Clinical trial

HuMax-CD20 in Active Rheumatoid Arthritis, Phase I/II

NCT00291928 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00291928
Title HuMax-CD20 in Active Rheumatoid Arthritis, Phase I/II
Official title A Double-blind, Randomized, Placebo Controlled, Dose Escalation, Multi-centerphase I/II Trial of HuMax-CD20, a Fully Human Monoclonal Anti-CD20antibody, in Patients With Active Rheumatoid Arthritis Who Have Previously Failedone or More Disease Modifying Anti-rheumatic Drugs
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Arthritis, Rheumatoid
Intervention type Drug
Interventions Part A, Part B
Enrollment 201
Start date Feb 1, 2005
Primary completion Sep 1, 2007
Completion Sep 1, 2007
First posted Feb 15, 2006
Last update posted Nov 12, 2012

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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