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NCT00881062 · ClinicalTrials.gov registry record · Phase 1
Investigate Absorption, Metabolism and Excretion of [14C}-Proellex Following Single Oral Dose in Healthy Females
A Phase 1 study of Metabolism and Absorption, sponsored by Repros Therapeutics.
- Completed
- Registry status
- Phase 1
- Development phase
- 6
- Enrollment target
- 1
- Study location
NCT00881062 is a Phase 1 study of Metabolism and Absorption that has completed, run by Repros Therapeutics. The registered enrollment target is 6 participants, below the 13,265-participant average among 19 other Metabolism trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00881062, a Phase 1 study of Metabolism and Absorption, has completed, sponsored by Repros Therapeutics.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 6 participants
- Enrollment target
- 1
- Study location
Study Summary
This study was to determine the ADME and metabolites of Proellex following a single oral dose of 25 mg.
Conditions Studied
Interventions
- DRUG Proellex
Study Locations (1)
Wisconsin
- Covance Clinical Research Unit Inc. - Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 6 participants |
| Start Date | 2009-04 |
| Est. Completion | 2009-06 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00881062
The ClinicalTrials.gov registry entry for NCT00881062 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 13,265-participant average among 19 other Metabolism trials with a reported enrollment target (100% lower). The listed sponsor is Repros Therapeutics, which has 50 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Metabolism appearing as the primary indexed condition, and to 1 intervention - of which Proellex is the first listed.
NCT00881062 reports 1 study location spanning 1 distinct geographic area - top geographies include Wisconsin.
Frequently Asked Questions
What is clinical trial NCT00881062 about?
NCT00881062 is a clinical study titled "Investigate Absorption, Metabolism and Excretion of [14C}-Proellex Following Single Oral Dose in Healthy Females". This study was to determine the ADME and metabolites of Proellex following a single oral dose of 25 mg.
What is the current status of trial NCT00881062?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2009-04. Estimated completion is 2009-06.
What conditions does trial NCT00881062 study?
This clinical trial studies the following conditions: Metabolism, Absorption, Excretion.
What interventions are being tested in trial NCT00881062?
The interventions under investigation include: Proellex (DRUG).
Who is sponsoring clinical trial NCT00881062?
This trial is sponsored by Repros Therapeutics, which has 50 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00881062 being conducted?
This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.