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

Exclusion Criteria

• •1. Positive test results for syphilis, hepatitis (HbsAg, anti-HCV), HIV infection, gonococcal infection, urogenital trichomoniasis, chlamydial infection, inflammatory diseases of the urogenital system caused by genital mycoplasmas.
• •2. Unsystematic use of barrier methods of contraception.
• •3. Pregnancy and lactation.
• •4. Known allergic reactions to interferons and / or other significant allergic diseases.
• •5. Any immunotropic therapy within the last 6 weeks prior to enrollment in the study.
• •6. The need to take drugs prohibited during the study.
• •7. Condition after organ transplantation, constant intake of immunosuppressive drugs.
• •8. Severe pathology from the cardiovascular system (uncontrolled arterial hypertension, unstable angina pectoris, congestive heart failure, cardiac arrhythmias), a history of myocardial infarction or cerebrovascular accident within the last 6 months.
• •9. Severe pathology on the part of the liver (increased content of AST, ALT 2 times higher than the upper limit of the norm, the content of total bilirubin\> 2 mg / dL), kidney (content of creatinine\> 1.5 mg / dL); signs of hepatic and / or renal failure.
• •10. The presence of severe pathology on the part of the respiratory system, gastrointestinal tract, hematopoietic system.
• •11. Other serious (acute or chronic) pathological conditions, including mental illness, as well as abnormalities in laboratory parameters, which, in the opinion of the investigator, may increase the risk associated with participation in the study or affect the interpretation of efficacy and safety data obtained in this research.
• •12. Alcohol and / or drug dependence.
• •13. Participation in other clinical trials in the last three months prior to inclusion.