RAD-140 (testolone) is an experimental, nonsteroidal SARM whose official drug name is now vosilasarm. Its only published human trial tested it as a breast cancer drug in 22 women, where liver-enzyme rises were the most common side effect; no study has measured muscle, strength or body fat in people (LoRusso 2022). It is not approved anywhere, and WADA bans it in sport at all times (WADA 2026).

Below: every RAD-140 study we found, what they show about muscle, side effects and testosterone, the doses studies used, its legal status, and links to all of our RAD-140 guides.

What is RAD-140 (testolone)?

RAD-140 is a selective androgen receptor modulator: a drug that binds the same androgen receptor as testosterone but was designed to act more on muscle and bone than on tissues such as the prostate. It was first described in 2011 (Miller 2011) and comes from Radius Health, whose SARM patent covers it (US patent 8,629,167). The same molecule goes by several names: RAD140, testolone, vosilasarm and the trial code EP0062 (PubChem CID 44200882). UK Anti-Doping also lists “Radarine” as a name it is sold under (UK Anti-Doping).

Chemical structure of RAD-140 (testolone, vosilasarm)
RAD-140 is nonsteroidal: its structure is not built on the steroid ring system of testosterone.

In rats, a muscle used to test androgens (the levator ani) responded from 0.03 mg/kg, with less effect on the prostate (Miller 2011). That kind of tissue selectivity is what made SARMs interesting, but a 2026 review notes that it is reproducible in animals and small in humans, and that no SARM has been approved in more than 25 years (Adolf 2026). RAD-140’s developer path today is cancer, not muscle: Ellipses Pharma is testing it as EP0062 in a Phase 1/2 trial in advanced breast cancer (Ellipses Pharma 2024; NCT05573126).

RAD-140 research at a glance

Human studies come first. Animal and cell results are labeled as such: they show what a drug can do in a model, not what it does in people.

Study Who Dose and length What it found Evidence
Phase 1 trial (LoRusso 2022) 22 postmenopausal women with ER+/HER2- metastatic breast cancer 50, 100 or 150 mg/day until the cancer progressed (median 2.3 months) Highest tolerated dose 100 mg/day. AST rose in 59% and ALT in 45%; serious (grade 3/4) rises in 23%. One partial tumor response. SHBG fell in all 18 patients measured. Half-life about 45 hours. Muscle not measured. Human trial
EP0062 (vosilasarm) Phase 1/2 (NCT05573126) Advanced AR+/HER2-/ER+ breast cancer Recruiting No results yet. Human trial (ongoing)
Micro-dose excretion studies (Wagener 2022) Six studies, 5 healthy men each 1, 10 or 50 µg, once or for 5 days After a single 50 µg dose, RAD-140 was found in urine for up to 29 days. No effects on the body were measured. Anti-doping study
Miller 2011 Rats; young male monkeys (3 per group) Rats from 0.03 mg/kg; monkeys 0.1 mg/kg/day for 28 days Rat muscle grew with less effect on the prostate. Monkeys gained more than 10% body weight; the lean-mass change on DEXA was not quite significant. Testosterone fell by about two-thirds. Animal
Puskas 2025 Young male rats 14 days Larger muscle fibers than untreated rats, but no added effect on top of muscle overload; bone structure unchanged. Animal
Brown 2023 Young and adult female mice 5 mg/kg for 10 weeks Higher frailty and mortality risk; no strength gain. Animal
Yu 2017 Mice with human breast tumor grafts Not applicable Slowed the growth of AR/ER-positive tumors. Animal

See how RAD-140’s research stage compares with other compounds in the SARMs database.

Does RAD-140 build muscle? What the evidence shows

Muscle and strength in people: never tested

No human trial has measured muscle, strength or body composition with RAD-140. The completed Phase 1 trial was a cancer study (NCT03088527), and the anti-doping studies only measured urine levels (Wagener 2022). Every claim about RAD-140 and muscle in people therefore rests on user reports, not measurements.

Muscle in animals: mostly positive, one negative study

In rats, RAD-140 increased the weight of the levator ani muscle, and in young male monkeys 28 days raised body weight by more than 10% (Miller 2011). A 2025 rat study found larger muscle fibers after 14 days (Puskas 2025). The one study in female mice went the other way: 10 weeks raised frailty and mortality risk and did not improve strength (Brown 2023).

