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Efficacy and Safety Study of Polyphenon E to Treat External Genital Warts

NCT00449982 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 480

Last updated 2007-03-21

No results posted yet for this study

Summary

The purpose of this study is to investigate the clinical efficacy, safety and tolerability of a Polyphenon E Ointment 10% and a Polyphenon E Ointment 15% in the treatment of external genitial warts in male and female patients.

Conditions

  • Condylomata Acuminata

Interventions

DRUG

Polyphenon E Ointment 10%, Polyphenon E Ointment 15%

Sponsors & Collaborators

  • MediGene

    lead INDUSTRY

Principal Investigators

  • Karl R. Beutner, M.D., Ph.D. · Solano Clinical Research, 635 Anderson Road #17, Davis CA 95616, USA

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-07-31
Completion
2004-08-31

Countries

  • United States
  • Argentina
  • Chile
  • Colombia
  • Mexico
  • Peru
  • Romania

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00449982 on ClinicalTrials.gov