
Genentech
@genentech
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Official Twitter for Genentech. See our community guidelines here: https://t.co/yas51FPhKU
USA
Joined September 2008
#Breaking: At AAIC, we’re presenting new data in #Alzheimers, underscoring our commitment to advancing the science in this disease. Learn More:
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#Breaking: Today we announced we will advance our investigational medicine in early #ParkinsonsDisease into Phase III development. Learn more:
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#Breaking at #ASCO25: We will present Phase III data, also published in @TheLancet, for ES-SCLC, offering a potential option for this aggressive cancer. Learn more:
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#Breaking: We’re presenting new survival data for PIK3CA-mutated HR+, HER2- advanced #breastcancer at #ASCO25, also published in #NEJM. Read about the results here:
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#Breaking: We’re excited to share two-year data from our investigational BTK inhibitor for people with relapsing multiple sclerosis (RMS) presented at this year’s #CMSC2025 meeting. Learn more about the results here:
gene.com
Discover the latest news about our company, our products, our policies, and our people.
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#Breaking: The @US_FDA has approved our treatment in a new indication for #DiabeticRetinopathy (DR). Learn more about how this treatment offers a new alternative to the standard of care for people with DR:
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#Breaking: This #ESMOBreast25, we are excited to present ten-year follow-up data reinforcing the potential benefit of our treatment for HER2-positive early-stage breast cancer. Learn more:
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#Breaking: @NEJM published a detailed analysis of positive Phase III data for.our influenza treatment and household #influenza transmission. Learn more:#PublicHealth #Flu
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#Breaking: We’re presenting new data at #ADPD2025 showcasing advancements in our #Alzheimers research for the millions of people living with Alzheimer’s disease. Learn more:
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ICYMI: Our supplemental Biologics License Application for our anti-CD20 monoclonal antibody for lupus nephritis treatment was accepted by the @US_FDA. Learn more:
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ICYMI: The @US_FDA recently approved our clot-dissolving agent for the treatment of acute ischemic stroke (AIS) in adults. Read more:
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#Breaking: The @US_FDA accepted our supplemental Biologics License Application for our medicine to treat #LupusNephritis based on Phase III data showing superiority over the current standard of care. Read more here:
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#Breaking: This #AAAAI25, we’re proud to present two late-breaking oral presentations featuring new Phase III data on our medicine for patients with food allergies. Learn more:
gene.com
Discover the latest news about our company, our products, our policies, and our people.
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ICYMI: The first and only spinal muscular atrophy (#SMA) tablet has been granted approval by the FDA. Learn more:
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