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Topical Gel
Efficacy and Safety Study of VB-1953 Topical Gel for Inflammatory Facial Acne Vulgaris
Phase 2
Waitlist Available
Research Sponsored by Vyome Therapeutics Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Summary
This trial aims to find the best way to reduce acne symptoms in males and non-pregnant females.
Eligible Conditions
- Acne Vulgaris
- Acne
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Inflammatory lesion counts
Secondary study objectives
Investigator's Global Assessment of Inflammatory Acne (IGA) score
Percent change in inflammatory lesion counts
Trial Design
4Treatment groups
Experimental Treatment
Placebo Group
Group I: VB-1953 topical gel - 2% QDExperimental Treatment1 Intervention
VB-1953 topical gel - 2% QD
Group II: VB-1953 topical gel - 2% BIDExperimental Treatment1 Intervention
VB-1953 topical gel - 2% BID
Group III: VB-1953 VehiclePlacebo Group1 Intervention
VB-1953 topical gel- 0% (Vehicle) BID
Group IV: VB-1953 topical gel- 0% (Vehicle) QDPlacebo Group1 Intervention
VB-1953 topical gel- 0% (Vehicle) QD
Find a Location
Who is running the clinical trial?
Vyome Therapeutics Inc.Lead Sponsor
Dr. Shilpi JainStudy DirectorVyome Therapeutics Inc.