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Leveraging innate cell engagers for lymphoma treatment

European Pharmaceutical Review

We received encouraging feedback from the US Food and Drug Administration (FDA) on the trial design and potential for accelerated approval. We also believe that bispecifics will further establish themselves as an important drug class in the treatment regimens for both haematological malignancies and solid tumours.

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Moving towards oral delivery of biologics

European Pharmaceutical Review

Of the 175 new drugs approved by the US Food and Drug Administration (FDA) between 2016 and 2019, most were biologics. Of the 175 new drugs approved by the US Food and Drug Administration (FDA) between 2016 and 2019, most were biologics.