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inotuzumab

This page shows the latest inotuzumab news and features for those working in and with pharma, biotech and healthcare.

NICE to look again at Pfizer’s Besponsa after appeal

NICE to look again at Pfizer’s Besponsa after appeal

Last August, NICE turned down Besponsa (inotuzumab ozogamicin) for routine use on the National Health Service for adults with relapsed or refractory CD22-positive B-cell precursor acute lymphoblastic leukaemia (ALL) ... Pfizer is committed to ongoing

Latest news

  • NICE set to reject Pfizer's leukaemia drug Besponsa NICE set to reject Pfizer's leukaemia drug Besponsa

    The National Institute of Healthcare and Excellence (NICE) is set to reject Pfizer’s orphan drug for leukaemia Besponsa (inotuzumab ozogamicin). ... David Montogomery, oncology medical director at Pfizer UK, said: “[This] frustrating decision for

  • FDA clears Pfizer's leukaemia drug Besponsa FDA clears Pfizer's leukaemia drug Besponsa

    Europe. Besponsa (inotuzumab ozogamicin), which had breakthrough status, was approved after a priority review by the FDA as this type of leukaemia is aggressive, has a very poor prognosis in adults, ... care. The rate of complete remission was

  • NICE rejects Pfizer's antibody drug for leukaemia NICE rejects Pfizer's antibody drug for leukaemia

    Evidence from clinical trial data showed no survival benefit from Besponsa (inotuzumab ozogamicin) compared to current treatment said NICE, although it noted that more people who were treated with Pfizer's ... David Montgomery, oncology medical director

  • CHMP backs two rare disease therapies at April meeting CHMP backs two rare disease therapies at April meeting

    In other news from the CHMP meeting, Pfizer picked up a positive opinion for Besponsa (inotuzumab ozogamicin) as a single-agent treatment for adults with relapsed or refractory CD22-positive

  • FDA verdict on Pfizer's breakthrough leukaemia drug due in August FDA verdict on Pfizer's breakthrough leukaemia drug due in August

    care. The rate of complete remission was significantly higher in the inotuzumab ozogamicin group than in a group treated with standard chemotherapy - 81% versus 29%, respectively. ... The FDA is scheduled to deliver a verdict on Pfizer's application in

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