family=JetBrains+Mono:wght@400;500display=swap" as="style" onload="this.onload=null;this.rel='stylesheet'">
Research & Educational Use Only. RAD-140 is an investigational compound not approved by the FDA. It is banned by WADA and most athletic organizations. Not medical advice. Consult a healthcare professional.
SARM (Selective Androgen Receptor Modulator)Evidence Grade: B- (Phase 1 Human, Preclinical)Hormonal Suppression — PCT Required

RAD-140 (Testolone) Protocol Guide

RAD-140 (Testolone) is a non-steroidal selective androgen receptor modulator (SARM) developed by Radius Health for potential treatment of breast cancer and muscle wasting. It selectively binds androgen receptors in muscle and bone with an anabolic-to-androgenic ratio of approximately 90:1, meaning potent anabolic effects with reduced prostate and hair follicle androgenic activity. RAD-140 also demonstrates neuroprotective properties via AR-dependent pathways. This protocol covers 10-20mg daily oral dosing for 8-12 weeks, mandatory PCT, liver and hormonal monitoring, and harm reduction strategies.

Protocol Overview

Compound
RAD-140 (Testolone)
Category
Non-Steroidal SARM
Mechanism
Selective androgen receptor agonist in muscle/bone; tissue-selective activation; AR-mediated neuroprotection; partial agonist in prostate
MW
393.8 Da
Half-Life
~60 hours
Form
Oral solution or capsule
Route
Oral
Frequency
Once daily
Cycle
8-12 weeks + 4-week PCT

Dosing

PhaseWeeksDoseNotes
Introduction1-210 mg/dayAssess tolerance; take with food AM
Standard3-815-20 mg/dayOnce daily, same time each day
Extended (advanced)9-1210-20 mg/dayOnly if bloods remain acceptable
PCTPost-cycle 1-4Enclomiphene 12.5-25mg or Nolvadex 20/10mgBegin 3-5 days after last dose

Do not exceed 12 weeks. The long half-life (~60 hours) means steady-state is reached within ~2 weeks. Liver support (NAC 600mg + TUDCA 250mg daily) is recommended throughout the cycle.

Timeline

Week 1-2
Increased aggression in training. Mild strength improvements. Enhanced vascularity. Slight water retention possible.
Week 3-6
Significant strength gains (+10-20% on compound lifts). Lean mass accrual (3-6 lbs). Improved recovery. Enhanced muscle fullness and vascularity. Testosterone suppression begins.
Week 7-12
Peak lean mass and strength gains. Body recomposition (simultaneous fat loss and muscle gain). Suppression of endogenous testosterone may become more pronounced. Some users report mild lethargy.

Side Effects & Stacking

Side Effects

  • Testosterone suppression (dose and duration dependent)
  • Elevated liver enzymes (ALT/AST) — monitor closely
  • HDL cholesterol reduction (lipid impact)
  • Mild aggression/irritability
  • Hair shedding (rare, usually reversible)
  • Mild insomnia at higher doses
  • Lethargy toward end of cycle (suppression sign)

Stacking

  • MK-677: GH axis support + appetite (popular combination)
  • GW-501516 (Cardarine): Endurance + fat oxidation (research only)
  • BPC-157: Joint/tendon support during heavy training
  • NAC + TUDCA: Liver protection (essential, not optional)
  • Do NOT stack with: other SARMs, oral steroids, or prohormones

Blood Work

PanelMarkersTiming
HormonalTotal/free testosterone, LH, FSH, SHBG, estradiolBaseline, Week 6, post-PCT Week 4
LiverALT, AST, GGT, bilirubinBaseline, Week 4, Week 8
LipidsTotal cholesterol, HDL, LDL, triglyceridesBaseline, Week 8
BasicCBC, CMP, PSA (males over 40)Baseline, Week 8

Critical: If ALT/AST exceed 3x upper limit of normal, discontinue immediately. If total testosterone drops below 200 ng/dL mid-cycle with significant symptoms, consider early cycle termination and PCT. Post-PCT blood work is mandatory to confirm HPTA recovery.

Related Resources

Follistatin 344 Protocol IGF-1 LR3 Protocol PEG-MGF Protocol Dosing Calculator Reconstitution Calculator Bloodwork Planner Stack Checker Peptide Catalog
★ OFFICIAL SPONSOR
BioRoot AI
Free Functional Assessment
AI-powered root cause analysis & care plan
Start Free
Paid partnership · Learn more
Share & Save
𝕏 Share on Twitter 📱 Share on Reddit 💬 WhatsApp ✉️ Email 🔗 Copy Link 🖨️ Print / Save PDF Save to Favorites