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BESPONSA® (inotuzumab ozogamicin)

BESPONSA is indicated as monotherapy for the treatment of adults with relapsed or refractory CD22-positive B cell precursor acute lymphoblastic leukaemia (ALL). Adult patients with Philadelphia chromosome positive (Ph+) relapsed or refractory B cell precursor ALL should have failed treatment with at least 1 tyrosine kinase inhibitor (TKI).1

Clinical Study Results

The efficacy and safety of BESPONSA were evaluated in a Phase 3 clinical trial vs standard chemotherapy.1,2

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BESPONSA Safety Profile

Review the safety profile of BESPONSA.1

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Dosing & Administration

Besponsa is a 1-hour IV infusion and can conveniently be administered in the outpatient setting.1,3

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Besponsa Prescribing Information
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ALL=acute lymphoblastic leukemia; CD=cluster of differentiation; CR=complete remission; EMD=extramedullary disease; Ph+=Philadelphia chromosome-positive; R/R=relapsed/refractory; SmPC=Summary of Product Characteristics; TKI=tyrosine kinase inhibitor.
References:Besponsa Summary of Product CharacteristicsKantarjian HM, DeAngelo DJ, Stelljes M, et al.. N Engl J Med. 2016;375(8):740-753.Marks DI, et al. Cancer Med. 2019;8(13):5959-5968

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Further information is available upon request

PP-INO-IRL-0104 January 2023

Adverse events should be reported. Report an adverse event to your national reporting system (HPRA Pharmacovigilance)

Adverse events should also be reported to Pfizer Medical Information on 1800 633 363

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