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A Study to Assess the Bioavailability and Adhesion of Selegiline TDS in Healthy Subjects
Sponsor: Corium Innovations, Inc.
Summary
The purpose of this research study is to compare the bioavailability and adhesion of a generic Selegiline transdermal system (TDS) against the marketed comparator (EMSAM®) in healthy volunteers. Systemic and local safety and tolerability will be also observed and evaluated.
Official title: A Study to Compare the Bioequivalence and Adhesion Between a Test Selegiline Transdermal Delivery System (TDS) and Reference EMSAM® (Selegiline TDS) at the Same Strength (6 mg/24 Hours) for 24 Hours in Healthy Adult Subjects
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
92
Start Date
2026-03-23
Completion Date
2026-07-29
Last Updated
2026-05-28
Healthy Volunteers
Yes
Conditions
Interventions
Selegiline TDS 6 mg/24 hours
Selegiline TDS 6 mg/24 hours
EMSAM® TDS 6 mg/24 hours
EMSAM® TDS 6 mg/24 hours
Locations (1)
Novum Pharmaceutical Research Services
Las Vegas, Nevada, United States