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SARM

Ostarine

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Overview

The most clinically studied SARM, evaluated for muscle wasting and cancer cachexia in Phase 2 trials, but never approved.

How it works

Ostarine (enobosarm) is the most clinically studied SARM — a 'selective androgen receptor modulator.' Like testosterone it acts on the androgen receptor, but it's designed to be tissue-selective.

The goal of that selectivity is to switch on the muscle- and bone-building effects of androgen signaling while having less effect on tissues like the prostate and skin. The selectivity is thought to come from the shape the receptor takes when this drug binds and which helper proteins it recruits, and in trials it did increase lean body mass.

The selectivity is only partial, though: trials and reports still show suppression of the body's own testosterone (the HPTA axis), lowered HDL cholesterol, and sometimes raised liver enzymes. It is not approved for any use and is banned in sport.

Mechanism · Detailed Analysis
Molecular targetA nonsteroidal selective androgen-receptor (AR) agonist with tissue-selective activation — anabolic in muscle and bone, with lower activity in prostate and skin.
Signaling & downstream effectsAR-mediated transcription drives muscle protein synthesis and bone formation; tissue selectivity is attributed to differential AR conformation and coregulator recruitment.
PharmacokineticsOral, with a roughly 24 h half-life.
CaveatsDespite selectivity, trials and reports show testosterone/LH/FSH (HPTA) suppression, reduced HDL, and liver-enzyme elevations. Not approved; banned in sport.
Published EvidenceLoading cited studies from PubMed…
Human Data ···

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Animal ···

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In Vitro ···

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Educational aggregation of public literature. Not medical advice and not a recommendation to use any compound. Many compounds here are not approved for human use. Consult a licensed clinician.