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Nurix has enrolled the first patient in the global P-III (DAYBreak CLL-306) study assessing bexobrutideg in pts with r/r chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) who have previously received a covalent BTK inhibitor
The trial, conducted under the collaboration between Nurix and Roche, is expected to enroll ~620 pts, where they will be randomized to receive either bexobrutideg (600mg, PO, QD) or pirtobrutinib
Bexobrutideg is also being evaluated as monotx. in the P-II (DAYBreak CLL-201) trial in r/r CLL and P-Ia/Ib (NX-5948-301) trial in r/r B-cell malignancies, plus in combination in P-I/II (NX-5948-203) trial for r/r and treatment naΓ―ve CLL
Ref: Globenewswire | Image: Nurix Therapeutics | Press Release
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The post Nurix Therapeutics Enrolled First Patient in P-III (DAYBreak CLL-306) Trial of Bexobrutideg in R/R CLL/SLL appeared first on PharmaShots.
