Roidipedia.Compound reference & reporting
06 AUG 2026
CompoundsSARM BMS-564929
SARMNon-steroidalSARMExperimental

BMS-564929

Also known as BMS564929 · BMS-564929

BMS-564929 is an experimental non-steroidal SARM from Bristol-Myers Squibb noted in preclinical work for very high anabolic potency and strong tissue selectivity for muscle over prostate. It is highly suppressive of the HPG axis in animal models and has no established human efficacy or safety data.

01 Overview

BMS-564929 was characterised as a potent, orally active SARM with a large separation between muscle-anabolic and prostate-androgenic effects in castrated rat models. Its high potency meant active doses were low, and it markedly suppressed luteinising hormone and endogenous testosterone in animals.

BMS-564929 did not reach published human efficacy trials and is not approved. Grey-market presence is limited. Because of its potency and strong suppression in animals, extrapolated human dosing is especially uncertain, and all data remain preclinical.

02 Mechanism

Potent non-steroidal androgen receptor agonist with strong selectivity for anabolic effects in skeletal muscle over androgenic effects in the prostate in preclinical models.

03 Dosing

TierDoseRouteNotes
Anecdotal1–5 mg/dayOralHigh potency; no human data, speculative low-milligram range.

Ester comparison

EsterHalf-lifeInjection freq.Testosterone by mass

04 Effects

EffectMagnitudeEvidence
Increased muscle massPotent anabolic effect on skeletal muscle in castrated rat models.Preclinical
High tissue selectivityLarge muscle-versus-prostate selectivity margin in animals.Preclinical

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
Uncharacterised human toxicityNo human safety data; potency raises concern about narrow margins.ModerateUncharacterisedUnconfirmed
Strong HPTA suppressionPronounced suppression of LH and endogenous testosterone in animal models.SevereMarked in animalsPreclinical

07 References

Discovery and characterization of BMS-564929, a novel muscle-selective androgen receptor modulatorJournal of Medicinal Chemistry / Endocrinology, 2007

08 Discussion0 comments

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