GSK’s Myeloma Drug Gets AdComm Backing, But Limitations Remain Clear

Likely To Be First BCMA Approval

The antibody-drug conjugate now looks set for US approval, but its limitations leave plenty of scope for CAR-T and bispecific rivals.

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GSK is looking to break back into the oncology market

GlaxoSmithKline plc’s BCMA-directed antibody-drug conjugate belantamab mafodotin has received a unanimous vote in favor of approval from a US Food and Drug Administration advisory committee as a treatment for relapsed or refractory multiple myeloma.

This was despite trial data showing it can cause a serious eye problem, keratopathy, in patients, with a pre-meeting review...

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