drugset / Trial / NCT00740584
Retention and Duration of Activity of SPL7013 (VivaGel®) After Vaginal Dosing.
Phase 1/2
Completed
12 enrolled
Starpharma Pty Ltd
National Institute of Allergy and Infectious Diseases (NIAID) · collab
NaSingle-groupOpen-labelTreatment
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.
Timeline
- Start
- 2008-08
- Primary completion
- 2009-03
- Completion
- 2009-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SPL7013 | Other / unclassified | 3 % | Other |