STUDresearch · Non-peptide
RAD-140
Also known as
Testolone · RAD140 · RAD 140 · Vosilasarm (INN / development naming) · EP0062 (reformulated clinical code) · Testalone (common misspelling in literature and forums) · Radius RAD140 (developer-adjacent search string)
Community talk. May be wrong. Not medical advice. Not a protocol. Not for human or animal use.
Systemic oral SARM — whole-body exposure with muscle/bone-biased AR agonism talk; not a local inject and not a peptide.
Amount increased in weeks 5–6 during a cut; subjective strength change, no bloodwork or assay.
Also 6.25 mg/day enclomiphene; ALT later reached 417 or higher and identity was questioned.
Twenty-two heavily pretreated postmenopausal metastatic-breast-cancer patients; not an athletic study.
Half-life & effect duration
- Half-life in the body
- Human studyAbout 44.7 hours
- Secondary clinical summariesAbout 45–60 hours
- Older vendor / forum estimateAbout 16–20 hours
- Felt duration people report
- Solo-use accountNo change for 2 weeks, strength changes in weeks 3–6, low drive after stopping
- Stacked-use accountFelt well for 4 weeks despite later marked liver-enzyme elevation
Tap a line to jump into the full notes. Research only — may be wrong.
Timing context & sources
Half-life in the body
The first-in-human oncology study reported a 44.7-hour RAD-140 half-life.
Twenty-two postmenopausal patients with heavily pretreated metastatic breast cancer received 50, 100 or 150 mg orally once daily; authors said 44.7 hours supported QD dosing.
Clinical formulation, oncology doses, disease state and population differ from unverified recreational products and users.
- LoRusso et al. — First-in-human Phase I RAD140 study (opens in a new tab)Twenty-two heavily pretreated postmenopausal metastatic-breast-cancer patients received 50, 100 or 150 mg orally QD; half-life was 44.7 hours.Oncology population/doses unlike gray-market use; no athletic benefit, recreational safety or product-equivalence inference.
Felt duration people report
Community reports do not establish a reproducible onset or felt-duration window.
One solo account described no change for two weeks, strength changes in weeks 3–6 and low drive after stopping; a stacked account felt well for four weeks before marked liver-enzyme elevation.
Anonymous reports, changing dose, training/diet, co-use and unverified identity prevent causal timing; laboratory injury may lack a distinctive felt warning.
- Reddit r/rad140 — RAD-140 cycle review, no PCT (opens in a new tab)No change for two weeks, then strength changes; 10 mg/day, 20 mg in week 5 and 25 mg later; after stopping, a few days better sleep then about a week of low drive/slower recovery.Anonymous uncontrolled eight-week account, no bloodwork/product assay; changing dose, cut and training confound attribution.
- Reddit r/SARMs — Bloodwork saved my ass (opens in a new tab)10 mg RAD-140 plus 6.25 mg enclomiphene daily; good mood/strength/pumps for four weeks, then ALT 417 and higher; updates reported falling ALT/AST after stopping.Anonymous stacked report; clinician reportedly questioned identity/purity, so exposure may have been mislabeled/adulterated.
- Perananthan and George — Severe liver injury following RAD-140 use (opens in a new tab)43-year-old reported online RAD-140 for two months, stopped one week before jaundice/pruritus; biopsy showed bland cholestasis; biochemistry normalized five months later.Single probable-ADR case based on online product without assay; not incidence.
Other context in this card
- FDA — Caution using SARMs in bodybuilding products (opens in a new tab)FDA states SARMs in bodybuilding products are unapproved drugs and associates them with serious concerns including liver injury.Class-level warning, not RAD-140-specific PK or incidence.
