Studied for gut healing, tissue and tendon repair, and anti-inflammatory effects.
AAPM (American Academy of Peptide Medicine) works on both sides of peptide medicine: the policy decisions that determine whether Americans can obtain peptide therapies, and the clinical and quality standards that keep those therapies safe once they do.
Advocating to place these peptides in Category 1 so patients can obtain them through licensed U.S. compounding pharmacies, under a valid prescription and physician oversight.
Replacing unregulated online and international sources with regulated channels held to USP 795 and 797 standards for sterility, potency, and purity.
Each September, AAPM (American Academy of Peptide Medicine) convenes clinicians, researchers, and policymakers for scientific programming, peer exchange, and direct policy engagement in the nation's capital.
The FDA Pharmacy Compounding Advisory Committee reviewed seven peptides and voted to recommend six for the 503A bulks list. The FDA now makes the final call through formal rule-making.
Studied for gut healing, tissue and tendon repair, and anti-inflammatory effects.
A Thymosin Beta-4 fragment studied for muscle repair and recovery.
A tripeptide with documented anti-inflammatory and gut-supportive properties.
A mitochondrial-derived peptide studied for metabolic regulation.
Delta sleep-inducing peptide, studied for sleep and stress response.
Studied for cognitive support and neuroprotection.
Studied for cellular aging and circadian regulation.
A committee recommendation is not FDA approval and does not change access rules on its own. These compounds remain prescription-only and require individualized physician evaluation through a licensed provider and an accredited compounding pharmacy.
See the full resultsThe 2023 restrictions did not eliminate demand. They eliminated regulation. This is the path back to physician-supervised, regulated access.
14 widely used peptides are placed on the Category 2 restricted list, pushing patients toward unregulated sources.
HHS signals intent to begin restoring safe, physician-supervised, legally compounded access.
Peptides are formally removed from the do-not-compound list, effective within seven calendar days.
At its hearing on the FDA White Oak Campus, the PCAC votes to recommend six of seven peptides for the 503A bulks list.
The FDA weighs the recommendation in formal rule-making. AAPM keeps pressing for a final rule that restores regulated access.
Our founding advisory board includes former governors from both parties, signaling that patient access to safe peptide medicine transcends party lines.
Our board pairs practicing physicians, pharmacists, and nurses with FDA regulatory attorneys, pharmacy law experts, and former state officials.
Each September, AAPM (American Academy of Peptide Medicine) convenes physicians, researchers, and policymakers in Washington, D.C. for scientific programming and direct policy engagement.