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Trials / Completed

CompletedNCT02106260

First-in-Human Study of CLS003 ICVT in Subjects With Cutaneous Warts

A Phase I/IIa Open-label First-in-Human Study to Assess Safety and Pharmacokinetics and Explore Biomarker Effects of Topical Ionic Contra-viral Therapy (ICVT) Comprised of CLS003 in Subjects With Cutaneous Warts

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Maruho Co., Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGCLS003

Timeline

Start date
2014-03-01
Primary completion
2014-04-01
First posted
2014-04-08
Last updated
2014-05-23

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT02106260. Inclusion in this directory is not an endorsement.

First-in-Human Study of CLS003 ICVT in Subjects With Cutaneous Warts (NCT02106260) · Clinical Trials Directory