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FDA Approves Genentech's Columvi, the First and Only Bispecific Antibody With a Fixed-Duration Treatment for People With Relapsed or Refractory Diffuse Large B-cell Lymphoma | Business

SOUTH SAN FRANCISCO, Calif. (BUSINESS WIRE) Jun 15, 2023 ....

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FDA Approves Genentech's Columvi, the First and Only Bispecific Antibody With a Fixed-Duration Treatment for People With Relapsed or Refractory Diffuse Large B-cell Lymphoma | Region

SOUTH SAN FRANCISCO, Calif. (BUSINESS WIRE) Jun 15, 2023 ....

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FDA Approves Genentech's Polivy in Combination With R-CHP for People With Certain Types of Previously Untreated Diffuse Large B-cell Lymphoma

19.04.2023 - Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), announced today that the U.S. Food and Drug Administration (FDA) has approved Polivy (polatuzumab vedotin-piiq) in combination with Rituxan (rituximab), cyclophosphamide, . ....

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Speaking the latest language of healthcare: Digital health tech

How Embark® App combines a medical and digital approach to support patients in managing their Enbrel® (etanercept) treatment. ....

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Preparing the Classroom for Food Allergies

Preparing the Classroom for Food Allergies
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