genentech revenue 2021

FDA Approves Genentech's Lunsumio, a First-in-Class Bispecific Antibody, to Treat People With Relapsed or Refractory Follicular Lymphoma. Genentech revenue is $166.9M annually. Final analysis from the Phase IIIb STASEY study, including data from 193 people with hemophilia A, further support the benefit/risk profile of Hemlibra, with no new safety signals identified Merck continues to experience strong global underlying demand across its business. In 2022, Roche's seventh top revenue generating drug was Herceptin (trastuzumab). Newark, New Castle, USA, April 28, 2023 (GLOBE NEWSWIRE) In accordance with the most recent analysis by Growth Plus Reports, the global market for multifocal motor neuropathy is expected to expand at a revenue CAGR of 3.6% in between 2023 to 2031. Biotech startup Recursion Pharmaceuticals on Tuesday announced a mega deal with Swiss drug and diagnostics giant Roche AG, and its U.S. subsidiary Genentech, that could generate billions in new revenues for the Salt Lake City-based company in the coming decade. The data presented on this page does not represent the view of Genentech and its employees or that of Zippia. 21 Dec 2022. None of the information on this page has been provided or approved by Genentech. Genentech's Annual Report & Profile shows critical firmographic facts: What is the company's size? Genentech Presents Pivotal Data at ASH 2021 for Novel Cancer Immunotherapy Mosunetuzumab Results to be presented for the first time show mosunetuzumab induces high and durable complete response rates in people with follicular lymphoma who have received two or more prior therapies Genentech peak revenue was $166.9M in 2022. Genentech makes $457,260 in a day. . Back in 2008, Genentechs top drugs were Avastin, Rituxan, Herceptin, and Lucentis, which generated sales of over $7 billion. Description. A look at our approvals past and present. The news is another sign of both the [], Shuttle bus drivers for five tech companies -- eBay, Apple, Yahoo, Genentech and Zynga -- voted Friday afternoon to be represented byTeamsters Local 853, the union said, part of alarger pushtoward unionizingSilicon Valley's legions of support workers. Genentech may also be known as or be related to Genentech, Genentech Inc, Genentech Inc., Genentech USA Inc, Genentech USA, Inc. and Genetic Engineering Technology. Genentech's annual revenues are over $500 million (see exact revenue data) and has over 1,000 employees. Bristol Myers reported second quarter revenues of $11.7 billion, 16% higher than in the same period last year, driven in part by sales of Opdivo that exceeded $1.9 billion for the quarter, 16%. Gentex revenue for the twelve months ending December 31, 2022 was $1.919B, a 10.85% increase year-over-year. Genentech has 16 portfolio exits. Revenue codes: 0771 preventive care services, vaccine administration. As of Dec. 31, 2021, Roche had CHF 6.85 billion in cash and cash equivalents. ophthalmology, neuroscience 22 Dec 2022. [4] Historically, the company is regarded as the world's first biotechnology company. Roche's 2021 net income was CHF 14.94 billion, with core EPS of CHF 19.81 per share, compared to CHF 15.01 billion, with core EPS of CHF 19.16 per share, in 2020. [5] As of July 2021, Genentech employed 13,539 people. Industry: Biotechnology & Pharmaceuticals: Industry Vertical: Biotechnology: Founded: 1,976: HQ Location: South San Francisco, Calif. Sites: 9: U.S. Employees: 13,588 The drug generated about 2.1 billion. Chairman and CEO Letter and Amgen Inc. 2021 Annual Report 3.7 MB. Abbott $213.19 billion. After extensive research and analysis, Zippia's data science team found the following key financial metrics. . Compare BAYRY With Other Stocks. Roche Holding (NASDAQ:RHHBY) acquired Genentech, a pharmaceuticals company with three blockbuster oncology drugs, in 2009 for a sum of $47 billion. Please be aware that we do not take any responsibility for accessing such information which may not comply with any legal process, regulation, registration or usage in the country of your origin. The data on this page is also based on data sources collected from public and open data sources on the Internet and other locations, as well as proprietary data we licensed from other companies. Read more news. The Global Asthma Medication market is anticipated to rise at a considerable rate during the forecast period, between 2022 and 2030. Revenue is the top line item on an income statement from which all costs and expenses