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Crossover Study of the Safety and PK Properties of Proellex®

Pharmacokinetics Clinical Trial

Official title:
A Phase I, Open-Label, Randomized, Single-Center, Unblinded, Single-Dose, Five-Way Crossover Study of the Safety and PK Properties of Proellex®

Clinical Trial Summary

Study to evaluate the PK of 25 mg and 50 mg of Proellex from 2 different suppliers in the fed and fasting states.

Clinical Trial Description

This study is intended to evaluate the pharmacokinetic properties of two doses (25 mg and 50 mg) of Proellex® formulated with microcrystalline cellulose (MCC) from 2 different suppliers in the fed and fasting states. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00749879
Study type Interventional
Source Repros Therapeutics Inc.
Contact
Status Completed
Phase Phase 1
Start date August 11, 2008
Completion date October 23, 2008
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