Fat loss: not established

No human study has measured body fat with RAD-140. The weight loss and low appetite seen in about a quarter of Phase 1 patients occurred in people with advanced cancer and are listed there as side effects (LoRusso 2022).

RAD-140 results and before-and-after reports

Because no study has measured results in healthy people, before-and-after photos cannot separate RAD-140’s effect from training, diet, other drugs or a mislabeled product. For comparison, SARMs that were tested in randomized trials added roughly 1 to 1.5 kg of lean mass (Adolf 2026). Our RAD-140 before and after page collects user reports next to that context, and the older 8-week RAD-140 log is one user’s account. For timing questions, see when do SARMs kick in.

RAD-140 side effects

The table lists what has been documented, from the strongest evidence to the weakest. Case reports describe single patients, often using several products, so they cannot prove that RAD-140 alone caused the problem.

Side effect What was found Evidence
Raised liver enzymes and bilirubin AST rose in 59.1%, ALT in 45.5% and bilirubin in 27.3% of Phase 1 patients; grade 3/4 AST/ALT rises in 22.7% (LoRusso 2022). Trial
Vomiting, dehydration, low appetite, weight loss Each in 27.3% of Phase 1 patients; grade 3/4 low phosphate in 22.7%. These patients had advanced cancer (LoRusso 2022). Trial
Cholestatic liver injury and jaundice Reported after weeks to months of RAD-140 products, usually improving after stopping (Barbara 2020; Leung 2022; Ladna 2023; Perananthan 2024; Demangone 2024; Niazi 2025). In a 2026 case (the product also contained andarine), the patient needed corticosteroids, plasmapheresis and intensive care (Dao 2026). Case reports
Myocarditis and myopericarditis Heart-muscle inflammation in a young man (Padappayil 2022) and in a 16-year-old boy after his first dose (Schwartzman 2024). Case reports
Heart failure Described in a man who used RAD-140 (Skorupski 2024). Case report
Breast growth and low testosterone After supplements containing RAD-140, MK-677 and cardarine plus undeclared hormones; it resolved after stopping (Chong 2024). Case report
Spleen rupture In a man using RAD-140 with MK-677; the authors call any link speculative (Jaffry 2026). Case report
Lower testosterone Fell by about two-thirds in young male monkeys in 28 days; not measured in men (Miller 2011). Animal

The FDA says life-threatening reactions, including liver injuries that needed hospital care, have occurred in people taking SARM products (FDA). For every side effect across all SARMs, see SARMs side effects and are SARMs liver toxic?

RAD-140 with MK-677

Several of the case reports above involved MK-677 (ibutamoren) as well: the breast-growth case (Chong 2024) and the spleen rupture (Jaffry 2026). A 47-year-old bodybuilder who took RAD-140, andarine and ibutamoren for 3 months developed blood sugar of 558 mg/dL and needed insulin; his doctors thought ibutamoren played the main role (Sotorník 2022). MK-677’s own risks are covered in MK-677 side effects, and the combination in MK-677 and RAD-140 stack.

Gyno, hair loss, acne and blood pressure

No study has looked at hair loss, acne or blood pressure with RAD-140, and the case reports in our sources do not describe them. The one breast-growth case involved undeclared hormones (Chong 2024). What is known about each across SARMs: RAD-140 gyno, do SARMs cause gyno?, SARMs and hair loss, SARMs and acne, SARMs and blood pressure and SARMs and alcohol.

Does RAD-140 suppress testosterone?

Probably, although no trial has measured it in men. In young male monkeys, 28 days of RAD-140 lowered testosterone from about 600–800 to about 200–300 ng/dL (Miller 2011). In the human trial, SHBG fell in every patient measured, a sign that the drug was acting on androgen receptors (LoRusso 2022). Case reports describe low testosterone in men whose products contained RAD-140 together with other drugs (Chong 2024).

