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Completed Phase 2 Interventional Results available

Dose-Finding Study of Oral Ibrexafungep (SCY-078) vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis

ClinicalTrials.gov ID: NCT03253094

Public ClinicalTrials.gov record NCT03253094. 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, 5:02 AM 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 Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral Ibrexafungerp (SCY-078) vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis

Study identification

NCT ID
NCT03253094
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Scynexis, Inc.
Industry
Enrollment
186 participants

Conditions and interventions

Interventions

  • Fluconazole Drug
  • SCY-078 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
Jul 31, 2017
Primary completion
May 3, 2018
Completion
May 3, 2018
Last update posted
Aug 11, 2021

2017 – 2018

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
UAB Personal Health Clinic Birmingham Alabama 35294
Precision Trials AZ, LLC Phoenix Arizona 85032
Women's Health Care Research Corp. San Diego California 92111
Gulf Coast Research Group, LLC Brandon Florida 33510
Altus Research, Inc. Lake Worth Florida 33461
OB-GYN Associates of Mid-Florida P.A. Leesburg Florida 34748
New Age Medical Research Corp. Miami Florida 33186
Visionary Investigators Network South Miami Florida 33160
Atlanta North Gynecology, P.C. Roswell Georgia 30075
Cypress Medical Research Center, LLC Wichita Kansas 67226
Clinical Trials Management, LLC Covington Louisiana 70433
Clinical Trials Management, LLC Metairie Louisiana 70006
Women Under Study, LLC New Orleans Louisiana 70125
Tolan Park Medical Building Detroit Michigan 48201
Consultants in Women's Healthcare, Inc. St Louis Missouri 63131
Lawrence OB/GYN Clinical Research, LLC Lawrenceville New Jersey 08648
Women's Health Research Center Plainsboro New Jersey 08536
Unified Women's Clinical Research - Central Carolina Greensboro North Carolina 27408
Wake Research Associates, LLC Raleigh North Carolina 27612
Drexel University Philadelphia Pennsylvania 19102
Medical Research South, LLC Charleston South Carolina 29407
WR-Medical Research Center of Memphis, LLC Memphis Tennessee 38120
Tmc Life Research, Inc. Houston Texas 77054
Clinical Trials of Texas, Inc. San Antonio Texas 78229
Seattle Women's Health, Research, Gynecology Seattle Washington 98105

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 NCT03253094, 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 Aug 11, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03253094 live on ClinicalTrials.gov.

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