49 days. A single injection raised growth hormone 2- to 10-fold for six days or more and IGF-I 1.5- to 3-fold for 9 to 11 days, and no serious adverse reactions were reported[1]. Those are hormone levels, not outcomes; nothing in the trial measured muscle, fat or how anyone felt. CJC-1295's evidence goes through it in full.
Ipamorelin was taken into a phase 2 trial by a drug company. 117 adults having bowel surgery were enrolled, and 114 were analyzed; they got ipamorelin or placebo through an IV twice a day for up to a week. The median time to a first tolerated meal was 25.3 hours on ipamorelin against 32.6 hours on placebo, and the authors found no significant difference on that or any secondary measure[2]. It is one of two randomized trials of ipamorelin in people[3]; ipamorelin's evidence covers both.
Is CJC-1295 or ipamorelin FDA-approved?
No. No approved product in the FDA's database lists either one as an active ingredient[4]. Ipamorelin acetate sits on the FDA's list of compounding substances that may present significant safety risks, added in September 2023 for the outsourcing-facility route, and CJC-1295 appears on the same page among nominations that were later withdrawn, with the agency's safety text still published[5]. Neither was part of the July 2026 advisory panel vote on peptides; are peptides legal? explains that vote, and every peptide's FDA status puts both in one table with the rest of the menu.
Approved products containing either peptide. A Drugs@FDA search finds 0 results; the same search for tesamorelin through the identical field finds 1.
What side effects have been reported?
The trials report little, because they were small and short. The two CJC-1295 trials reported in 2006 found no serious adverse reactions[1]. In ipamorelin's trial, side effects of any kind were common in both groups, 87.5% on ipamorelin and 94.8% on placebo, as expected after major surgery[2]. The FDA's own entries say more:
“FDA has identified serious adverse events associated with CJC-1295 including increased heart rate and systemic vasodilatory reaction. Available clinical data are limited.”
[5]
For ipamorelin, the agency cites a risk of immune reactions from impurities in compounded versions, and says a published study found serious adverse events, including death, when ipamorelin was given through an IV for gut motility[5]. The FDA entry links directly to the Beck 2014 study discussed above and identifies serious adverse events, including death. The abstract alone does not provide a death count or establish whether a death was caused by the drug. These findings do not establish the safety of injecting the blend under the skin at home.
Who sells CJC-1295 and ipamorelin through telehealth?
Live Vital prices the blend at $116 a month on a ten-week protocol. Blis MD and ElitePhysiqMD also name it on their menus. A telehealth prescription means a clinician reviews your health history and a licensed compounding pharmacy fills it. Websites selling the same peptides as "research use only" skip both, and the label means the product is not meant for people.
- Ask which pharmacy compounds it and check its license. Checking a compounding pharmacy shows how.
- Ask what testing each lot gets. Purity and testing for injectable peptides explains what a certificate of analysis covers.
- Compare with the alternatives on the same system: sermorelin online and tesamorelin, the one with an FDA approval.
Questions people actually ask
Has CJC-1295 with ipamorelin been tested in a clinical trial?
Our stated PubMed search found no indexed randomized-trial reports on the blend. One 2006 publication describes two trials of CJC-1295 alone. A separate ipamorelin phase 2 trial found no significant benefit over placebo.
Is CJC-1295 with ipamorelin legal?
Neither peptide is FDA-approved. The FDA lists ipamorelin acetate among compounding substances that may present significant safety risks, and publishes serious adverse events for CJC-1295. Ask the prescriber how the pharmacy is allowed to compound it.
What are the side effects of CJC-1295 and ipamorelin?
The FDA says it has identified serious adverse events with CJC-1295, including increased heart rate and a reaction in which blood vessels widen throughout the body. CJC-1295's own small trial reported no serious reactions. No side-effect rates exist for the blend.
How much does CJC-1295 with ipamorelin cost?
Live Vital prices it at $116 a month. It is the only telehealth company we review that publishes a price for the blend.
Is CJC-1295 the same as sermorelin?
No. Both mimic growth-hormone-releasing hormone, but CJC-1295 was engineered to last days, and sermorelin was once an approved drug, Geref. Neither is approved today.
Sources
Every source below was read for this article, with the claim it supports written beside it.
- 1.Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. The Journal of Clinical Endocrinology and Metabolism, 2006. PMID 16352683 · doi:10.1210/jc.2005-1536Two randomized, placebo-controlled, double-blind ascending-dose trials of 28 and 49 days in healthy adults aged 21 to 61: a single injection raised mean GH 2- to 10-fold for 6 days or more and IGF-I 1.5- to 3-fold for 9 to 11 days; no serious adverse reactions were reported. Describes CJC-1295 as a long-acting analog of GH-releasing hormone.
- 2.Prospective, randomized, controlled, proof-of-concept study of the Ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients. International Journal of Colorectal Disease, 2014. PMID 25331030 · doi:10.1007/s00384-014-2030-8Phase 2 trial of the ghrelin-receptor agonist ipamorelin, 0.03 mg/kg IV twice daily after bowel resection: 117 enrolled, 114 analyzed; treatment-emergent adverse events 87.5% vs 94.8% on placebo; median time to first tolerated meal 25.3 vs 32.6 hours (p = 0.15); no significant differences on key or secondary efficacy endpoints.
- 3.PubMed, queried through the E-utilities API. National Library of Medicine, 2026. SourceOn October 5, 2026: ipamorelin returned 2 randomized controlled trials with the human tag; CJC-1295 returned 1; the two names together returned 10 records and 0 randomized trials, against 13 for cagrilintide with semaglutide through the identical filter.
- 4.Drugs@FDA, searched by active ingredient through the openFDA API. U.S. Food and Drug Administration, 2026. SourceNo approved product lists CJC-1295, ipamorelin or ipamorelin acetate as an active ingredient; tesamorelin returns one application through the same field.
- 5.Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks. U.S. Food and Drug Administration, 2026. Source · Document dated April 2026Ipamorelin acetate is in the category 2 table (503B, September 29, 2023), citing immunogenicity risk, unnatural amino acids and a published study identifying serious adverse events including death with IV use for gastric motility. CJC-1295 is in the withdrawn-nominations table; the FDA states it has identified serious adverse events including increased heart rate and systemic vasodilatory reaction, and that available clinical data are limited.
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