are subtracted to arrive at net income. Nine-month 2021 Presentation without appendix. Approximately three million people will die from cancer in China this year alone, Cancer will kill approximately three million people in China this year alone. It was a good year to be a pharmaceutical company, especially one that came up with a product to combat COVID-19. When its done right, impact-driven businesses can form the basis of a successful investment fund, the foundation of a strong company, or the impetus for a new initiative within a giant corporation. Peak Revenue $166.9M (2022) Revenue / Employee 2023 Genentech, Inc. All rights reserved. The pharma giant of the Midwest kicked off 2021 strong, announcing $10.5 billion in sales, a growth rate of 35.3 percent in Q1. Our pipeline includes new molecular entities that address serious unmet medical needs. As of 2018, the same This partnership has greatly influenced our students in taking a renewed excitement in STEM, shares Cherie Cohen, a SSFUSD biotech teacherHarnessing the passion and expertise of our employees is not only valuable to the students". Click on the image to the left and discover the Chiesi Group Annual and Sustainability Report 2021. Company Description: One of the world's leading biotechs, Genentech has a number of blockbuster cancer therapies based on its antibody (protein) technologies. Solutions. Genentech's Futurelab Is Growing The Next Generation Of Innovators, Keys To Running An Impact-Driven Business: Lessons From Instant Ramen, Chobani And Genentech, Genentech Brain Trust Leaves With $217 Million For New Startup To Fight Alzheimer's And Parkinson's, Bus Drivers for Apple, Yahoo, eBay, Zynga, Genentech Vote For Union Representation, Regeneron Beats Genentech In Rare Face Off Over Diabetes-Related Vision Loss, Surprise! Genentech. Marc Tessier-Lavigne Three former top researchers at Genentech, the legendary biotech that is now part of Roche Holding, have raised $217 million in venture capital to start a new company, Denali. Use Forbes logos and quotes in your marketing. The research st. Apr 16, 2020. www.sbwire.com . . Indication for PD-L1-Positive, Metastatic Triple-Negative Breast Cancer, Phase III Study Shows Genentech's Polivy Plus R-CHP is the First Regimen in 20 Years to Significantly Improve Outcomes in Previously Untreated Aggressive Form of Lymphoma Compared to Standard of Care, FDA Grants Priority Review to Genentechs Tecentriq as Adjuvant Treatment for Certain People With Early Non-Small Cell Lung Cancer, Data for Genentechs Evrysdi (risdiplam) Published in New England Journal of Medicine Shows Significant Improvement in Survival and Motor Milestones in Babies With Type 1 Spinal Muscular Atrophy (SMA), FDA Accepts Application for Genentechs Faricimab for the Treatment of Wet Age-Related Macular Degeneration (AMD) and Diabetic Macular Edema (DME), FDA Grants Breakthrough Therapy Designation for Venclexta in Combination With Azacitidine for the Treatment of Patients With Myelodysplastic Syndromes, New Data for Genentechs Hemlibra (emicizumab-kxwh) Reinforce Safety Profile in People With Hemophilia A, Genentechs Actemra Receives FDA Emergency Use Authorization for the Treatment of COVID-19 In Hospitalized Adults and Children, FDA Accepts Application for Genentechs Port Delivery System With Ranibizumab (PDS) for Treatment of Wet Age-Related Macular Degeneration (AMD), New Genentech Data for Evrysdi (risdiplam) Show Improved Motor Function in Pre-Symptomatic Babies After One Year and Confirm Safety Profile in Previously Treated People With Spinal Muscular Atrophy (SMA), Genentech Announces Data at EHA2021 Reinforcing Efficacy of Venclexta Combinations in Chronic Lymphocytic Leukemia and Acute Myeloid Leukemia, Genentech Presents Latest Advances With Immunotherapies in Non-Hodgkins Lymphoma, Pivotal Phase III Data at ASCO Show Genentechs Tecentriq Helps Certain People With Early Lung Cancer Live Significantly Longer Without Their Disease Returning, Genentech to Present Data From One of the Most Comprehensive Oncology Portfolios at the 2021 ASCO Annual Meeting Showcasing Advancements for People Living With Cancer, FDA Advisory Committee Votes in Favor of Maintaining Accelerated Approval of Genentechs Tecentriq for Previously Untreated Metastatic Bladder Cancer, FDA Advisory Committee Votes in Favor of Maintaining Accelerated Approval of Genentechs Tecentriq for PD-L1-Positive, Metastatic Triple-Negative Breast Cancer, New Data for Genentechs Ocrevus (ocrelizumab) Reinforce Significant Benefit on Slowing Disease Progression in Relapsing and Primary Progressive Multiple Sclerosis, Genentechs Evrysdi Continues to Improve Motor Function and Survival in Babies With Type 1 Spinal Muscular Atrophy (SMA), FDA Approves Xolair (omalizumab) Prefilled Syringe for Self-Injection Across All Indications, New Genentech Data at 2021 AAN Highlight Impact and Breadth of Expanding Neuroscience Portfolio, Genentech Provides Update on Tominersen Program in Manifest Huntingtons Disease, Pivotal Phase III Study Shows Genentechs Tecentriq Helped People With Early Lung Cancer Live Longer Without Their Disease Returning, New 2-Year Data Show Genentechs Evrysdi (risdiplam) Continues to Demonstrate Improvement or Maintenance of Motor Function in People Aged 2-25 With Type 2 or Type 3 Spinal Muscular Atrophy (SMA), Genentech Provides Update on the Phase III REMDACTA Trial of Actemra Plus Veklury in Patients With Severe COVID-19 Pneumonia, Genentech Provides Update on Tecentriq U.S. Long version ARCHIVE . Finance Report 2021. FDA Grants Priority Review to Genentech's Bispecific Antibody Glofitamab for People With Relapsed or Refractory Large B-Cell Lymphoma. - Senior Reporter, San Francisco Business Times Aug 30, 2021 Updated Aug 30, 2021, 2:50pm PDT Amid a closer look by regulators at cancer drugs given accelerated approval, Genentech Inc.. Why Roche Stock Moved: RHHBY Stock Has Lost 26% Since 2021 Primarily Due To Unfavorable Change In Revenues. 2021: Segments Covered: Drug Type, End user, and Region. The drug generated $7.12 billion in 2019, enough for the No. Excluding the unfavorable impact of foreign exchange of $11 million and the impact of divestitures and discontinuations of $2 million, the Bausch + Lomb segment increased organically 1,7 by . Founded more than 30 years ago, Genentech (gene.com) is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious or life threatening medical conditions. Of the world's top 20 pharmas ranked by 2021 revenues, 12 had at least 10% . Intravenous infusion, tocilizumab, for hospitalized adults . You can reach them at 1 (877) GENENTECH (436-3683) Monday-Friday, 6am-5pm PST or patientinfo@gene.com. Net income for the year was $20.8 million, down 53% on the 1991 levels. Genentech's net income for 2008 increased 14% over the previous year, while Roche experienced a . 8 spot, but as biosim challengers gained steam, sales fell to $5.32 billion in 2020. All Rights Reserved. immunology. Genentech has 13,638 employees, and the revenue per employee ratio is $12,237. . Herceptin is a drug used in the treatment of some types of breast cancer. Genentech has a clear-cut mission statement: "Work hard, play hard, and give back." The biotech giant has earned its place on Fortune's Best Companies list for 22 years. Genentech: Company Information Company Information Approvals Timeline Media Inquiries (650) 467-6800 Email Us Media / Company Information Company Information For more than 45 years, we've been following the science, seeking solutions to unmet medical needs. 2021 Group guidance unchanged Basel, July 21, 2021 - commenting on the quarter, Vas Narasimhan, CEO of Novartis, said: "Novartis delivered a strong second quarter, driven by the momentum of our key growth brands , including . Avanade has 56,000 employees, and the revenue per employee ratio is $35,714. With $60 Million Genentech Deal, 23andMe Has A Business Plan. Related by Industry: Drugs & Biotechnology, Located in San Francisco-Oakland-Fremont, CA Metropolitan Area. In the face of Roche's hostile bid, Genentech's executives are angling for a higher price. The global market for multifocal motor neuropathy was analyzed and is expected [] The company manufactures drugs using technology to bring treatments for rare diseases to patients. Avastin ended up at No. Outlook for 2021: Despite the continued strong impact of biosimilars, sales are expected to grow in the low- to mid-single digit range, at constant exchange rates. Assay Development Scientist jobs at Genentech, Control Systems Engineer jobs at Genentech, Manufacturing Production Technician jobs at Genentech, Project Manager Integrated jobs at Genentech, Senior Automation Engineer jobs at Genentech, Talent Acquisition Partner jobs at Genentech, Director Of Programs And Operations jobs at Genentech. infectious disease 2021 | 2020 | 2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 . 