C

Tier

Ipamorelin

Ipamorelin

Ipamorelin

Selective ghrelin-receptor GH secretagogue with a clean profile.

Muscle & Performance

Peptide

WADA Status:

Prohibited at all times (S2)

Human Trial Scoreboard

Completed human RCTs

0
0
0

Count not verified

Largest Human Study

0
0
0

Size not verified

Longest exposure

0
0
0

Duration not verified

Most Recent Trial

0
0
0

Year not verified

Description

Ipamorelin mimics ghrelin, the hormone your stomach releases when empty, and in doing so prompts the pituitary to release growth hormone. It was considered notable for being relatively selective, meaning it triggered less of the cortisol and prolactin response that similar compounds cause. Novo Nordisk investigated it, and it was also explored for a specific hospital problem, the sluggish return of gut function after abdominal surgery. Neither line of work produced an approved medicine. It is often grouped with sermorelin and CJC-1295 despite working through an entirely different receptor: those two imitate the growth hormone releasing signal, while ipamorelin imitates hunger. The gap between raising a hormone level and changing how a body actually looks or performs has never been closed for any compound in this group.

What Are The Claims

Claims made for this compound: Clean GH release with minimal cortisol or prolactin (human PK data); Proposed better sleep, recovery, and body composition; Selectivity is its defining feature

Evidence

The same structural gap as CJC-1295. Small human studies confirm it triggers growth hormone release. There are no outcome trials. The FDA's stated concerns are worth quoting in substance because they are technical rather than political: immunogenicity, meaning the potential for the body to mount an immune response against the peptide, and impurity characterization. Those are manufacturing and safety questions that no vendor certificate of analysis resolves.

Evidence Strength

Preliminary (small human GH-release data)

Caveats

Never approved; a Phase 2 postoperative-ileus program was discontinued after failing endpoints.

Safety
Alternative Measures
Legal Status

US

Not approved

UK

Not approved

EU

Not approved

AU

Not approved

WADA

Prohibited at all times (S2)

Not approved. Placed in FDA Category 2 in September 2023 and removed effective 27 September 2024. The FDA recommended against adding it to the 503A list at the 2024 Pharmacy Compounding Advisory Committee meetings, citing immunogenicity and impurity concerns. WADA-prohibited.

Citations

FDA Pharmacy Compounding Advisory Committee briefing materials: immunogenicity and impurity concerns. | FDA 503A Category 2, September 2023; removed 27 September 2024. | FDA recommended against 503A inclusion, 2024. | WADA Prohibited List.

The content on this site is provided for general informational purposes only and is not intended as medical advice, diagnosis, or treatment. Aambrosia sells subscription access to editorial and research content only, no supplement, compound, or other physical product discussed on this site is sold, shipped, or dispensed by Aambrosia. Always consult a qualified healthcare provider before making changes to your diet, supplement routine, or health practices. Aambrosia does not guarantee specific results, and individual outcomes may vary

Culver City California
Support: bio.aambrosia@gmail.com