How fast hormones recover after RAD-140 has not been studied. With LGD-4033, another SARM, testosterone and SHBG were back to baseline about 5 weeks after a 21-day trial ended (Basaria 2013). After longer cycles of anabolic steroids, testosterone recovered within 3 months in most men, but sperm counts took about a year and 11% still had low testosterone at the end of follow-up (Smit 2021).

Testosterone suppression: RAD-140 compared Sarmguide score from 0 (none found) to 3 (marked suppression), based on the cited studies of each compound. "(animal)" means the score rests on animal data because suppression was not measured in men; compounds with no data at all are left out. RAD-140: No trial has measured testosterone in men taking RAD-140. In young male monkeys, 28 days lowered testosterone by roughly two-thirds. In the human Phase 1 trial (women), SHBG fell in every patient measured, a sign of androgen-receptor activity. Case reports in men describe low testosterone after products that contained RAD-140 together with other drugs.
Testosterone suppression: RAD-140 comparedLGD-4033: Marked; RAD-140: Moderate (animal); AC-262: Moderate (animal); Andarine (S4): Moderate (animal); Ostarine: Moderate; S-23: Moderate (animal); MK-677: Mild; Anastrozole: None found; Clomiphene: None found; Enclomiphene: None foundNone foundMildModerateMarkedLGD-4033LGD-4033: MarkedMarkedRAD-140RAD-140: Moderate (animal)Moderate (anim…AC-262AC-262: Moderate (animal)Moderate (anim…Andarine (S4)Andarine (S4): Moderate (animal)Moderate (anim…OstarineOstarine: ModerateModerateS-23S-23: Moderate (animal)Moderate (anim…MK-677MK-677: MildMildAnastrozoleAnastrozole: None foundNone foundClomipheneClomiphene: None foundNone foundEnclomipheneEnclomiphene: None foundNone found

Source: Sarmguide compound database; RAD-140: Design, Synthesis, and Preclinical Characterization of the Selective Androgen Receptor Modulator (SARM) RAD140 (2011).

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More detail: RAD-140 suppression, RAD-140 PCT, PCT after SARMs, do SARMs lower testosterone? and do SARMs shrink your balls? The PCT and bloodwork planner lists the tests and the PCT drugs that have been studied.

Bloodwork: the markers that changed in studies

Liver enzymes, bilirubin and SHBG changed in the RAD-140 trial. Testosterone, FSH, SHBG and HDL cholesterol are the markers that changed in trials of other SARMs (Basaria 2013). These are the tests that track those changes:

  • ALT and AST (liver enzymes) and bilirubin
  • Total and free testosterone, LH and FSH
  • SHBG
  • Lipid panel (HDL and LDL cholesterol)

What each test means and when it is usually taken: SARMs bloodwork guide and low testosterone blood test.

RAD-140 dosage: what studies used

The only human treatment doses on record are from the Phase 1 trial: 50, 100 or 150 mg a day in women with advanced breast cancer, where 100 mg/day was the highest dose tolerated (LoRusso 2022). No study has tested any dose of RAD-140 for muscle or performance in healthy people, so there is no evidence-based “muscle dose”. The anti-doping studies used micro-doses of 1 to 50 µg to study detection, not effects (Wagener 2022).

Products are sold by label strength. SwissChems, for example, sells RAD-140 as 10 mg capsules. For liquids, how many mL a dose is depends entirely on the concentration printed on the bottle (mg per mL); no study has tested liquid RAD-140. Our RAD-140 dosage guide sets trial doses next to what users report, and liquid SARMs covers liquids, pills and powders.

RAD-140 half-life

About 45 hours (44.7 h), measured in the Phase 1 trial at 50–150 mg/day (LoRusso 2022). It is the only human pharmacokinetic figure published, and it may differ in men or at lower doses. At that half-life, roughly 70% of a dose is still in the body 24 hours later, which is why the question of morning or night matters less for RAD-140 than for short-acting drugs; no study has compared dosing times.

