Overview

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Dose CFZ533 in Rheumatoid Arthritis Patients

Status:
Completed
Trial end date:
2017-02-03
Target enrollment:
Participant gender:
Summary
This is a first-in-human study to investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single intravenous and subcutaneous doses of CFZ533 in healthy subjects and intravenous doses in rheumatoid arthritis patients.
Phase:
Phase 1
Details
Lead Sponsor:
Novartis Pharmaceuticals