New data suggest that Kyowa Kirin Co., Ltd./MEI Pharma, Inc.’s PI3K inhibitor zandelisib has better-than-expected efficacy data and a favorable safety profile that could position it as a top player in a class whose members have often suffered from safety issues.
MEI and Kyowa Kirin announced 30 November interim data from their single-arm, Phase II TIDAL study testing zandelisib as a monotherapy in relapsed/refractory follicular lymphoma (FL). The two companies announced a partnership in October 2018 to develop the drug, and in April 2020 signed a $683m deal giving Kyowa Kirin rights in most global markets, along with co-development and sharing of profits and costs in the US
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