drugset / Trial / NCT02759042

An Expanded Access Protocol for a Single Subject Who Has Completed 24-Weeks of Treatment in PR0140_CD02 Study

NCT02759042 ↗

Expanded access No longer available CytoDyn, Inc. Amarex Clinical Research · collab

Summary

The primary objective is to provide continued access to PRO 140 to a subject who has completed participation in PRO140\_CD02.

Timeline

Start
—
Primary completion
—
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Background Leronlimab Monoclonal antibody — Subcutaneous