Clinical Trials Directory

Trials / Completed

CompletedNCT01382069

Phase 1 Study of Dimethandrolone Undecanoate in Healthy Men

Single Dose, Dose-Ranging and 28-Day Repeat-Dose Safety and Tolerability, Pharmacokinetics, and Pharmacodynamics Study of Dimethandrolone Undecanoate (DMAU) in Healthy Men

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center · Academic / Other
Sex
Male
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The long term objective is to develop a new male hormone Dimethandrolone Undecanoate (DMAU) as a male hormonal contraceptive. The study has two parts. The first is a dose escalating study in healthy to assess the safety and tolerability of single dose oral administration of DMAUin healthy men.(Completed) The second is to study the safety and tolerability of DMAU after 28 days of repeated daily dosing of DMAU in healthy men. (Currently Recruiting) In both parts the investigators will also study the pharmacokinetics of Dimethandrolone (DMA) in the serum after oral administration of DMAU.

Detailed description

The study will be conducted in two centers. 28-Day Repeat-Dose, Dose-Escalation Study: Based on the safety and tolerability of the single dose study and serum DMA levels attained, three doses of two formulations of DMAU were selected for a dose-escalating 28-day repeat dose study. Safety will be assessed in subjects receiving lower dosages before additional men receive higher doses for 28 days. Up to 100 men will be randomized to receive either active drug or an identical number of capsules of placebo. The 24-hour detailed PK of DMA will be assessed on day 1 and 28. Trough levels of DMA will be obtained throughout the 28-day period and at 48 and 72 hours after the last dose. In addition to safety and tolerability, suppression of serum T, gonadotropins, and SHBG will also be assessed as secondary pharmacodynamic (PD) endpoints. Psychosexual diaries for 7 consecutive days and PHQ-9 (questionnaire)will be obtained before and at the end of the study period.

Conditions

Interventions

TypeNameDescription
DRUGDimethandrolone UndecanoateDaily doses of 100, 200 and 400mg of dimethandrolone undecanoate
DRUGPlaceboPlacebo with capsules that look like the DMAU capsules but with no active ingredients

Timeline

Start date
2012-03-01
Primary completion
2017-02-01
Completion
2017-05-01
First posted
2011-06-27
Last updated
2025-11-20

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01382069. Inclusion in this directory is not an endorsement.