Viewing Study NCT00115141



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Last Modification Date: 2024-10-26 @ 9:12 AM
Study NCT ID: NCT00115141
Status: COMPLETED
Last Update Posted: 2007-02-19
First Post: 2005-06-21

Brief Title: Four Week Safety and Efficacy Study With a Topical Gel to Treat Common Warts in Adults
Sponsor: Graceway Pharmaceuticals LLC
Organization: Graceway Pharmaceuticals LLC

Study Overview

Official Title: A Three-Stage Modified-Blind Dose-Escalating Study to Assess Efficacy and Safety of Resiquimod Gel Applied 3 Times Per Week for 4 Weeks for the Treatment of Common Warts in Adults
Status: COMPLETED
Status Verified Date: 2006-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The primary purpose of this study is to evaluate the effectiveness in adults of four different strengths of resiquimod gel applied to common warts three times a week for four weeks

A second purpose is to evaluate the safety of the drug
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None