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February 13, 2026The Journal of Clinical Endocrinology & Metabolism2 citations

Will Selective Androgen Receptor Modulators Ever Reach The Clinic?

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JDJenny Pena DiasADA. S. Dobs

Key Points

  • The research aims to explore the clinical applicability of selective androgen receptor modulators (SARMs) for various conditions.
  • Reviewed the chemical properties of SARMs and their mechanisms of action.
  • Analyzed clinical trial results regarding efficacy in increasing lean body mass.
  • Assessed safety concerns associated with SARMs, particularly hepatotoxicity and cardiovascular risks.
  • Multiple SARMs have been effective in increasing lean body mass during clinical trials.
  • Few SARMs showed consistent improvements in strength or mobility metrics.
  • Safety concerns regarding long-term use and potential side effects remain unresolved.

Abstract

Abstract Selective androgen receptor modulators (SARMs) are a novel class of compounds engineered to confer the anabolic benefits of testosterone such as increased muscle and bone mass while minimizing undesirable androgenic effects. Their tissue-selective activity and oral availability have sparked significant interest in their potential applications for conditions like muscle wasting, osteoporosis, hypogonadism, and frailty. We outline the chemical underpinnings of SARMs, their clinical promise, and the major challenges that have limited their regulatory approval to date. Although multiple SARMs have shown efficacy in increasing lean body mass in clinical trials, few have demonstrated consistent improvements in functional outcomes such as strength or mobility. Safety concerns, particularly regarding hepatotoxicity and cardiovascular risk, remain incompletely resolved. Nevertheless, a subset of SARMs is being actively evaluated for indications directly related to aging and sarcopenia. We conclude that SARMs are likely to enter clinical practice in select niches of men and women, especially among the frail, the elderly, or individuals with excessive loss of lean body mass. However, widespread approval will depend on future trials demonstrating both efficacy and long-term safety.

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Cite This Study

Dias et al. (2026) studied this question.

synapsesocial.com/papers/698ebf4385a1ff6a93016847https://doi.org/10.1210/clinem/dgaf700
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Activity and safety of enobosarm, a novel, oral, selective androgen receptor modulator, in androgen receptor-positive, oestrogen receptor-positive, and HER2-negative advanced breast cancer (Study G200802): a randomised, open-label, multicentre, multinational, parallel design, phase 2 trial2024 · 48 citations
  2. 2Design, Synthesis, and Preclinical Characterization of the Selective Androgen Receptor Modulator (SARM) RAD1402010 · 72 citations
  3. 3A First-in-Human Phase 1 Study of a Novel Selective Androgen Receptor Modulator (SARM), RAD140, in ER+/HER2- Metastatic Breast Cancer2021 · 23 citations
  4. 4A phase IIA randomized, placebo-controlled clinical trial to study the efficacy and safety of the selective androgen receptor modulator (SARM), MK-0773 in female participants with sarcopenia2013 · 197 citations
  5. 5Testosterone Supplementation in Older Men: A Rational Idea Whose Time Has Not Yet Come2001 · 137 citations