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Anticholinergic
Clinical Study to Assess the Efficacy and Safety of AT-5214 in the Treatment of Subjects With Palmar Hyperhidrosis
Phase 2
Waitlist Available
Research Sponsored by Atacama Therapeutics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 6 (end of study)
Summary
This trial tests AT-5214 tablets on people with very sweaty palms to see if it can reduce their sweating. The study will compare two doses of the medication.
Eligible Conditions
- Sweaty palms
- Excessive Sweating
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ week 6 (end of study)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 6 (end of study)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
PHIS Reduction
Secondary study objectives
Absolute change in PHIS
Absolute change of Sweat Production
Change in Sweat Production
Trial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: Low Dose (2 mg)Experimental Treatment1 Intervention
Oral tablet containing 1 mg of active drug, dexmecamylamine HCl. Subjects will be instructed to take two tablets by mouth twice daily (in the morning and evening).
Group II: High Dose (4 mg)Experimental Treatment1 Intervention
Oral tablet containing 2 mg of active drug, dexmecamylamine HCl. Subjects will be instructed to take two tablets by mouth twice daily (in the morning and evening).
Group III: PlaceboPlacebo Group1 Intervention
Oral tablet containing no active drug. Subjects will be instructed to take two tablets by mouth twice daily (in the morning and evening).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Dexmecamylamine
Not yet FDA approved
Find a Location
Who is running the clinical trial?
Atacama TherapeuticsLead Sponsor
1 Previous Clinical Trials
60 Total Patients Enrolled