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Completed Phase 2 Interventional Results available

A Dose-Ranging Study of the Effect of Glycopyrrolate in Subjects With Axillary Hyperhidrosis

ClinicalTrials.gov ID: NCT02016885

Public ClinicalTrials.gov record NCT02016885. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 3:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-Blind, Vehicle Controlled, Dose-Ranging Study of the Effect of Glycopyrrolate in Subjects With Axillary Hyperhidrosis

Study identification

NCT ID
NCT02016885
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Journey Medical Corporation
Industry
Enrollment
198 participants

Conditions and interventions

Conditions

Interventions

  • glycopyrrolate, 1.0% Drug
  • glycopyrrolate, 2.0% Drug
  • glycopyrrolate, 3.0% Drug
  • glycopyrrolate, 4.0% Drug
  • Vehicle Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2013
Primary completion
Aug 31, 2014
Completion
Aug 31, 2014
Last update posted
Aug 24, 2021

2013 – 2014

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Burke Pharmaceutical Research Hot Springs Arkansas 71913
Gary M. Petrus, MD, PA Little Rock Arkansas 72202
California Dermatology & Clinical Research Institute Encinitas California 92024
Center For Dermatology Clinical Research Fremont California 94538
Florida Academic Dermatology Center Miami Florida 33136
Kenneth R. Beer, MD, PA West Palm Beach Florida 33401
Shideler Clinical Research Center Carmel Indiana 46032
Cypress Medical Research Center, LLC Wichita Kansas 67226
Minnesota Clinical Study Center Fridley Minnesota 55432
Saint Louis University Dermatology St Louis Missouri 63122
Skin Specialists, PC Omaha Nebraska 68144
The Dermatology Group, PC Verona New Jersey 07044
Oregon Medical Research Center Portland Oregon 97223
J&S Studies, Inc. College Station Texas 77845
Clinical Trials of Texas, Inc. San Antonio Texas 78229
Dermatology Research Center, Inc. Salt Lake City Utah 84117
Virginia Clinical Research, Inc. Norfolk Virginia 23507
Westend Dermatology Associates Richmond Virginia 23233
Dermatology Associates Seattle Washington 98101
Women's Clinical Research Center Seattle Washington 98105
Premier Clinical Research Spokane Washington 99204

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02016885, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 24, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02016885 live on ClinicalTrials.gov.

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