CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 19 enrolled
Drug / intervention
VGX-410 (Mifepristone) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00352911
NCT00352911Phase 2Completed

A Randomized, Placebo-controlled, Dose Escalating, Phase II Trial of the Anti -HIV-Activity and Safety of VGX-410 (Mifepristone) in HIV-1 Infected Subjects

VGX Pharmaceuticals, LLC·interventional·Posted Jul 17, 2006·Updated Mar 9, 2010

In Brief

A Phase 2 clinical trial evaluating VGX-410 (Mifepristone) and Placebo for VGX-410 (Mifepristone) for HIV Infections. Completed, enrolled 19 participants across 3 sites.

Detailed Summary

The objective of the study is to determine whether mifepristone (VGX-410) has anti-HIV-1 activity at doses of either 300 mg or 600 mg per day after oral administration for 14 days at each dose level.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHIV Infections
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 17, 2006
Enrollment StartJul 1, 2006
Primary CompletionJun 1, 2007
Study CompletionNov 1, 2007
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 20.0 years ago

Interventions

VGX-410 (Mifepristone)drug

Placebo for VGX-410 (Mifepristone)drug