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Hormones & endocrine-related compounds

Testolone

Vosilasarm (RAD140)

Testolone (RAD140, vosilasarm) is an investigational selective androgen receptor modulator, or SARM. Healthy-user cognitive and performance benefits are unproven, while serious liver-injury reports and FDA warnings warrant high caution. Compare listed identity and total labeled amount, verify retailer prices, and distinguish research-product labels from evidence of a safe dose.

Hormonal Axis RelatedSyntheticClinical ResearchLimited Human EvidenceMostly Animal EvidenceInsufficient EvidenceHigh Risk Profile
Updated October 2026/6 min read/9 citations
Reviewed by the NootropicsIndex editorial team.Method: prioritize cited human research and official safety or regulatory sources; compare retailer-listed prices without endorsing products.Affiliate disclosure
01

What is it?

What Testolone is

1

Testolone is the common marketplace name for RAD140, also listed as vosilasarm. It is a nonsteroidal selective androgen receptor modulator, or SARM, developed as an investigational drug-like compound rather than a dietary supplement ingredient.

Evidence boundary2
The strongest public human RAD140 evidence is a small Phase 1 oncology study in postmenopausal women with metastatic breast cancer. That does not validate healthy-user bodybuilding, nootropic, cycle, or daily supplement claims.
02

Names, aliases and forms

Common NameTestolone
Research CodesRAD140; RAD-140
Inn NameVosilasarm
Cas Number1182367-47-0
03

Mechanisms of action

Mechanism context

2

RAD140 was designed to bind androgen receptors and produce tissue-selective androgenic signaling. Preclinical work describes anabolic androgen action models, and the Phase 1 study tracked SHBG and PSA as markers of androgen receptor engagement. Mechanism should not be read as proof of consumer performance or cognitive benefit.

04

Potential effects and evidence map

RAD140 has preclinical SARM research and a first-in-human Phase 1 study in postmenopausal women with ER+/HER2- metastatic breast cancer. That study reported once-daily dose levels, androgen receptor engagement markers, a 44.7-hour The time for blood levels to fall by half during the final elimination phase.Source, and frequent treatment-emergent adverse events including liver enzyme and bilirubin elevations. This is not evidence for healthy-user cognition, strength, or supplement-style cycle claims.

Effect domainMagnitudeGrade
Physical energy / endurance4
UnknownConfidence: Low

RAD140 has preclinical anabolic androgen receptor research, but public human evidence does not establish healthy-user strength, endurance, or performance benefits.

Note Do not convert SARM mechanism or bodybuilding marketing into a proven consumer performance claim.

0/5
D
Focus / attention2
UnknownConfidence: High

No reliable human evidence was found that Testolone/RAD140 improves focus, attention, memory, mood, or nootropic outcomes.

Note Legacy nootropic claims should not be repeated without human data.

0/5
E
Libido / vitality2
UnknownConfidence: Low

Androgen receptor engagement markers in an oncology study do not establish consumer libido or vitality benefits.

Note Keep androgen receptor pharmacology separate from wellness claims.

0/5
E
05

Typical dosages and timing

Oncology trial doses250-150 mg/day

In 22 postmenopausal women with metastatic breast cancer, the Phase 1 study evaluated 50, 100, and 150 mg once daily; the maximum tolerated dose in that protocol was 100 mg/day. These are oncology research doses, not a safe consumer range. No evidence-based healthy-adult supplement dose or cycle has been established.

06

Timing & effect horizon

Effect horizonUnknown
Unknown
Half-life2Acute
44.7 hours
Time course2

The Phase 1 study reported a 44.7-hour half-life, which supported once-daily dosing in that clinical protocol. Public sources checked did not establish healthy-user effect onset, acute duration, washout timing, or cycle timing.

07

Safety, side effects and risk profile

Legal / regulatory risk6
Confidence: High

As of 14 October 2026, U.S. FDA states SARMs cannot legally be marketed as dietary supplements or approved drugs. Separate WADA anti-doping restrictions apply in governed sport.

Note Keep legal wording jurisdiction- and context-scoped; marketplace availability is not approval.

4/5
A
Liver / kidney caution8
Confidence: Medium

Serious liver injury has been reported after oral RAD140 use in previously healthy adults. Its frequency is unknown, and case reports cannot fully separate compound toxicity from product quality.

Note High concern reflects serious, potentially prolonged harm, supported by a RAD140 case report and FDA consumer safety determination. Oncology adverse-event rates are not healthy-user rates.

4/5
C
Cardiovascular caution6
Confidence: Medium

FDA warns that SARM-containing bodybuilding products may increase risk of heart attack or stroke.

Note This is a class/regulatory warning, not a quantified RAD140-specific consumer risk estimate.

3/5
C
Hormonal caution6
Confidence: Medium

FDA SARM warnings include sexual dysfunction, infertility, and testicular shrinkage. The incidence and reversibility of these outcomes specifically with RAD140 are not established.

Note Hormonal and endocrine effects are central to the compound identity, not incidental side effects.

3/5
C
Interaction risk3
Confidence: Low

Interactions and stacking safety are insufficiently characterized. Oncology-trial medication exclusions do not prove specific drug interactions.

Note Use trial exclusions as practical caution flags, not as a complete interaction list.

