Study With a Topical Gel to Treat Common Warts in Adults

NCT ID: NCT00117871

Last Updated: 2007-02-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-10-31

Brief Summary

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The primary purpose of this study is to evaluate the effectiveness in adults of 2 different strengths of resiquimod gel applied to common wart(s) five times a week for up to 12 weeks.

A second purpose is to evaluate the safety of the drug.

Detailed Description

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Conditions

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Warts

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Interventions

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Resiquimod

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of common warts
* Two forms of birth control

Exclusion Criteria

* Pregnant or breast feeding
* Other types of warts, ie. plantar
* Currently participating in another clinical study
* Chronic viral hepatitis B or C
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Graceway Pharmaceuticals, LLC

INDUSTRY

Sponsor Role lead

Locations

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Minnesota Clinical Study Center

Fridley, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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1515-RESI

Identifier Type: -

Identifier Source: org_study_id

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