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
| Tier | Dose | Route | Notes |
|---|---|---|---|
| Anecdotal | 1–5 mg/day | Oral | High potency; no human data, speculative low-milligram range. |
Ester comparison
| Ester | Half-life | Injection freq. | Testosterone by mass |
|---|
04 Effects
| Effect | Magnitude | Evidence | |
|---|---|---|---|
| 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
| Effect | Severity | Frequency | Evidence | Countermeasures |
|---|---|---|---|---|
| Uncharacterised human toxicityNo human safety data; potency raises concern about narrow margins. | Moderate | Uncharacterised | Unconfirmed | |
| Strong HPTA suppressionPronounced suppression of LH and endogenous testosterone in animal models. | Severe | Marked in animals | Preclinical |