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NCT02274181 · ClinicalTrials.gov registry record · Phase 1

An Open-Label, Single-Dose Study to Assess the Absorption, Metabolism, Excretion, and Mass Balance of Radiolabeled Androxal in Healthy Male Subjects After Oral Administration

A Phase 1 study, sponsored by Repros Therapeutics.

Completed
Registry status
Phase 1
Development phase
6
Enrollment target

NCT02274181 is a Phase 1 study that has completed, run by Repros Therapeutics. The registered enrollment target is 6 participants.

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The verdict

NCT02274181, a Phase 1 study, has completed, sponsored by Repros Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

The purpose of this study is to investigate the route(s) of elimination and mass balance of enclomiphene after oral administration of a single 25 mg (approximately equivalent to \[(\~\]) 500 nanocurie \[nCi\]) dose of \[14C\]Androxal in healthy adult male subjects.

Interventions

  • DRUG Androxal

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2014-12
Est. Completion 2015-01
Phase Phase 1

Sponsor

Repros Therapeutics

50 total trials

What the Registry Record Tells You About NCT02274181

The ClinicalTrials.gov registry entry for NCT02274181 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. The listed sponsor is Repros Therapeutics, which has 50 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Androxal is the first listed.

NCT02274181 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02274181 about?

NCT02274181 is a clinical study titled "An Open-Label, Single-Dose Study to Assess the Absorption, Metabolism, Excretion, and Mass Balance of Radiolabeled Androxal in Healthy Male Subjects After Oral Administration". The purpose of this study is to investigate the route(s) of elimination and mass balance of enclomiphene after oral administration of a single 25 mg (approximately equivalent to \[(\~\]) 500 nanocurie \[nCi\]) dose of \[14C\]Androxal in healthy adult male subjects.

What is the current status of trial NCT02274181?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2014-12. Estimated completion is 2015-01.

What interventions are being tested in trial NCT02274181?

The interventions under investigation include: Androxal (DRUG).

Who is sponsoring clinical trial NCT02274181?

This trial is sponsored by Repros Therapeutics, which has 50 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.