A Study of Glycopyrronium Cloth, 2.4% in Patients With Palmar Hyperhidrosis
NCT03880266 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 72
Last updated 2021-08-25
Summary
The objective of this study is to assess the efficacy and safety of glycopyrronium cloth, 2.4% when used to treat palmar hyperhidrosis.
Conditions
- Palmar Hyperhidrosis
Interventions
- DRUG
-
Glycopyrronium cloth, 2.4%
Pre-saturated 100% polypropylene, nonwoven, fabric cloth with glycopyrronium
- DRUG
-
Vehicle
Pre-saturated 100% polypropylene, nonwoven, fabric cloth
Sponsors & Collaborators
-
Journey Medical Corporation
lead INDUSTRY
Principal Investigators
-
Kate Doherty · Dermira, Inc.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 9 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-02-22
- Primary Completion
- 2019-05-24
- Completion
- 2019-05-24
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
A Study of Norepinephrine in Patients With Congenital Insensitivity to Pain and Anhidrosis
NCT02624310 ·Status: WITHDRAWN ·Phase: PHASE2
-
Intra-Erythrocyte Dexamethasone Sodium Phosphate in Ataxia Telangiectasia Patients
NCT02770807 ·Status: COMPLETED ·Phase: PHASE3
-
NORTHERA (DROXIDOPA) for Dysautonomia in Adult Survivors of Menkes Disease and Occipital Horn Syndrome
NCT04977388 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Evaluate the Neurological Effects of EryDex on Subjects With A-T
NCT06193200 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate Multiple Ascending Dose and Multi-Dose of DT-216 in Adult Patients With Friedreich Ataxia
NCT05573698 ·Status: COMPLETED ·Phase: PHASE1
-
Phase 2a Study Examining the Safety and Efficacy of BOL-DP-o-04 for Treating Diabetic Neuropathy
NCT04082000 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
NCT00557973 ·Status: COMPLETED ·Phase: PHASE2
-
NAD+ Precursor Supplementation in Friedreich's Ataxia
NCT04817111 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patients With Spinal Muscular Atrophy
NCT00374075 ·Status: COMPLETED ·Phase: PHASE1
-
A Clinical Pharmacology Study to Evaluate the Effect of GYM329 on Disuse Muscle Atrophy in Healthy Volunteer
NCT04708847 ·Status: COMPLETED ·Phase: PHASE1
-
Crossover Study to Assess the Efficacy and Safety of UX007 in the Treatment of Movement Disorders Associated With Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS)
NCT02960217 ·Status: TERMINATED ·Phase: PHASE3
-
Study to Evaluate Sodium Phenylbutyrate in Pre-symptomatic Infants With Spinal Muscular Atrophy
NCT00528268 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Study to Evaluate DT-216 in Adult Patients With Friedreich Ataxia
NCT05285540 ·Status: COMPLETED ·Phase: PHASE1
-
A Pilot Efficacy and Safety Study of ST101 in Essential Tremor
NCT01332695 ·Status: COMPLETED ·Phase: PHASE2
-
Clinical Trial for GNX80 in Intermittent Claudication
NCT05400395 ·Status: UNKNOWN ·Phase: PHASE4
-
Pharmacological Intervention in Insulin Resistance Targeting Autonomic Nerve Activity
NCT00689208 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
A Proof of Concept Study of the Effectiveness of Carisbamate in the Treatment of Essential Tremor
NCT00524056 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Efficacy, and Tolerability of NBI-827104 for the Treatment of Essential Tremor
NCT04880616 ·Status: COMPLETED ·Phase: PHASE2
-
Upper Limb Tremor Reduction in Essential Tremor Patients
NCT06343285 ·Status: COMPLETED ·Phase: NA
-
Therapeutic Efficacy of Tiludronic Acid on Inner Ear Involvement in Advanced Otosclerosis
NCT01617057 ·Status: TERMINATED ·Phase: PHASE3
-
Sinusoidal Galvanic Vestibular Stimulation for Neurogenic Orthostatic Hypotension / Syncope
NCT04976101 ·Status: WITHDRAWN ·Phase: NA
-
A Phase 2 RCT Study of CX-8998 for Essential Tremor
NCT03101241 ·Status: COMPLETED ·Phase: PHASE2
-
4-Aminopyridine in Episodic Ataxia Type 2
NCT01543750 ·Status: WITHDRAWN ·Phase: PHASE2
-
Clinical Study of Diazoxide Choline Controlled-Release Tablet (DCCR) in Patients With Prader-Willi Syndrome
NCT02034071 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Carbidopa for the Treatment of Excessive Blood Pressure Variability
NCT02553265 ·Status: COMPLETED ·Phase: PHASE2