A double blind, phase I/II, randomized, single and repeat dose, dose escalation study of the antibody BI-201 directed against Tat, given IV, versus Placebo in asymptomatic HIV-1 patients.

Registry ID
EUCTR2005-001019-23
Source registry
EUCTR
Status
Completed
Phase
PHASE2
Sponsor
BioInvent International AB
Start date
2005-05-11
Completion date
2006-02-07
Last update
2026-08-16

Conditions

Summary

To monitor tolerability after single IV doses and after a short repeat dose regimen with initial loading doses (to achieve a rapid steady state serum level).

Locations

View on source registry