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Clinical Trial Summary

This phase I/IIa study has an open-label, First-in-Human (FIH), single center design to assess the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of multiple doses of topically applied CLS003 in healthy subjects with cutaneous warts.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02106260
Study type Interventional
Source Cutanea Life Sciences, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 2014

See also
  Status Clinical Trial Phase
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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 NCT02333643 - A Phase 2 Efficacy Study of CLS003 ICVT in Subjects With Cutaneous Warts. Phase 2
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