Trial Evaluating Safety, Tolerability and Immune Response of AG-707

Summary

This is a randomized, multi-center, sequential, dose-escalating study of three dose cohorts of AG-707. Individuals who meet all of the inclusion and exclusion criteria for eligibility will be randomized to receive either AG-707 (at the 80 µg dose), AG-707 with QS-21 (at the 80 µg dose), placebo, or QS-21. Each patient will be monitored for safety as specified in the protocol.

Timeline

Start

2006-03

Primary completion

—

Completion

—

Drugs

Indications