EligibleTrials

Ocrelizumab: clinical trials recruiting now

7
Recruiting trials
4
Conditions studied
26
US states with sites
25
Countries

FDA drug label

FDA-approved
Yes. Ocrelizumab appears in the FDA drug-label database. Marketed as OCREVUS.
Drug class
CD20-directed Cytolytic Antibody (FDA established pharmacologic class)
Mechanism of action
CD20-directed Antibody Interactions (as stated on the FDA label)

FDA-approved use

OCREVUS is indicated for the treatment of: Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults Primary progressive MS, in adults Relapsing-remitting MS, in pediatric patients 10 years of age and older who weigh 25 kg or more. OCREVUS is a CD20-directed cytolytic antibody indicated for the treatment of: Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults ( 1 ) Primary progressive MS, in adults ( 1 ) Relapsing-remitting MS, in pediatric patients 10 years of age and older who weigh 25 kg or more ( 1 )

FDA label via openFDA

Phase breakdown

Phase 2 1 Phase 3 3 Phase 4 2 Not applicable 1

Conditions being studied

ConditionTrials
Multiple Sclerosis · Ocrelizumab for Multiple Sclerosis7
Progressive Multiple Sclerosis1
Relapsing Multiple Sclerosis1
Relapsing-remitting Multiple Sclerosis (RRMS)1

Recruiting trials involving Ocrelizumab

Common questions

Is Ocrelizumab FDA-approved?

Yes, marketed as OCREVUS.

How many recruiting trials involve Ocrelizumab?

7 recruiting trials across 4 conditions.

Is this list of trials complete?

No. For the full record, search ClinicalTrials.gov.

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