SARM Review Tables
Study Title | ClinicalTrials.gov Identifier | Phase | Design | Intervention | Patient Population | Primary outcome | Status |
---|---|---|---|---|---|---|---|
Pembrolizumab and Enobosarm in Treating Patients with Androgen Receptor Positive Metastatic Triple Negative Breast Cancer | NCT02971761 | Phase 2 | Intervention model: single group assignment | Enobosarm + Pembrolizumab | Patients with metastatic triple negative breast cancer | Safety and tolerability of treatment, response rate | Recruiting; estimated primary completion June 2018 |
Study to Assess Enobosarm (GTx-024) in Postmenopausal women with Stress Urinary Incontinence (ASTRID) | NCT03241342 | Phase 2 | Randomized placebo controlled | Enobosarm vs placebo | Postmenopausal women aged 18–80 with stress urinary incontinence | Change in number of stress urinary incontinence episodes | Not yet recruiting |
A Selective Androgen Receptor Modulator For Symptom Management in Prostate Cancer | NCT02499497 | Phase 2 | Randomized placebo controlled trial | LY2452473 vs placebo | Men who have undergone prostatectomy for prostate cancer | Harbor-UCLA 7-day Sexual Function Questionnaire | Recruiting; estimated primary completion March 2019 |
Safety, Tolerability, Pharmacokinetic (PK), and Pharmacodynamic Study of GSK 2881078 and Study to Evaluate he Effect of CYP3A4 Inhibition on PK of GSK2881078 | NCT02567773 | Phase 1 | Randomized placebo controlled trial | Part A: GSK2881078 Vs Placebo Part B: GSK2881078 + Itraconazole | Part A: Healthy men aged 50–75, postmenopausal women Part B: Healthy men aged 18–60 | Measures of tolerability and AEs, pharmacokinetic and pharmacoynamic measurements | Completed |
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Study of GSK2881078 in Single and Repeat Doses | NCT 02045940 | Phase 1 | Randomized placebo controlled crossover assignment | GSK2881078 vs placebo | Healthy males aged 18–50 | Safety and tolerability, pharmacokinetics, pharmacodynamics | Completed |
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of GSK2849466 in Healthy Male Subjects | NCT01696604 | Phase 1 | Randomized placebo controlled crossover assignment | GSK2849466 vs placebo | Healthy males aged 18–50 | Safety and tolerability, pharmacokinetics, pharmacodynamics | Completed |
Study to Evaluate Safety and Tolerability of Single and Multiple Ascending Doses of PF – 06260414 in Healthy Western and Japanese Male Subjects | NCT02070939 | Phase 1 | Randomized placebo controlled | PF-06260414 vs placebo | Healthy males aged 21–50 | Safety and tolerability, pharmacokinetics, pharmacodynamics | Completed |
GLPG0492 Pharmacodynamics | NCT01538420 | Phase 1 | Randomized placebo controlled | GLPG0492 vs placebo | Healthy males aged 18–50, post-menopausal women aged 35–65 | Safety and tolerability, pharmacokinetics, pharmacodynamics, effect on protein synthesis in muscle | Completed |