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ACTIVE NOT RECRUITING
NCT07571824
PHASE1

A Study to Assess the Bioavailability and Adhesion of Selegiline TDS in Healthy Subjects

Sponsor: Corium Innovations, Inc.

View on ClinicalTrials.gov

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

Interventions

DRUG

Selegiline TDS 6 mg/24 hours

Selegiline TDS 6 mg/24 hours

DRUG

EMSAM® TDS 6 mg/24 hours

EMSAM® TDS 6 mg/24 hours

Locations (1)

Novum Pharmaceutical Research Services

Las Vegas, Nevada, United States