drugset / Trial / NCT04704492

A Study of the Pharmacokinetics and Safety of SM03 in Patients With Rheumatoid Arthritis

NCT04704492 ↗

Phase 1 Completed 8 enrolled SinoMab BioScience Ltd
NaSingle-groupOpen-labelTreatment

Summary

This was an open phase I trial to evaluate the pharmacokinetic, pharmacodynamic, safety and clinical activity profiles of anti-CD22 monoclonal antibody SM03 in patients with active RA.

Timeline

Start
2012-08-14
Primary completion
2013-12-16
Completion
2013-12-16

Drugs

EvaluationDrugModalityDoseRoute
Subject SM03 Monoclonal antibody 600 mg Intravenous
Subject SM03 Monoclonal antibody 900 mg Intravenous

Indications