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HuMax-CD20 in Active Rheumatoid Arthritis

2014-08-27 03:46:05 | BioPortfolio

Summary

The purpose of this study is to evaluate the safety and effectiveness of HuMax-CD20 in patients with active Rheumatoid Arthritis.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Conditions

Acute Rheumatic Arthritis

Intervention

Placebo, Active comparator 300 mg, Active comparator 700 mg, Active comparator 1000 mg

Location

The University of Alabama at Birmingham
Birmingham
Alabama
United States
35294

Status

Completed

Source

Genmab

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:46:05-0400

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