What people say
- Lean mass (community): Multi-week oral logs often claim several pounds of lean tissue with training/surplus; diet and prior training confounds are large. forum
- Strength: Faster progressive overload on compounds (bench/squat/dead) in the first 2–4 weeks is one of the most repeated claims. forum
- Dry / hard look: Later weeks — denser, more vascular appearance vs aromatizing AAS or “wetter” LGD is standard forum typology, not imaging-trial proof. forum
- Recomp: Fat loss with muscle hold on a deficit is frequently logged; calories and cardio usually co-credited. forum
- Vs ostarine (MK-2866): Cast as much stronger for size/strength; also more suppression and side talk. forum
- Vs LGD-4033: LGD = fuller/waterier mass; RAD = denser/drier strength look — popular pairing contrast, not a head-to-head RCT. forum
- Vs S-4 / YK-11 / S-23: Often ranked “strong but more usable” than YK/S-23 for first hard cycle; S-4 more cut/vision-side lore. forum
- Animals (anabolic): Oral RAD140 increased levator ani muscle weight with wide separation from prostate stimulation in castrate and intact rat models (Miller et al., ACS Med Chem Lett 2011). animal
- Animals (CNS): In cultured hippocampal neurons and kainate-lesioned rats, RAD140 matched testosterone’s neuroprotective signal on apoptotic/excitotoxic insults (Jayaraman et al., Endocrinology 2014) — research interest only, not a nootropic product claim. animal
- Clinic (not gym): Phase 1 breast-cancer AR-pathway work showed AR engagement (SHBG↓, PSA↑ in many patients) and limited antitumor signals — medical oncology, not physique outcomes. trial
- What is missing: No large placebo-controlled athletic lean-mass/strength trial at 5–30 mg/day recreational bands. trial
Doses people talk about
- Inspected oral reports plus broader band: One eight-week solo reviewer began at 10 mg/day, then described 20 mg/day in week 5 and 25 mg/day later; another author reported 10 mg/day with enclomiphene. These unverified products do not define a safe dose, and broader forum charts remain ~5–10 mg/day. forum
- Beginner oral band: ~5–10 mg once daily is the usual first-cycle discussion range; many first logs start at 10 mg. forum
- Intermediate band: ~10–20 mg/day for stronger lean-mass/strength aims in multi-week runs. forum
- Upper / advanced talk: ~20–30 mg/day in aggressive or second-cycle logs; side and suppression talk rises without proportional proof of better risk/benefit. forum
- Above 30 mg/day (recreational): Uncommon in careful write-ups; occasionally bragged; no community consensus that higher is smarter. forum
- Women (recreational talk): Sparse anecdotes at roughly ~5–10 mg/day with high virilization concern (voice, hair, clitoral changes); many forum voices steer women toward milder agents instead. forum
- Schedule: Once daily is default because of long clinical half-life; splitting AM/PM is minority practice and not required by PK. forum
- Capsule products: Fixed 5–10 mg capsules appear in stack logs; still unverified without third-party testing. forum
- Label risk: Gray-market mg on bottle ≠ verified pure RAD-140; adulteration with other SARMs/prohormones/steroids is a documented industry problem. forum
- Framing: Community-reported research-discussion ranges only — not advice, not prescriptions, not safety-validated protocols. forum
- Clinical oncology (not gym): First-in-human Phase 1 (LoRusso et al., Clin Breast Cancer 2022) tested roughly 50–150 mg/day oral in postmenopausal mBC; MTD/RDE ~100 mg once daily. trial
- EP0062 reformulation: Later vosilasarm (EP0062) dose-finding used lower absolute daily amounts (e.g. 10 mg BID selected as optimal Phase 2 dose in ASCO 2025 abstract of NCT05573126) — formulation/PK differ from classic RAD140 gym products. trial
How it may feel
- First 1–2 weeks conflict: One eight-week solo reviewer reported no change for two weeks; a separate 10 mg/day plus enclomiphene author described good mood, strength and pumps across four weeks before marked liver-enzyme elevation. forum
- Weeks 1–2: Strength and training “quality” comments often precede scale or mirror moves; pumps may feel denser. forum
- Weeks 3–4: Recomp/lean-mass anecdotes and first acne or hair-shed notes; common first bloodwork checkpoint in careful logs. forum
- Weeks 6–8: Peak strength/size claims on typical cycles; fatigue, libido drop, irritability, and lipid/liver anxiety also cluster here. forum
- Weeks 8–12: Longer bulk-style runs — more suppression, lipid crash, and “need PCT” talk; diminishing returns debated. forum
- On-cycle crash while still dosing: Some logs describe mid-cycle lethargy or flat libido when suppression outruns perceived anabolism. anecdote
- Post-cycle report: One solo reviewer described a few days of better sleep, then about a week of difficulty getting out of bed, lower motivation and slower recovery. No bloodwork was provided, so suppression was not established. anecdote