2/5
D
Pregnancy / lactation caution6
Confidence: High

FDA lists pregnancy miscarriage among SARM-associated concerns; lactation safety is unestablished. These are special-population cautions, separate from the overall adult risk assessment.

Note Avoid use in pregnancy or lactation contexts; do not present RAD140 as a supplement option.

4/5
C
Evidence uncertainty2
Confidence: High

Healthy-user efficacy, nootropic effects, consumer dosing, cycle design, and long-term safety remain unsupported or unclear in the public evidence checked.

Note Uncertainty is not itself quantified intrinsic harm and does not drive the overall risk escalation.

1/5
B
High caution8liver enzymes and bilirubin

A published case describes a previously healthy 24-year-old man with jaundice and liver injury after five weeks of oral RAD140 use. Improvement followed discontinuation, but recovery can be prolonged. Case reports cannot estimate incidence or prove product purity. Separately, the oncology trial reported frequent liver-test abnormalities at higher doses in heavily pretreated patients; those rates do not describe healthy consumers.

Risk context6

High risk reflects FDA warnings about serious harm from consumer SARM use, reinforced by RAD140 liver-injury reports in previously healthy adults. Moderate would understate the potential severity and prolonged recovery. Critical is not supported because the likelihood of catastrophic harm at any defined consumer dose is unknown. This is a qualitative assessment, not an incidence estimate; no typical safe oral dose or duration has been established. Pregnancy, medication interactions, and product contamination remain separate cautions.

08

Interactions and cautions

Trial exclusions3

The oncology protocol restricted several concurrent medicines and hormone-active agents. Such exclusions protect study interpretation and participants; they do not establish a validated interaction list. There is no reliable evidence that bodybuilding stacks or post-cycle regimens make RAD140 use safe.

10

Practical buying and quality notes

  • A label of 10 mg per capsule and 60 capsules implies 600 mg of labeled RAD140 per pack; that arithmetic does not confirm actual content or a safe dose. Compare pack price only after checking currency, pack count and ingredient amount. The two currently linked capsule records have inconsistent prices, so confirm the live retailer price before making a value comparison.9
  • A 2017 analysis of internet products marketed as SARMs found frequent identity and label-amount discrepancies. It did not test the current linked offers. A useful certificate of analysis (COA) should identify the matching batch, laboratory, substance and measured concentration; a generic purity claim does not establish clinical safety or legal status.9
11

FAQ

Is Testolone the same as RAD140?

1

Yes. Testolone is the common marketplace name for RAD140, and PubChem also lists vosilasarm among RAD140 synonyms. Product labels may use RAD140, RAD-140, Testolone, or vosilasarm, so identity testing matters.

What is the Testolone dosage?

2

There is no validated healthy-user dosage. The oncology doses described above are research context, not bodybuilding or nootropic guidance; a capsule label is not evidence of safety.

Does the half-life establish a cycle length?

2

No. Plasma half-life describes drug elimination, not useful effect duration, endocrine recovery, or a validated cycle. Healthy-user onset, duration and cycle timing remain unestablished.

Can athletes use RAD140?

7

RAD140 is prohibited at all times for athletes governed by WADA-based rules, according to USADA guidance checked on 14 October 2026. A research-use label does not remove that anti-doping restriction.

Is Testolone legal to buy?

6

Online availability is not legal approval. As of 14 October 2026, U.S. FDA states SARMs cannot legally be marketed as dietary supplements or drugs. Import, possession and product rules can differ elsewhere.

12

References

  1. PubChem Compound Summary for RAD140/Testolone/Vosilasarm, CID 44200882.
  2. LoRusso P, Hamilton E, Ma C, et al. A First-in-Human Phase 1 Study of a Novel Selective Androgen Receptor Modulator (SARM), RAD140, in ER+/HER2- Metastatic Breast Cancer. Clinical Breast Cancer. 2022;22(1):67-77.
  3. ClinicalTrials.gov record NCT03088527. Phase 1, First-in-Human Study of RAD140 in Postmenopausal Women With Breast Cancer.
  4. Miller CP, Shomali M, Lyttle CR, et al. Design, Synthesis, and Preclinical Characterization of the Selective Androgen Receptor Modulator (SARM) RAD140. ACS Medicinal Chemistry Letters. 2011;2(2):124-129.
  5. Yu Z, He S, Wang D, et al. Selective Androgen Receptor Modulator RAD140 Inhibits the Growth of Androgen/Estrogen Receptor-Positive Breast Cancer Models with a Distinct Mechanism of Action. Clinical Cancer Research. 2017;23(24):7608-7620.
  6. U.S. FDA. FDA Warns of Use of Selective Androgen Receptor Modulators (SARMs) Among Teens, Young Adults. Accessed 14 October 2026.
  7. U.S. Anti-Doping Agency. What Athletes Need to Know about Selective Androgen Receptor Modulators (SARMs).
  8. RAD-140 Drug-Induced Liver Injury. Ochsner Journal. 2022. PMID: 36561105.
  9. Van Wagoner RM et al. Chemical Composition and Labeling of Substances Marketed as Selective Androgen Receptor Modulators and Sold via the Internet. JAMA. 2017. PMID: 29183075.
Note

This page is informational and summarizes available evidence. It is not medical advice, a recommendation, or a substitute for guidance from a qualified clinician.