REGULATORYRFK Jr.: 14 peptides returning to Category 1 — FDA advisory committee July 2026TRENDINGHexarelin: ↑↑ Surging ��� Trends score 100 as of May 2026UPDATESemaglutide and tirzepatide compounding ended — shortage resolved Feb/May 2025REGULATORYBPC-157, TB-500, thymosin alpha-1, CJC-1295, ipamorelin: expected Category 1 reclassification pendingEVENTpep-talk con ��� First US Peptide Convention · August 2026 · Anaheim CAFDAFDA advisory committee meetings scheduled: late July 2026REGULATORYRFK Jr.: 14 peptides returning to Category 1 — FDA advisory committee July 2026TRENDINGHexarelin: ↑↑ Surging ��� Trends score 100 as of May 2026UPDATESemaglutide and tirzepatide compounding ended — shortage resolved Feb/May 2025REGULATORYBPC-157, TB-500, thymosin alpha-1, CJC-1295, ipamorelin: expected Category 1 reclassification pendingEVENTpep-talk con ��� First US Peptide Convention · August 2026 · Anaheim CAFDAFDA advisory committee meetings scheduled: late July 2026

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Peptide Library

Ipamorelin

NNC 26-0161

Growth Hormone Secretagogues

Ipamorelin is a highly selective pentapeptide growth hormone secretagogue that acts on the ghrelin/GHS receptor to stimulate pulsatile GH release from the anterior pituitary. Developed by Novo Nordisk in the 1990s, it is distinguished from other GHRPs by its remarkable selectivity, producing GH release without significantly affecting cortisol, prolactin, or aldosterone levels. It is considered the most well-tolerated GHRP available and is a cornerstone of modern GH optimization research protocols.

Mechanism of Action

Selective growth hormone secretagogue receptor (GHSR) agonist. Stimulates pituitary GH release with minimal effect on cortisol, prolactin, or ACTH. One of the most selective ghrelin mimetics available, producing clean GH pulses without appetite stimulation.

Research Protocols

For research purposes only. Not medical advice.

Research protocols use 100-300mcg 2-3 times daily via subcutaneous injection. Best administered on an empty stomach. Often combined with CJC-1295 for synergistic GH release. Cycles of 8-16 weeks.

Research Notes

Clinical Research Status

Ipamorelin completed Phase 2 clinical trials for post-operative ileus (gut motility recovery) but was not advanced to approval. Published human studies confirm dose-dependent GH release with minimal effect on other pituitary hormones. It remains widely used in clinical research and anti-aging medicine despite lacking FDA approval for any indication.

Key Published Findings

Studies demonstrate that Ipamorelin produces GH release comparable to GHRP-6 and GHRP-2 at equivalent doses without the cortisol and prolactin elevation seen with those compounds. Research shows it does not significantly stimulate appetite (unlike GHRP-6 and hexarelin) due to weaker ghrelin receptor activation in appetite centers. Clinical trials documented improved bowel recovery time in post-surgical patients.

Safety Profile

Ipamorelin has the cleanest side effect profile among all GHRPs, with minimal reports of water retention, hunger stimulation, or cortisol elevation at standard doses. Transient headache, flushing, and mild dizziness may occur in the first 1-2 weeks of use. No significant adverse cardiovascular or metabolic effects have been documented in published trials at therapeutic doses.

Drug Interactions & Contraindications

Should not be used concurrently with somatostatin or its analogs. Caution advised when combining with insulin or insulin secretagogues due to GH's diabetogenic effects. Contraindicated in active malignancy and untreated pituitary tumors. May reduce efficacy of glucocorticoids through GH-mediated cortisol suppression at high doses.

Comparison to Related Compounds

Compared to GHRP-6, Ipamorelin produces equivalent GH release without significant hunger or cortisol elevation. Compared to GHRP-2, it has slightly lower maximal GH output but substantially fewer side effects. Hexarelin produces the highest GH response among GHRPs but causes significant cortisol/prolactin release and desensitizes within weeks, making Ipamorelin preferred for longer protocols.

Community Observations

Standard research dosing is 100-300mcg subcutaneously 1-3 times daily, typically combined with Modified GRF(1-29) at equal doses for synergistic GH release. Most commonly administered before sleep to augment the natural nocturnal GH pulse. Users consistently report improved sleep quality, recovery, and gradual body composition improvements with minimal side effects over 3-6 month protocols.

Half-Life

~2 hours

Reconstitution

Bacteriostatic water (BAC)

Storage

Lyophilized

Refrigerate 2-8C up to 24 months.

Reconstituted

Refrigerate 2-8C. Use within 21 days.

US Legal Status

Research chemical (not FDA-approved)

Also Known As

NNC 26-0161

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