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Pharmaceutical Executive Daily: FDA Approves Caplyta for Adults with Schizophrenia

Pharmaceutical Executive Daily: FDA Approves Caplyta for Adults with Schizophrenia

Published 3 weeks, 2 days ago
Description
In today's Pharmaceutical Executive Daily, Eli Lilly announces a definitive agreement to acquire Ajax Therapeutics for up to $2.3 billion, adding a first-in-class JAK2 inhibitor for blood cancers to its expanding oncology pipeline, the FDA approves a supplemental application for Johnson and Johnson's Caplyta backed by Phase III data showing a 63% reduction in relapse risk in adults with schizophrenia, and Pharmaceutical Executive speaks with Maher Masoud, CEO of MaxCyte, on moving cell and gene therapies toward commercial scale.
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