- Post-cycle months: Training-kept size varies widely; many attribute retention to diet/training more than the molecule. anecdote
Cycles people discuss
- Typical length: 6–8 weeks is the most common physique discussion window. forum
- Longer runs: 8–12 weeks for bulk-style aims; past ~12 weeks side/suppression talk dominates. forum
- Shorter intros: 4–6 week “test runs” appear when users are risk-averse or first-timing a strong SARM. forum
- Time off: Off-time ≥ on-time (plus recovery/PCT) is the usual forum rule of thumb — not a clinical standard. forum
- PCT default talk: SERMs after cycle — tamoxifen (Nolvadex) and/or clomiphene (Clomid) language for several weeks is near-default in RAD threads. forum
- PCT timing debate: With ~45–60 h clinical half-life, some wait ~5–14 days after last dose before SERMs; older 16–20 h guides said sooner — both patterns still circulate. forum
- Solo vs stack: Solo first cycle is common advice; dual SARMs or RAD+MK-677 = harder to attribute gains and usually more suppression/side load. forum
- Bloodwork culture: Pre, mid (~week 4–6), and post labs (total/free T, LH/FSH, lipids, AST/ALT, CBC) are repeatedly recommended in careful communities. forum
- Re-runs: After subjective recovery and/or labs in logs; multi-year repeated gray-market safety is not established. forum
- Bridge / cruise talk: Some advanced users discuss low-dose bridges or TRT-base + RAD — that is steroid-adjacent practice, not SARM-only “safe” lore. forum
- PCT folklore: AAS-board style PCT talk after RAD is common; evidence quality is forum-grade. forum
- Example PCT shapes (forum only): Nolvadex ~10–20 mg/day for ~4–6 weeks, or lower-dose Clomid, or short dual SERM runs; doses vary wildly and are not medical protocols. forum
Timing
- Forum conflict (legacy): Pre-Phase-1 guides widely claimed ~16–20 hour half-life; still copy-pasted on vendor blogs despite human PK. forum
- Practical dosing logic: Long clinical duration → once-daily oral is standard; split dosing is optional preference, not PK necessity. forum
- Steady state: Multi-day half-life implies levels build over roughly the first week+ of daily dosing. forum
- PCT / clearance talk: Longer half-life arguments push later SERM starts vs short-half-life AAS mental models. forum
- HPTA lag: Suppression of LH/FSH/T can outlast the last dose; recovery timelines in logs span weeks to months. forum
- Clinical half-life (primary): Phase 1 PK reported mean t½ ≈ 44.7 hours, supporting once-daily (QD) dosing (LoRusso et al., 2022). trial
- Reference range often cited: ~45–60 hour elimination half-life for vosilasarm/RAD140 in secondary clinical summaries. trial
- SHBG / PSA (clinic): Phase 1 oncology: SHBG fell in all measured patients (18/18); PSA rose in most (16/20) — target engagement markers, not gym benefits. trial
- Anti-doping: SARM metabolite detection windows can be long relative to last dose; tested athletes treat RAD as high-risk regardless of “oral only” framing. trial
More on what it is
- Why people care: Forums rank it among the strongest recreational oral SARMs for lean mass and strength vs ostarine, with a “drier” look narrative than LGD. forum
- Research lens: Vendor “Testolone” bottles are unregulated research chemicals; label mg ≠ verified identity or purity. forum
- Bro framing: Testolone — the “aggressive recomp SARM” people compare to a mild cycle, with suppression baggage. forum
- What it is: Investigational oral nonsteroidal SARM (RAD-140 / Testolone / vosilasarm); oxadiazole-aniline scaffold from Radius Health–line development. trial
- Mechanism talk: High-affinity AR agonist framed as tissue-selective (muscle/bone over prostate in animals); still suppresses the HPTA at common research-chem doses. animal
- Evidence: Preclinical muscle/neuro papers + Phase 1 in postmenopausal ER+/HER2− breast-cancer patients; no large athletic RCTs for physique outcomes. trial
- Clinical naming: Vosilasarm / EP0062 continues breast-cancer SARM programs at different formulations and doses than gray-market gym charts. trial
- Not: Not testosterone, not a 17α-alkylated oral steroid ester, not a peptide, not FDA-approved for bodybuilding, fat loss, or hypogonadism. trial
Stacks
- RAD + MK-677 (Ibutamoren): Classic “mass” stack — RAD anabolism + MK appetite/sleep/GH-axis narrative; water retention, fasting glucose, and hunger confounds are frequent. Community charts often pair ~10–20 mg RAD with ~10–25 mg MK daily. forum
- RAD + LGD-4033: Dual strong-SARM bulk; high suppression, lipid, and side-load talk; hard to know which agent drove gains. forum
- RAD + cardarine (GW-501516): Cutting/recomp + endurance/fat-oxidation narrative; GW is not a SARM and carries its own long-term safety debates. forum
- RAD + ostarine (MK-2866): “Potency + milder bridge” idea; attribution of results is murky; stacked suppression still expected. forum
