drugset / Trial / NCT00838565

Phase I Study Of The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of Multiple Intravenously Administered Doses Of PF-04236921 In Patients With Rheumatoid Arthritis

NCT00838565 ↗

Phase 1 Completed 41 enrolled Pfizer
RandomizedParallel-groupDouble-blindOther

Summary

This study will evaluate the safety and tolerability of PF-04236921 administered monthly as three intravenous infusions. Each group of patients will be assigned to a dose level; Safety and tolerability of a low dose level will be required before proceeding to successively higher dose levels. Blood tests will be performed to measure the amount of drug and changes in measures of inflammation.

Timeline

Start
2009-05-20
Primary completion
2012-02-02
Completion
2012-02-02

Drugs

EvaluationDrugModalityDoseRoute
Subject PACIBEKITUG Monoclonal antibody — Intravenous

Indications