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Description

Regulatory measures, from the FDAs Compounding Risk Alert to DOJ prosecutions of pharmacies that dispensed unapproved peptides, cement the narrative that access and quality are legitimate issues

Phase 1 oral trial, and a small retrospective knee-pain case series without blinding

The pharma has previously announced that REDEFINE 1 is expected to read out by the end of the year, while data from REDEFINE 2 are expected in the first half of 2025