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Adverse event reporting can be found at the bottom of the page
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The content of this website has been produced in line with the BESPONSA® (gemtuzumab ozogamicin) Summary of Product Characteristics for the United Kingdom. For BESPONSA® prescribing information Click here. Adverse event reporting information can be found at the bottom of the page
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
BESPONSA is recommended by NICE as an option for treating relapsed or refractory CD22-postive B-cell precursor ALL in adults2. People with relapsed or refractory Philadelphia chromosome positive disease should have had at least 1 tyrosine kinase inhibitor2.
Resources to support you
Download materials to support you with the use of BESPONSA and managing patients with ALL.
Watch this on-demand video from KOLs exploring the ALL landscape and patient case studies.
ALL , acute lymphoblastic leukaemia; B-cell ALL, B-cell acute lymphoblastic leukaemia; CAR, chimeric antigen receptor; KOL, key opinion leader; Ph-positive ALL, philadelphia chromosome-positive acute lymphoblastic leukaemia; R/R, relapsed/refractory.
References
Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk or search
for MHRA Yellow Card in Google Play or Apple App Store
Adverse events should also be reported to Pfizer Medical Information on 01304 616161
To access further materials, resources and receive communication about medicines and vaccines promoted by Pfizer.
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PP-UNP-GBR-7812. January 2024.