A Safety and Pharmacokinetic Study of Proellex®

Phase 1

Completed

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

Detailed Description: This is an open-label, single-center, outpatient, unblinded, multi-dose study of the safety and pharmacokinetic properties of Proellex®. Six female subjects will each receive seven daily doses of Proellex® in separate, rising doses. Dosing must be accomplished between menstrual periods. The first six women will complete the 100 mg visit schedule before the next six women will begin the 150 mg visit schedule. Blood will be collected at pre-dose, and at 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 5, 8, 12, 24 and 36 (Day 7 only) hrs post-dose on Day 1 and Day 7. Subjects will be allowed to leave the clinic between the 12 and 24 hr and the 24 and 36 hr PK blood draws. Subjects will be discharged from the study after a one month follow-up visit. Safety will be assessed throughout the study.

Recruitment & Eligibility

Inclusion Criteria

Subject must be able to speak, read and understand English and be willing and able to provide written informed consent on an Institutional Review Board (IRB)-approved form prior to the initiation of any study procedures. Subject must have signed and dated a written Informed Consent Form (ICF) before undergoing any study related activities, including discontinuation of any prohibited medications
Premenopausal women aged 18 - 34 inclusive with body mass index between 18 and 35 inclusive
Women of child-bearing potential must be willing to use effective non-hormonal, double-barrier method contraception during the study period and for a minimum of 30 days after discontinuation of the study medication. Women who have had a hysterectomy will be allowed into the study
Must have a negative urine pregnancy test at screening
Able to swallow gelatin capsules
In general good health
Must have agreed to not attempt to become pregnant at any time during study participation or for 30 days thereafter
Must not have used tobacco (nicotine products) for at least two years before the study starts
Must have normal (or abnormal and clinically insignificant) laboratory values at screening
Willing to remain in the clinic for the screening visit and for the treatment visits
Available for all treatment and follow-up visits
Willing to comply with all study procedures
Additional inclusion criteria may apply

Exclusion Criteria

Pregnant or lactating females or women who are attempting or expecting to become pregnant at any time during the study
Past or present history of experiencing any allergic reaction to the formulations administered in this study, or in the opinion of the Principal Investigator, suggests an increased potential for an adverse hypersensitivity
Any medical condition, which, in the judgment of the Principal Investigator, will prevent the subject from starting and/or completing the study
Past or present history of any significant cardiovascular, renal, hepatic disease, thrombophlebitis, thromboembolic disorders, or cerebrovascular accident requiring ongoing medical therapy or clinical intervention
A QTc interval of >450ms at screening
Subject with abnormal screening visit vital signs or clinical laboratory evaluation considered clinically significant by the Principal Investigator
Subjects with symptomatic uterine fibroids or endometriosis
Use of other oral contraceptives or hormonal treatments within 30 days of first dose of study medication
Use of a hormone-releasing intrauterine device
Subject with a history of alcohol and/or drug abuse
Known active infection of HIV, Hepatitis A, B or C
Subject who has participated in a clinical trial with investigational medication within 30 days prior to study medication administration or who plans to take an experimental drug prior to the end of 30 days after participation in this study

Arm && Interventions

Primary Outcome Measures

Name	Time	Method
Cmax Post Final Dose	7 days	To determine the safety and PK properties of 100 mg, 150 mg and 200 mg of Proellex® taken for seven days by healthy adult female subjects.
AUC Post Final Dose	7 days

Secondary Outcome Measures