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Retention and Duration of Activity of SPL7013 (VivaGel®) After Vaginal Dosing.

HIV Infections Clinical Trial

Official title:
Assessment of Local Retention and Duration of Activity of SPL7013 Following Vaginal Application of 3% SPL7013 Gel (VivaGel) in Healthy Volunteers

Clinical Trial Summary

To assess the retention and anti-viral activity (human immunodeficiency virus (HIV) and herpes simplex virus 2 (genital herpes, HSV-2) of SPL7013 in cervicovaginal samples taken up to 24 hours after administration of 3% SPL7013 in the vagina. There is no hypothesis for this study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00740584
Study type Interventional
Source Starpharma Pty Ltd
Contact
Status Completed
Phase Phase 1/Phase 2
Start date August 2008
Completion date March 2009
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