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Completed Phase 2 Interventional

MGCD290 and Fluconazole Versus Fluconazole Alone for the Treatment of Moderate to Severe Vulvovaginal Candidiasis

ClinicalTrials.gov ID: NCT01497223

Public ClinicalTrials.gov record NCT01497223. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 7:06 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled Phase II Study of Fluconazole Versus Fluconazole And MGCD290 for the Treatment of Moderate to Severe Vulvovaginal Candidiasis

Study identification

NCT ID
NCT01497223
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MethylGene Inc.
Industry
Enrollment
220 participants

Conditions and interventions

Interventions

  • MGCD290 Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2011
Primary completion
Mar 31, 2013
Completion
Mar 31, 2013
Last update posted
Apr 3, 2013

2011 – 2013

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Women's Health Care Research Corp. San Diego California 92123
Altus Research Lake Worth Florida 33461
Healthcare Clinical Data, Inc. North Miami Florida 33161
Georgia Health Sciences University Augusta Georgia 30912-3500
Clinical Trials Management Covington Louisiana 70433
Clinical Trials Management, LLC Metairie Louisiana 70006
Harper University Hospital Detroit Michigan 48201
Clinical Research of Nevada Las Vegas Nevada 89123
SUNY Downstate Medical Center Brooklyn New York 11203
Lyndhurst Clinical Research Raleigh North Carolina 27607
Lyndhurst Clinical Research Winston-Salem North Carolina 27103
Drexel University College of Medicine Philadelphia Pennsylvania 19102
Magee-Womens Hospital of UPMC Pittsburgh Pennsylvania 15213
Medical University of South Carolina Charleston South Carolina 29403
Brownstone Clinical Trials Irving Texas 75061
Physician's Research Options Sandy City Utah 84070
Tidewater Physicians for Women Norfolk Virginia 23502
University of Washington Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01497223, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 3, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01497223 live on ClinicalTrials.gov.

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