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Study of the Efficacy and Safety of the Drug Ingaron (Interferon-gamma) in the Treatment of Anogenital Warts — ING-HPV-1  

Human Papillomavirus Infection Clinical Trial

Official title:
Open Controlled Randomized Study of the Efficacy and Safety of Ingaron (Interferon-gamma) in the Treatment of Anogenital Warts (Phase III)

Clinical Trial Summary

The primary purpose of this study is to evaluate the effectiveness of destructive therapy for anogenital warts in combination with the use of Ingaron in comparison with destructive therapy.

Clinical Trial Description

Literature data and the results of preclinical studies of interferon-gamma, as well as the features of HPV immunopathogenesis, show the expediency of studying the use of Ingaron in this pathology. The study was planned to include 50 outpatients of both sexes aged 18 to 50 years with a confirmed diagnosis of anogenital warts. In the course of the study, Ingaron was administered at a dose of 100,000 IU once a day every other day in the period of 10 days. Patients were divided into 2 groups: study and control. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05156541
Study type Interventional
Source SPP Pharmaclon Ltd.
Contact
Status Completed
Phase Phase 3
Start date May 18, 2009
Completion date July 15, 2010
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