Pharmacokinetics, Safety and Efficacy Study of Proellex in Pre-menopausal Women With Symptomatic Uterine Fibroids
Clinical trial NCT00683917 · TERMINATED
Trial details
- NCT number
- NCT00683917
- Sponsor
- Repros Therapeutics Inc.
- Status
- TERMINATED
- Phase
- Phase 2
- Study type
- INTERVENTIONAL
- Start date
- 2008-05-01
- Primary completion
- 2009-08-01
- Enrollment
- 10
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