18+ • For Research & Educational Purposes Only • Not Medical Advice  Disclaimer
Peptide Wiki
PerformancePhase 2

RAD-140

Highly selective SARM with strong anabolic-to-androgenic ratio and notable neuroprotective effects via PI3K/Akt pathway

Research Reality Check

Worth WatchingThere is a real signal, but it is not settled.
ClaimSome people claim RAD-140 has clear value for performance research.
RealityThere is a real research signal, but important questions remain.
Bottom LineUse the evidence score, sources, and safety notes before taking any claim seriously.
Why People Believe ThisSimple explanations and user stories can sound more certain than the research is.
Watch Out For
Guaranteed resultsExact protocols presented as provenAnecdotes used as proof
834Discussions
2Citations

Evidence Dossier

82Evidence

Phase 2

Evidence score reflects source depth, citations, and research maturity. It is not a medical recommendation.

2Citations
834Discussions
Start Here

RAD-140 at a glance

A fast read for beginners, with evidence strength, route context, safety depth, and community activity surfaced before the deeper sections.

Evidence score82Phase 2 human research
Primary routeOralRoute availability varies by context
Safety depthLimited dataReview safety notes before making assumptions
Community questions834Related discussions and experiences

RAD-140 (Testolone) is a non-steroidal selective androgen receptor modulator developed by Radius Health. It demonstrates one of the highest anabolic-to-androgenic selectivity ratios of any SARM studied - in animal models it has outperformed testosterone in stimulating muscle growth at doses that produce no prostate stimulation.

How It Works

In a primate study, RAD-140 increased lean mass significantly with no prostate growth and no liver toxicity at effective doses. Phase 1 and 2 clinical trials in breast cancer (AR+/ER+ metastatic) have demonstrated partial responses and disease stabilization, with manageable side effects. Testosterone suppression is significant at doses used in performance settings (10-20mg), requiring post-cycle therapy.

A distinctive feature of RAD-140 versus other SARMs is its neuroprotective activity: it activates MAPK/PI3K/Akt signaling in neurons, reducing Alzheimer's-related amyloid beta toxicity and neuronal apoptosis in preclinical models. This dual anabolic/neuroprotective profile has generated significant scientific interest. It remains unapproved for any indication outside of oncology trials and is WADA-banned.

Key Benefits

High anabolic-to-androgenic selectivity
Lean muscle mass gains
Strength
Neuroprotection (preclinical)
Bone density support