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Candidiasis, Vulvovaginal

4
Pipeline Programs
4
Companies
3
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
3
0
0
1
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Bayer
BayerLEVERKUSEN, Germany
1 program
1
Clotrimazole vaginal tabletPhase 41 trial
Active Trials
NCT02180828Completed240Est. Sep 2015
Cidara Therapeutics
Cidara TherapeuticsCA - San Diego
1 program
1
CD101 Vaginal GelPhase 2
Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
1
CD101 Vaginal GelPhase 21 trial
Active Trials
NCT02733432Completed126Est. Dec 2016
Sano Chemicals
Sano ChemicalsTX - Bryan
1 program
1
OCF001 Intravaginal GelPhase 21 trial
Active Trials
NCT07521137Not Yet Recruiting36Est. Dec 2026

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
BayerClotrimazole vaginal tablet
Sano ChemicalsOCF001 Intravaginal Gel
Merck & Co.CD101 Vaginal Gel

Clinical Trials (3)

Total enrollment: 402 patients across 3 trials

NCT02180828BayerClotrimazole vaginal tablet

Clotrimazole Vaginal Tablet vs Fluconazole for Severe Vulvovaginal Candidiasis

Start: Jul 2014Est. completion: Sep 2015240 patients
Phase 4Completed
NCT07521137Sano ChemicalsOCF001 Intravaginal Gel

Biweekly Long-term Occidiofungin Study for Suppression of Mycotic Recurrence

Start: Apr 2026Est. completion: Dec 202636 patients
Phase 2Not Yet Recruiting
NCT02733432Merck & Co.CD101 Vaginal Gel

RADIANT: CD101 vs Standard of Care in Subjects With Acute Vaginal Yeast Infections

Start: Jun 2016Est. completion: Dec 2016126 patients
Phase 2Completed

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

4 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.