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Clinical Trial Summary

A phase 2, randomized, vehicle-controlled, double-blind study to assess the efficacy, safety and pharmacodynamics (PD) of topically applied CLS003 in otherwise healthy patients with cutaneous warts.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02333643
Study type Interventional
Source Cutanea Life Sciences, Inc.
Contact
Status Completed
Phase Phase 2
Start date January 2015
Completion date August 2015

See also
  Status Clinical Trial Phase
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Completed NCT02106260 - First-in-Human Study of CLS003 ICVT in Subjects With Cutaneous Warts Phase 1/Phase 2
Recruiting NCT00644579 - bLAC - Treatment of Cutaneous Warts in Immune Suppressed, Kidney Transplanted Patients Phase 2
Completed NCT03846648 - CyPep-1 in Cutaneous Warts Phase 1
Not yet recruiting NCT05902624 - Efficacy and Safety of Hepatitis B Virus Vaccine(HBV) in Treatment of Cutaneous Warts Early Phase 1
Completed NCT05023408 - Intralesional Bleomycin Versus Cryotherapy for Treatment of Cutaneous Warts Phase 2
Completed NCT05862441 - A Study to Assess the Efficacy of Omnivirol-Salicylic Acid Combination Therapy for Cutaneous Warts With Emphasis on Persistent Warts Phase 2/Phase 3
Completed NCT03734003 - Infrared Bioeffect System for the Treatment of Cutaneous Warts N/A