  • United States: not FDA-approved. The FDA says products containing SARMs are illegally marketed, unapproved drugs, not dietary supplements (FDA). SARMs are not federally scheduled: a 2019 bill to schedule them was introduced and sent to committee, and GovInfo holds no later version (GovInfo).
  • United Kingdom: UK Anti-Doping lists vosilasarm (RAD-140, Radarine, testolone) among SARMs, says no SARM is approved for human use anywhere, and notes that the Food Standards Agency treats SARMs as unauthorized novel foods, so they are illegal to sell or advertise as food or in supplements (UK Anti-Doping).
  • Australia: SARMs are prescription-only (Schedule 4) and listed in Appendix D clause 5, so possession without authority such as a prescription is illegal (Poisons Standard 2026).
  • Germany: the annex to the Anti-Doping Act names “RAD-140, synonym Testolon” (AntiDopG annex). The Act bans trading in listed substances for doping in sport and acquiring or possessing a “non-small quantity” for doping in sport (AntiDopG §2).
  • Prescription or pharmacy: RAD-140 is not an approved medicine in any country we could find (LoRusso 2022), so there is no prescription or pharmacy version anywhere.

Country by country: are SARMs legal?, SARMs in Europe and SARMs in Australia.

RAD-140 in sport and drug tests

WADA lists RAD140 by name under S1.2 (other anabolic agents) and prohibits it at all times (WADA 2026). Testing is very sensitive: a single 50 µg micro-dose was found in urine for up to 29 days (Wagener 2022), and 50 µg rubbed on the forearm was detected for up to 9 days (Korsmeier 2025). RAD-140 was one of the three SARMs most often found in a study of urine samples from men outside sport (Bohlin 2024). See SARMs and WADA, SARMs drug test and how long SARMs stay in your system.

RAD-140 vs other SARMs

Compound Human evidence Lean mass in trials Best-documented risks
RAD-140 One Phase 1 trial (women with breast cancer) Not measured Liver-enzyme rises in about half of trial patients; liver and heart case reports (LoRusso 2022)
LGD-4033 Two placebo-controlled trials +1.21 kg on 1 mg/day for 21 days (Basaria 2013) Testosterone, SHBG and HDL fell even at 1 mg; liver case reports
Ostarine Phase 2 and two Phase 3 trials +1.3 kg vs placebo on 3 mg/day for 86 days (Dalton 2011) HDL fell up to 27%; total testosterone fell; liver case reports
YK-11 None Not studied Case reports with other SARMs; FDA stroke report (FDA)
RAD-150 None Not studied Unknown: no published study (ClinicalTrials.gov)

Head-to-head pages: RAD-140 vs LGD-4033, ostarine vs RAD-140, YK-11 vs RAD-140 and RAD-140 vs RAD-150. Or put any two side by side with the compare tool.

RAD-140 stacks

No study has tested RAD-140 combined with another compound for muscle or fat loss. What exists are case reports of people who took combinations: cholestatic liver injury with RAD-140 plus LGD-4033 (Barbara 2020), breast growth and low testosterone with RAD-140, MK-677 and cardarine (Chong 2024), and diabetes-level blood sugar with RAD-140, andarine and ibutamoren (Sotorník 2022). Combining drugs that each affect the liver, hormones or blood sugar makes it harder to know which one caused a problem.

Our stack pages: RAD-140 stacks, RAD-140 and cardarine and MK-677 and RAD-140. The stack checker shows where the documented risks of any combination overlap.

Buying RAD-140: is it what the label says?

Often not, across the SARM market. When researchers bought 44 products sold online as SARMs, only 52% contained a SARM at all, 39% contained a different unapproved drug, 9% contained no active compound and 41% matched the amount on the label (Van Wagoner 2017). In almost all published SARM liver-injury cases, the product itself was never analyzed (Adolf 2026).

If you buy, look for a lot-specific certificate of analysis from an independent lab and learn how to read a lab test. Our current pick is SwissChems, which publishes lot-specific lab reports; the reasons and its weak points are in our SwissChems review, and where to buy SARMs explains what to check with any seller.

Bottom line

RAD-140 is a breast cancer drug candidate, not a tested muscle builder. Its one human trial found liver-enzyme rises in about half of patients, and liver injury is also the most common serious harm in case reports from people using it for muscle. The muscle data come from rats and three monkeys per group, and one mouse study was negative. It probably lowers testosterone, it is banned in sport and detectable for weeks, and it is illegal to sell as a supplement in the US, UK and Australia. Anyone weighing it up should know those facts first and keep an eye on liver and hormone blood tests with a doctor.

