Tesamorelin/Ipamorelin
WHAT IT IS
Growth Hormone Secretagogues
BEST FOR
Pentapeptide Ghrelin-Mimetics, Selective for GH Release
HOW IT'S USED
Growth Hormone-Releasing Peptides (GHRPs)
WHY CHOOSE IT
Discontinued clinical development; now an unregulated "research chemical" market
$ 294.00 USD
3MG/2MG/ML
Description
Molecular Profile
Ipamorelin
Selective GHRP — ghrelin receptor agonist
Sequence Aib-His-D-2-Nal-D-Phe-Lys-NH₂ (5 amino acids)
Class Synthetic ghrelin receptor agonist, engineered for greater target selectivity than older GHRPs (e.g. GHRP-6)
Form Subcutaneous injectable Typically compounded; frequently paired with CJC-1295
Developer Novo Nordisk
Clinical history Studied through Phase 2 for postoperative ileus Trial failed primary endpoint Beck et al., 2014 — Novo Nordisk discontinued development
HOW IT WORKS

Ipamorelin binds the ghrelin receptor (GHS-R) in the pituitary, triggering a pulsatile release of the body's own growth hormone. Its defining feature relative to earlier ghrelin-mimetic peptides is selectivity — in preclinical models it stimulates GH release with comparatively little effect on cortisol, prolactin, or appetite, the off-target effects that limited older secretagogues.

WHAT TO EXPECT
  • Formerly investigated for postoperative gastrointestinal motility (discontinued)
  • Widely used off-label/informally, often stacked with CJC-1295, in longevity and bodybuilding-adjacent GH-optimization protocols
  • Sold exclusively through "research chemical" channels; no legal compounding pathway as of early 2026
BEFORE YOU START
  • Placed in FDA Category 2 (restricted, no compounding) in September 2023; as of April 2026 no compounding pharmacy may legally prepare it for human use
  • Named among peptides referred to the Pharmacy Compounding Advisory Committee alongside CJC-1295, with a possible path back to Category 1 signaled by HHS in February 2026 — but as of the most recent published guidance, no formal reclassification had taken effect
  • Prohibited under the WADA Prohibited List (Class S2) — same status as MOTS-c and Tesamorelin in this collection
  • Its only completed human RCT failed to meet its endpoint; unlike tesamorelin, it has never advanced through Phase
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