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🏅 FDA Orphan Designation

ARZERRA

ofatumumab

Manufacturer: Novartis Pharmaceuticals Corporation

Indicated for:
T-cell prolymphocytic leukemiaOrphanB-cell chronic lymphocytic leukemia
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Black Box Warning (Boxed Warning)

A Boxed Warning is the FDA's strongest safety warning — it indicates serious or life-threatening risks identified during clinical trials or post-market surveillance. It does not mean the medication is unsafe for all patients; your prescriber weighs these risks against the benefits for your specific situation. Source: FDA-approved prescribing information.

View full prescribing information on DailyMed (NLM) ↗

FDA-Approved Indications (2)

Treatment of chronic lymphocytic leukemia (CLL) refractory to alemtuzumab and fludarabine

for the treatment of patients with CLL refractory to fludarabine and alemtuzumab

Population: patients with CLL refractory to fludarabine and alemtuzumab

Indications & Usage

1 INDICATIONS AND USAGE Chronic Lymphocytic Leukemia (CLL) ARZERRA (ofatumumab) is indicated: in combination with chlorambucil, for the treatment of previously untreated patients with CLL for whom fludarabine-based therapy is considered inappropriate [see Clinical Studies (14.1)] in combination with fludarabine and cyclophosphamide for the treatment of patients with relapsed CLL [see Clinical Studies (14.2)] for extended treatment of patients who are in complete or partial response after at least two lines of therapy for recurrent or progressive CLL [see Clinical Studies (14.3)] for the treatment of patients with CLL refractory to fludarabine and alemtuzumab [see Clinical Studies (14.4)] ARZERRA (ofatumumab) is a CD20-directed cytolytic monoclonal antibody indicated for the treatment of chronic lymphocytic leukemia (CLL) ( 1 ): in combination with chlorambucil, for the treatment of previously untreated patients with CLL for whom fludarabine-based therapy is considered inappropriate. in combination with fludarabine and cyclophosphamide for the treatment of patients with relapsed CLL. for extended treatment of patients who are in complete or partial response after at least two lines of therapy for recurrent or progressive CLL. for the treatment of patients with CLL refractory to fludarabine and alemtuzumab.

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Medical disclaimer: This information is for educational purposes only. Always consult a qualified healthcare provider before making treatment decisions. Data sourced from FDA and current as of our last update.