CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 25 enrolled
Drug / intervention
Proellexdrug
Likely dose
Proellex 25 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00619385
NCT00619385Phase 1Completed

A Safety and Pharmacokinetic Study of 100 mg, 150 mg and 200 mg of Proellex® Taken for Seven Days by Healthy Adult Female Subjects

Repros Therapeutics Inc.·interventional·Posted Feb 21, 2008·Updated Aug 8, 2014

In Brief

A Phase 1 clinical trial evaluating Proellex for Healthy. Completed, enrolled 25 participants across 1 site.

Detailed Summary

Dose escalating study of 7 daily doses of Proellex at 100 mg, 150 mg and 200 mg

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 21, 2008
Enrollment StartFeb 1, 2008
Primary CompletionSep 1, 2008
Study CompletionOct 1, 2008
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 18.4 years ago

Interventions

Proellexdrug

Proellex 25 mg capsules 100 mg, 150 mg or 200mg daily for 7 days