Charts

Doses used in human studies of RAD-140 What the published studies used and found. These are research doses reported in the studies, not recommendations. Dots mark each dose a study tested (per-kg doses are listed in the table only).
Dose studiedWho took partDurationWhat the study foundSource
50, 100 or 150 mg/dayPostmenopausal women with heavily pretreated ER+/HER2- metastatic breast cancer (n=22)Daily until disease progression (median progression-free survival 2.3 months)Open-label Phase 1 dose-escalation (3+3) with a pharmacokinetic expansion The maximum tolerated dose was 100 mg/day. AST rose in 59% and ALT in 45% of patients; serious (grade 3/4) AST/ALT rises occurred in 23%. One patient had a partial response. SHBG fell in all 18 patients measured.PubMed 2022

Sources: the studies linked in the table.

Half-life of RAD-140 compared Elimination half-life in people, where measured (log scale; bars show the reported range). Values from different studies and routes are not directly comparable.
Half-life of RAD-140 comparedTesamorelin: ~8–11 min; Ipamorelin: ~2 h; Enclomiphene: ~8–10 h; Ostarine: ~14–24 h; Clomiphene: ~5–24 h (No single value: enclomiphene part ~5–10 h; zuclomiphene part ~24 h with a very long tail (detectable for over a month)); LGD-4033: ~24–36 h (24–36 h); RAD-140: ~45 h; Anastrozole: ~2–2.1 days (~50 h); Tamoxifen: ~5–7 days (~5–7 days (tamoxifen); ~14 days (N-desmethyltamoxifen, main active metabolite)); CJC-1295: ~5.8–8.1 days (~6–8 days)6 min30 min1 h3 h6 h12 h1 day3 days1 weekTesamorelinTesamorelin: ~8–11 min~8–11 minIpamorelinIpamorelin: ~2 h~2 hEnclomipheneEnclomiphene: ~8–10 h~8–10 hOstarineOstarine: ~14–24 h~14–24 hClomipheneClomiphene: ~5–24 h (No single value: enclomiphene part ~5–10 h; zuclomiphene part ~24 h with a very long tail (detectable for over a month))~5–24 hLGD-4033LGD-4033: ~24–36 h (24–36 h)~24–36 hRAD-140RAD-140: ~45 h~45 hAnastrozoleAnastrozole: ~2–2.1 days (~50 h)~2–2.1 daysTamoxifenTamoxifen: ~5–7 days (~5–7 days (tamoxifen); ~14 days (N-desmethyltamoxifen, main active metabolite))~5–7 daysCJC-1295CJC-1295: ~5.8–8.1 days (~6–8 days)~5.8–8.1 days

Source: Sarmguide compound database; RAD-140 value: A First-in-Human Phase 1 Study of a Novel Selective Androgen Receptor Modulator (SARM), RAD140, in ER+/HER2- Metastatic Breast Cancer (2022).

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More on RAD-140

Frequently asked questions

What is RAD-140 (testolone)?

An unapproved experimental SARMEvidence: Law

RAD-140 is a nonsteroidal SARM first described in 2011; its official drug name is now vosilasarm, and it is being tested as EP0062 for breast cancer. It is not approved for any medical use.

Read the full section

What does RAD-140 do?

Activates the androgen receptorEvidence: Animal

In rats it increased muscle weight with less effect on the prostate, and in its one human trial, in women with breast cancer, SHBG fell in every patient measured. Its effect on muscle in people has never been tested.

Read the full section

Is RAD-140 a SARM or a steroid?

A SARM, not a steroidEvidence: Law

RAD-140 is nonsteroidal, meaning its structure is not a steroid, but it acts on the same androgen receptor. WADA lists it by name with the SARMs under S1.2.

Read the full section

Does RAD-140 build muscle in humans?

Never tested in humansEvidence: Animal

In rats it increased muscle weight and in young monkeys it raised body weight over 28 days, but a 2023 study in female mice found more frailty and no strength gain.

Read the full section

How long does RAD-140 take to kick in?

UnknownEvidence: Limited

No study has measured when any effect on muscle starts. In an anti-doping study, urine levels peaked 2 to 6 hours after a dose, and its half-life of about 45 hours means it stays in the body for days.

