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U.S. FDA grants precedence evaluate to Roche’s bispecific antibody Glofitamab, Health News, ET HealthWorld

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Zurich: Roche introduced on Friday that the U.S. Meals and Drug Administration has granted precedence evaluate to the Swiss pharmaceutical firm’s bispecific antibody Glofitamab.

Glofitamab is meant for sufferers with relapsed or refractory massive b-cell lymphoma.

The FDA is predicted to decide on approval of the most cancers immunotherapy by July 1, 2023.

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