drugset / Trial / NCT01480310

Study to Investigate the Safety, Pharmacokinetics, and Immunogenicity of Subcutaneous MCAF5352A in Healthy Volunteers

NCT01480310 ↗

Phase 1 Completed 23 enrolled Genentech, Inc.
RandomizedSingle-groupDouble-blindTreatment

Summary

This is a Phase Ia, randomized, double-blind, placebo-controlled, single ascending dose (SAD) study in male and female healthy volunteers, aged 18-55 years, enrolled at a single study site in Canada.

Timeline

Start
2011-12
Primary completion
2012-06
Completion
2012-06

Drugs

EvaluationDrugModalityDoseRoute
Subject AFASEVIKUMAB Monoclonal antibody — Subcutaneous

Indications

No indication recorded.