drugset / Trial / NCT01610050

A Phase I Study of LFA102 in Japanese Patients

NCT01610050 ↗

Phase 1 Completed 14 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate safety and tolerability to determine the MTD/RD.

Timeline

Start
2012-06
Primary completion
2014-02
Completion
2014-02

Drugs

EvaluationDrugModalityDoseRoute
Subject LFA102 Monoclonal antibody — Intravenous