- RAD + YK-11: Aggressive strength/myostatin-lore stack; side and suppression reputation is harsh in forums. forum
- RAD + S-4 (andarine): Recomp/cut aesthetics talk; S-4 vision-side lore adds separate risk. forum
- RAD as oral kickstart on TRT/blast: Some advanced AAS logs add RAD for dry strength — not a beginner SARM-only pattern. forum
- Liver support talk: TUDCA, NAC, milk thistle appear constantly next to oral SARM cycles — evidence of protection specifically for RAD is anecdotal. forum
- Lipid support talk: Fish oil, citrus bergamot, cardio, and diet changes discussed when HDL tanks on bloodwork. forum
- PCT adjuncts: SERMs as above; some add enclomiphene, hCG, or OTC “test boosters” — quality of evidence varies from prescription-drug lore to pure marketing. forum
- What stacks do not prove: Multi-compound logs cannot isolate RAD’s contribution; vendor “premade SARM stacks” often hide ratios and underdose. forum
Storage notes
- No mix instructions here: STUDresearch does not list reconstitution, diluent volumes, or syringe unit charts. People reconstitute many different ways and vial labels differ — that content creates more confusion than clarity. forum
- Storage (general talk only): Unopened research products are usually kept cool, dry, and away from light per the seller label. Anything after first use is product-specific — follow the label, not a universal forum SOP. forum
Watch for
- HPTA suppression: Meaningful LH/FSH/testosterone suppression is expected in community bloodwork at common 10–20 mg bands — low libido, fatigue, soft post-cycle gains, and “dead bedroom” complaints are frequent. forum
- “Non-methylated = safe liver” myth: Marketing claim that lack of 17α-alkylation makes RAD liver-safe is contradicted by clinical enzyme rises and bodybuilding DILI reports. forum
- Skin / hair: Acne and accelerated male-pattern shedding in susceptible users are standard side threads. forum
- Mood / CNS: Irritability, aggression (“RAD rage” lore), anxiety, or insomnia in a subset; others report flat mood when suppressed. anecdote
- Sexual function: On-cycle or post-cycle ED/libido crash tied to suppression; not fixed by “selectivity” marketing. forum
- Vision: True classic S-4 yellow-tint lore is less central to RAD, but any vision change still prompts stop-and-evaluate talk in stacks. forum
- Women-specific: Virilization risk (voice deepening, body/facial hair, menstrual disruption) even at low recreational mg — irreversible changes are a hard forum warning. forum
- Cardiac / BP: Less systematic data than lipids; some users report resting HR or BP anxiety; long-term CV risk of recreational SARM use is unknown. forum
- Not risk-free: Tissue-selective AR marketing ≠ absence of suppression, hepatotoxicity, lipid harm, or long-term unknowns. No approved recreational dose exists. forum
- Bloodwork culture: People who take it seriously check lipids, HCT, and hormones — shutdown stories are the cautionary genre. forum
- Unapproved-drug status: SARMs are not FDA-approved for human use and are not legal dietary-supplement ingredients. This card maps forum talk only — not a sourcing guide, not a safety claim, and not a promise of results. trial
- Animal suppression signal: In young male cynomolgus monkeys, 28-day oral RAD140 suppressed testosterone into a low-normal band across tested doses while still supporting body weight (Miller et al.) — selective muscle action ≠ no systemic endocrine effect. animal
- Liver — clinical oncology: Phase 1 mBC: elevated AST in ~59%, ALT ~46%, total bilirubin ~27% of patients; Grade 3 AST/ALT and hypophosphatemia among notable TEAEs (LoRusso et al., 2022). trial
- Liver — recreational case reports: Multiple published DILI cases (cholestatic or mixed pattern) after unsupervised RAD-140 or RAD+LGD products (e.g. Barbara et al. 2020 Alpha Bolic/Alpha Elite; Flores et al.; Leung et al. 2022 peak bilirubin extreme; Australian Prescriber severe injury case). Jaundice, pruritus, and high bilirubin weeks into use are documented. trial
- Lipids: Adverse HDL depression (and broader dyslipidemia talk) is common in bloodwork-sharing logs; monkey chemistry also showed large HDL drops at higher mg/kg. animal
- Source / product risk: Mislabeling, multi-SARM blends sold as pure RAD, prohormone/steroid adulteration, and wrong mg strength are documented industry problems (including named commercial “Alpha” products in DILI literature). trial
- Sport / law: WADA-prohibited anabolic agent class; not approved as a dietary supplement; research-chemical sales legality varies by jurisdiction; FDA has warned against SARMs in bodybuilding products. trial
- Evidence honesty: Physique outcome claims are almost entirely uncontrolled logs; strongest human safety PK/AE data are oncology Phase 1 at doses and populations unlike gym use. trial