What is the half-life of RAD-140?

About 45 hoursEvidence: Trial

About 45 hours (44.7 h), measured in the Phase 1 trial in women with breast cancer taking 50–150 mg a day. No other human half-life has been published.

Read the full section

How many mL of RAD-140 per day?

No studied answerEvidence: Limited

No trial has tested RAD-140 for muscle in healthy people, and none has used a liquid; the only human treatment doses were 50, 100 and 150 mg a day in women with advanced breast cancer. For any liquid, the mL amount depends on the concentration on the bottle.

Read the full section

Is RAD-140 bad for the liver?

Its best-documented riskEvidence: Trial

In the Phase 1 trial, AST rose in 59% and ALT in 45% of patients. Many case reports describe jaundice and cholestatic liver injury in people using RAD-140 products, and some cases were severe.

Read the full section

Does RAD-140 suppress testosterone, and do you need PCT?

Probably; not measured in menEvidence: Animal

In young male monkeys, testosterone fell from about 600–800 to about 200–300 ng/dL in 28 days. How hormones recover after RAD-140 has not been studied.

Read the full section

Does RAD-140 cause gyno or hair loss?

Not studiedEvidence: Limited

One case report describes breast growth and low testosterone in a man whose supplements contained RAD-140, MK-677 and cardarine plus undeclared hormones; it resolved after stopping.

Read the full section

Is RAD-140 legal in Germany, the US and the UK?

Not approved anywhereEvidence: Law

Germany's Anti-Doping Act bans trading it or possessing a non-small quantity for doping in sport; the FDA says SARM products are unapproved drugs, not supplements. In the UK, SARMs cannot legally be sold or advertised as food or supplements.

Read the full section

Is RAD-140 banned in sport?

Yes, banned by WADAEvidence: Law

WADA names RAD140 on its Prohibited List and bans it at all times. In one study, a single 50 µg micro-dose was still found in urine 29 days later.

Read the full section

What is the difference between RAD-140 and RAD-150?

RAD-150 is an unstudied esterEvidence: Lab

PubChem lists RAD-150 (TLB-150) as a benzoate ester of RAD-140, and in a patent lab test it bound the androgen receptor about 65 times more weakly. RAD-140 has one small human trial; RAD-150 has no published studies at all.

