Hyperhidrosis
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Showing 15 of 20 trials with date data
Clinical Trials (20)
Total enrollment: 3,920 patients across 20 trials
Excessive Sweating Caused by Antidepressants: Measurement and Treatment With Terazosin
A Study Using Botulinum Toxin Type A in Adolescents With Axillary Hyperhidrosis
A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis
Study of Glycopyrronium in Subjects With Axillary Hyperhidrosis
Long-term Safety Study of Glycopyrronium in Subjects With Primary Axillary Hyperhidrosis
Study of Glycopyrronium in Axillary Hyperhydrosis
A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis
A Confirmatory Safety and Efficacy Study of BBI-4000 in Subjects With Axillary Hyperhidrosis
A Safety, Tolerability and Preliminary Efficacy Study of BBI-4000 Gel in Subjects With Palmar Hyperhidrosis
A Study to Evaluate Clinical Effect, Pharmacokinetics , Safety, and Tolerability of Umeclidinium in Palmar Hyperhidrosis Subjects
Clinical Trial To Evaluate ANT-1207 In Participants With Primary Axillary Hyperhidrosis
A Safety and Efficacy Study of BBI-4000 in Subjects With Axillary Hyperhidrosis
Comparator Study of the Effect of Glycopyrrolate and Glycopyrronium in Subjects With Axillary Hyperhidrosis
A Dose-Ranging Study of the Effect of Glycopyrrolate in Subjects With Axillary Hyperhidrosis
Hyperhidrosis in Patients With Amputations-Botox
Hyperhidrosis, Developing a Treatment Approach Aims 1 & 2
A Safety, Tolerability and Preliminary Efficacy Study of BBI-4000 in Subjects With Axillary Hyperhidrosis
A Pilot Study Exploring the Efficacy and Safety of Topical Oxybutynin 3% Gel for Primary Focal Hyperhidrosis in Adolescents and Young Adults
A Non-Interventional Study To Assess Sweating
Safety and Efficacy of BOTOX® (Botulinum Toxin Type A) in Korea
Phase Legend
Key Insights
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.