Glizigen-Viudid-External Anogenital Warts in Children and Adolescents

2014-08-27 03:14:11 | BioPortfolio


The purpose of the study is to assess the efficacy of Glizigen and Viusid administration in the treatment of external anogenital warts in children and adolescents. The duration of this double-blind placebo controlled phase 3 clinical trial will be 12 weeks. The estimated number of persons to be recruited and randomized for the study is 76. Variables to be assessed will be: time to disappearance of lesions, reduction of the number of lesions and change in the aspect of lesions.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


External Anogenital Warts


Glizigen + Viusid, Placebo


Pediatric Hospital "Dr. Juan Manuel Márquez".


Not yet recruiting


Catalysis SL

Results (where available)

View Results


Published on BioPortfolio: 2014-08-27T03:14:11-0400

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Medical and Biotech [MESH] Definitions

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