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NCT02129660 · ClinicalTrials.gov registry record · Phase 2
Comparator Study of the Effect of Glycopyrrolate and Glycopyrronium in Subjects With Axillary Hyperhidrosis
A Phase 2 study of Hyperhidrosis, sponsored by Journey Medical Corporation.
- Completed
- Registry status
- Phase 2
- Development phase
- 105
- Enrollment target
- 15
- Study locations
NCT02129660 is a Phase 2 study of Hyperhidrosis that has completed, run by Journey Medical Corporation. The registered enrollment target is 105 participants, above the 86-participant average among 8 other Hyperhidrosis trials with a reported enrollment target (22% higher). The trial reports 15 study locations across 11 states.
The verdict
NCT02129660, a Phase 2 study of Hyperhidrosis, has completed, sponsored by Journey Medical Corporation.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 105 participants
- Enrollment target
- 15
- Study locations
Study Summary
The purpose of the study is to assess the safety of 2 doses of glycopyrrolate compared to 2 doses of glycopyrronium and vehicle (5 treatment arms) for the treatment of axillary hyperhidrosis when applied once daily for 4 weeks followed by a 2-week post-dose period.
Conditions Studied
Interventions
- OTHER Vehicle
- DRUG Dose 1 of glycopyrrolate, 2.0% QD
- DRUG Dose 2 of glycopyrrolate, 3.0% QD
- DRUG Dose 1 of glycopyrronium, 2.5% QD
- DRUG Dose 2 of glycopyrronium, 3.75% QD
Study Locations (15)
Washington
- Dermatology Associates - Seattle
- Women's Clinical Research Center - Seattle
- Premier Clinical Research - Spokane
California
- California Dermatology & Clinical Research Institute - Encinitas
- Center For Dermatology Clinical Research - Fremont
Florida
- Olympian Clinical Research - Tampa
- Kenneth R. Beer MD - West Palm Beach
Indiana
- Shideler Clinical Research Center - Carmel
Missouri
- Saint Louis University Dermatology - St Louis
Ohio
- Haber Dermatology and Cosmetic Surgery - Beachwood
Tennessee
- Rivergate Dermatology Clinical Research Center, PLLC - Goodlettsville
Texas
- DermResearch, Inc - Austin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 105 participants |
| Start Date | 2014-04 |
| Est. Completion | 2015-01 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02129660
The ClinicalTrials.gov registry entry for NCT02129660 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 105 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 86-participant average among 8 other Hyperhidrosis trials with a reported enrollment target (22% higher). The listed sponsor is Journey Medical Corporation, which has 9 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Hyperhidrosis appearing as the primary indexed condition, and to 5 interventions - of which Vehicle is the first listed.
NCT02129660 reports 15 study locations spanning 11 distinct geographic areas - top geographies include Washington, California, Florida.
Frequently Asked Questions
What is clinical trial NCT02129660 about?
NCT02129660 is a clinical study titled "Comparator Study of the Effect of Glycopyrrolate and Glycopyrronium in Subjects With Axillary Hyperhidrosis". The purpose of the study is to assess the safety of 2 doses of glycopyrrolate compared to 2 doses of glycopyrronium and vehicle (5 treatment arms) for the treatment of axillary hyperhidrosis when applied once daily for 4 weeks followed by a 2-week post-dose period.
What is the current status of trial NCT02129660?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 105 participants. The study started on 2014-04. Estimated completion is 2015-01.
What conditions does trial NCT02129660 study?
This clinical trial studies the following conditions: Hyperhidrosis.
What interventions are being tested in trial NCT02129660?
The interventions under investigation include: Vehicle (OTHER), Dose 1 of glycopyrrolate, 2.0% QD (DRUG), Dose 2 of glycopyrrolate, 3.0% QD (DRUG), Dose 1 of glycopyrronium, 2.5% QD (DRUG), Dose 2 of glycopyrronium, 3.75% QD (DRUG).
Who is sponsoring clinical trial NCT02129660?
This trial is sponsored by Journey Medical Corporation, which has 9 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02129660 being conducted?
This trial has 15 study locations across California, Florida, Indiana, Missouri, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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