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Female Sexual Dysfunction

1
Pipeline Programs
3
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
1
0
0
0
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Pfizer
PfizerNEW YORK, NY
1 program
1
PF-00446687Phase 21 trial
Active Trials
NCT00479570Completed23Est. Feb 2008
Human BioSciences
Human BioSciencesWV - Martinsburg
1 program
Sympathetic manipulation on sexual arousal in womenN/A1 trial
Active Trials
NCT00142714Unknown70Est. Jun 2005
Leadiant Biosciences
Leadiant BiosciencesMD - Rockville
1 program
Syntocinon NasalsprayPHASE_21 trial
Active Trials
NCT02229721Completed30Est. Oct 2013

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Leadiant BiosciencesSyntocinon Nasalspray
PfizerPF-00446687
Human BioSciencesSympathetic manipulation on sexual arousal in women

Clinical Trials (3)

Total enrollment: 123 patients across 3 trials

NCT02229721Leadiant BiosciencesSyntocinon Nasalspray

Effect of Chronic Intranasal Oxytocin Administration on Sexual Function in Pre- and Postmenopausal Women

Start: Jun 2012Est. completion: Oct 201330 patients
Phase 2Completed

Study To Investigate Effect Of A New Drug (PF-00446687) In Post-Menopausal Women Who Suffer From Sexual Dysfunction.

Start: Jun 2007Est. completion: Feb 200823 patients
Phase 2Completed
NCT00142714Human BioSciencesSympathetic manipulation on sexual arousal in women

Effects of Spinal Cord Injury on Female Sexual Response

Start: Aug 2003Est. completion: Jun 200570 patients
N/AUnknown

Phase Legend

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

Key Insights

3 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.