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FDA approves Roche's Alecensa as the first adjuvant treatment for people with ALK-positive early-stage lung cancer - Vimarsana News

FDA approves Roche's Alecensa as the first adjuvant treatment for people with ALK-positive early-stage lung cancer

Approval based on Phase III ALINA study showing Alecensa reduced the risk of disease recurrence or death by an unprecedented 76% in people with ALK-positive early-stage resected non-small cell lung...

Study Examining Glofitamab With GemOX in Patients With R/R DLBCL Meets Primary Endpoint - Vimarsana News

Study Examining Glofitamab With GemOX in Patients With R/R DLBCL Meets Primary Endpoint

Previously, glofitamab had received an accelerated approval for patients with relapsed or refractory diffuse large B-cell lymphoma who received 2 or more prior lines of systemic therapy.

South San Francisco seeks experience, discussions from the STEM industry - Vimarsana News

South San Francisco seeks experience, discussions from the STEM industry

South City is a biotech hotbed, home to multinational firms like Genentech and Amgen, but there still remain large segments of the area’s population that are less inclined to enter

FDA Approves Alectinib to Treat Patients With ALK-Positive NSCLC - Vimarsana News

FDA Approves Alectinib to Treat Patients With ALK-Positive NSCLC

With this approval, alectinib is the first anaplastic lymphoma kinase inhibitor to be approved for patients with ALK-positive, early-stage non-small cell lung cancer.

Columvi Plus GemOx May Improve Survival in R/R DLBCL - Vimarsana News

Columvi Plus GemOx May Improve Survival in R/R DLBCL

The phase 3 STARGLO study met its primary endpoint of improved overall survival, according to Columvi’s manufacturer, Genetech.