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F Hoffmann-La Roche Ltd: FDA accepts application for Roche s Port Delivery System with ranibizumab (PDS) for treatment of neovascular or wet age-related macular degeneration (nAMD)

F Hoffmann-La Roche Ltd: FDA accepts application for Roche s Port Delivery System with ranibizumab (PDS) for treatment of neovascular or wet age-related macular degeneration (nAMD)
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F Hoffmann-La Roche Ltd: Roche data at EAN 2021 showcase significant impact of therapies across diverse neuroscience portfolio

F Hoffmann-La Roche Ltd: Roche data at EAN 2021 showcase significant impact of therapies across diverse neuroscience portfolio
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Investegate |F Hoffmann-La Roche Ltd Announcements | F Hoffmann-La Roche Ltd: Roche presents latest advances with immunotherapies in non-Hodgkin lymphoma

Roche presents latest advances with immunotherapies in non-Hodgkin lymphoma Data for investigational CD20xCD3 bispecific antibodies and new combination regimens with Polivy showed enhanced clinical benefits for people with non-Hodgkin lymphoma in early studies Basel, 4 June 2021 ‒ Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that new data on its investigational CD20xCD3 T-cell engaging bispecific antibodies, mosunetuzumab and glofitamab, and its first-in-class anti-CD79b antibody-drug conjugate, Polivy® (polatuzumab vedotin), in non-Hodgkin lymphoma (NHL) will be presented at the 2021 ASCO Annual Meeting from 4-8 June 2021. “People with difficult-to-treat blood cancers such as non-Hodgkin lymphoma still need more options to help improve outcomes,” said Levi Garraway, M.D., Ph.D., Roche’s Chief Medical Officer and Head of Global Product Development. “We are encouraged by promising data from our emerging T-cell engaging bispecific antibodies, mosunetuzumab and g

F Hoffmann-La Roche Ltd: Roche presents latest advances with immunotherapies in non-Hodgkin lymphoma

Data for investigational CD20xCD3 bispecific antibodies and new combination regimens with Polivy showed enhanced clinical benefits for people with non-Hodgkin lymphoma in early studies Basel, 4 June

F Hoffmann-La Roche Ltd: European Commission approves Venclyxto-based combinations for adults with newly diagnosed acute myeloid leukaemia who are ineligible for intensive chemotherapy

F. Hoffmann-La Roche Ltd: European Commission approves Venclyxto-based combinations for adults with newly diagnosed acute myeloid leukaemia who are ineligible for intensive chemotherapy leukaemia azacitidine significantly improved overall survival in patients ineligible for intensive chemotherapy, a patient population who typically have a five-year overall survival rate of less than 10% 1 Venclyxto -based combinations to provide clinically meaningful benefits in difficult to treat blood cancers Basel, 25 May 2021 - Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the European Commission has approved Venclyxto (venetoclax) in combination with hypomethylating agents, azacitidine and decitabine, for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (AML) who are ineligible for intensive chemotherapy.

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