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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of amolimogene, in the treatment of patients with high-grade cervical intraepithelial lesions of the uterine cervix.


Clinical Trial Description

This is a double-blind study, so neither the patient not the doctor will know which treatment has been assigned. ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00264732
Study type Interventional
Source Eisai Inc.
Contact
Status Completed
Phase Phase 2/Phase 3
Start date July 2005
Completion date May 2009

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