Read the full section

Sources

  1. A First-in-Human Phase 1 Study of a Novel Selective Androgen Receptor Modulator (SARM), RAD140, in ER+/HER2- Metastatic Breast Cancer 2022 · PMID 34565686
  2. WADA: The Prohibited List (2026 List, in force from 1 January 2026) 2026
  3. Design, Synthesis, and Preclinical Characterization of the Selective Androgen Receptor Modulator (SARM) RAD140 2011 · PMID 24900290
  4. US Patent 8,629,167 B2: Selective androgen receptor modulators (Radius Health; granted 14 January 2014), Example 87 and Table 1 2014
  5. PubChem: RAD140 / Vosilasarm (CID 44200882), names and synonyms 2026
  6. SARMs | UK Anti-Doping (supplement ingredient warning, updated 29 April 2026) 2026
  7. Selective Androgen Receptor Modulators (SARMs) in Sport: Patterns of Use, Product Contamination, Health Risks and Doping-Control Implications 2026 · PMID 42919612
  8. Ellipses Pharma: Vosilasarm (EP0062), an oral Selective Androgen Receptor Modulator (SARM), poster presented at SABCS 2024 2024
  9. ClinicalTrials.gov NCT05573126: Phase 1/2 Study to Evaluate EP0062 as Monotherapy and in Combination in Patients With Advanced or Metastatic AR+/HER2-/ER+ Breast Cancer 2026
  10. Human In Vivo Metabolism and Elimination Behavior of Micro-Dosed Selective Androgen Receptor Modulator RAD140 for Doping Control Purposes 2022 · PMID 35888790
  11. ClinicalTrials.gov NCT03088527: Phase 1, First-in-Human Study of RAD140 in Postmenopausal Women With Breast Cancer 2020
  12. Preclinical assessment of the selective androgen receptor modulator RAD140 to increase muscle mass and bone mineral density 2025 · PMID 40680216
  13. RAD140 (Testolone) negatively impacts skeletal muscle adaptation, frailty status and mortality risk in female mice 2023 · PMID 37758180
  14. Drug-Induced Liver Injury Associated With Alpha Bolic (RAD-140) and Alpha Elite (RAD-140 and LGD-4033) 2020 · PMID 33062783
  15. RAD-140 Drug-Induced Liver Injury 2022 · PMID 36561105
  16. Idiosyncratic drug-induced liver injury related to use of novel selective androgen receptor modulator RAD140 (Testalone): a case report 2023 · PMID 36978171
  17. Severe liver injury following use of RAD-140, a selective androgen receptor modulator, for body building 2024 · PMID 38444893
  18. Selective Androgen Receptor Modulators Leading to Liver Injury: A Case Report 2024 · PMID 39328701
  19. Cholestatic Drug-Induced Liver Injury From Rad-140 Successfully Treated With Corticosteroids 2025 · PMID 40761329
  20. Unregulated gains: a case of RAD-140-induced liver injury 2026 · PMID 42417499
  21. Acute Myocarditis From the Use of Selective Androgen Receptor Modulator (SARM) RAD-140 (Testolone) 2022 · PMID 35233331
  22. Myopericarditis Following Use of Selective Androgen Receptor Modifier "RAD-140" 2024 · PMID 39157568
  23. Selective androgen receptor modulator abuse-induced heart failure: catastrophic effects of RAD-140 (Testolone) 2024 · PMID 38864168
  24. Reversible Gynecomastia and Hypogonadism Due to Usage of Commercial Performance-Enhancing Supplement Use 2024 · PMID 39145153
  25. Spontaneous Splenic Rupture in a Patient With Recent Use of Performance-Enhancing Compounds: A Case Report and Literature Review 2026 · PMID 42064485
  26. FDA: Certain bodybuilding products put consumers at risk for heart attack, stroke, serious liver damage and more (content current as of 2 December 2025) 2025
  27. Could Overt Diabetes Be Triggered by Abuse of Selective Androgen Receptor Modulators and Growth Hormone Secretagogues? A Case Report and Review of the Literature 2022 · PMID 35983415
  28. The safety, pharmacokinetics, and effects of LGD-4033, a novel nonsteroidal oral, selective androgen receptor modulator, in healthy young men 2013 · PMID 22459616
  29. Disruption and recovery of testicular function during and after androgen abuse: the HAARLEM study 2021 · PMID 33550376
  30. S. 2895 (IS) – Selective Androgen Receptor Modulators Control Act of 2019 (GovInfo)
  31. Therapeutic Goods (Poisons Standard—June 2026) Instrument 2026 (F2026L00633) 2026
  32. Anlage zum Anti-Doping-Gesetz (AntiDopG), Germany (BGBl. 2023 I Nr. 67) 2023
  33. § 2 Anti-Doping-Gesetz (AntiDopG): Unerlaubter Umgang mit Dopingmitteln (Germany)
  34. Exploring transdermal SARMs exposure: analysis of the elimination profiles and metabolism for doping control purposes 2025 · PMID 40632609
  35. Detection of anabolic agents including selective androgen receptor modulators in samples outside of sport 2024 · PMID 37986708
  36. The selective androgen receptor modulator GTx-024 (enobosarm) improves lean body mass and physical function in healthy elderly men and postmenopausal women: results of a double-blind, placebo-controlled phase II trial 2011 · PMID 22031847
  37. ClinicalTrials.gov search for 'RAD-150', 'RAD150' and 'TLB-150': no studies found (checked 30 October 2026) 2026
  38. Chemical Composition and Labeling of Substances Marketed as Selective Androgen Receptor Modulators and Sold via the Internet 2017 · PMID 29183075
  39. Selective Androgen Receptor Modulator RAD140 Inhibits the Growth of Androgen/Estrogen Receptor-Positive Breast Cancer Models with a Distinct Mechanism of Action 2017 · PMID 28974548
  40. PubChem: TLB 150 Benzoate (synonyms RAD150, RAD-150?), CID 68547459 2026