03.31.2020. Peak Revenue $2.0B (2022) Revenue / Employee $35,714 Avanade Jobs See insights on Genentech including office locations, competitors, revenue, financials, executives, subsidiaries and more at Craft. Genentech ended 2008 with a net income of more than $3.6 billion, versus $9.33 billion for Roche. A deal being announced today with Genentech points the way for 23andMe, the personal genetics company backed by Facebook billionaire Yuri Milner and Google Ventures to become a sustainable business even if the companys discussions with the U.S. Food and Drug Administration stretch on for [], When the US biotech company Regeneron Pharmaceuticals recently announced its first-quarter results, few were surprised that the company's flagship wet age-related macular degeneration (AMD) product Eylea had once again exceeded consensus expectations. 2021 Annual financial statements 2021 Summarised Provisional Financial Results 2021 Unaudited interim results for the six months ended 31 December 2020. Further, Roche noted that the installed base now exceeds 5,000 Cobas Liatanalyzers, which are used to run its SARS-CoV-2 and Influenza A/B point-of-care tests in about 20 minutes. Zippia gives an in-depth look into the details of Genentech, including salaries, political affiliations, employee data, and more, in order to inform job seekers about Genentech. The company, a member of the Roche Gro Read More Contact Who is Genentech Headquarters . Genentech Research and Early Development (gRED) SMA Europe 2nd International Scientific & Clinical Congress on Spinal Muscular Atrophy, Paris-Evry, 2020. Full year GAAP SG&A expense was $2,674 million as compared to $2,505 million for the full year 2020. Bayer revenue from 2010 to 2022. 05 Jan 2023. which continues to accelerate. Genentech is a biotechnology company that discovers, develops, manufactures, and commercializes medicines. Cosentyx, Entresto, Zolgensma, our Oncology portfolio and the launch of . 40 Results Our Medicines Chairman and CEO Letter and Amgen Inc. 2019 Annual Report 12.6 MB. In 2021, the company reported revenue of $18.5 billion, with GAAP net income of $12.2 billion. After extensive research and analysis, Zippia's data science team found the following key financial metrics. The biotechnology company reported ($3.78) earnings per share (EPS) for the quarter, missing the consensus estimate of ($2.50) by $1.28. After two decades of medical advancements, Sue has options to help save her sight. Safety for both If the patient was enrolled in a Medicare Advantage plan in 2020 and 2021, submit the COVID-19 vaccine and mAb infusion claims to original Medicare. Full-Year 2021 Presentation with appendix. Manufacturer of pharmaceutical products intended to focus on immunology and oncology medical fields. Product sales for TECFIDERA, AVONEX, TYSABRI and SPINRAZA each accounted for more than 10.0% of our total revenue for the years ended December 31, 2021, 2020 and 2019. Actemra is made at Genentech's largest manufacturing facility, a 400-employee plant in Vacaville that is central to a deal signed last year by the company and Regeneron Pharmaceuticals Inc.. Community Guidelines: 1. 2023 Forbes Media LLC. The additional challenges to launching new drugs that emerged since COVID-19 upended the biopharma industry, and life as we knew it, will continue into 2021, according to the annual list of. In a single month, Genentech normally makes close to $13.9M in revenue. Products. . New Data for Genentech's Hemlibra (emicizumab-kxwh) Reinforce Safety Profile in People With Hemophilia A. We want to foster positive conversation and diverse community around the issues we are passionate about. In December, Roche completed a CHF 19.0 billion repurchase of its shares held by Novartis. Sources of data may include, but are not limited to, the BLS, company filings, estimates based on those filings, H1B filings, and other public and private datasets. The employee data is based on information from people who have self-reported their past or current employments at Genentech. ophthalmology, oncology Its main products are an antibody for cancer and medicine for . (Annual sales and employees) What industry is the company in? Advanced. Was The $47 Billion Acquisition of Genentech In 2009 A Good Deal For Roche? It is classified as operating in the Medicinal & Botanical Manufacturing industry. For the fourth quarter of 1992, Genentech posted total revenues of $142 million, an increase of 18.8% on the like, year-earlier period. Discover the latest news about our company, our products, our policies, and our people. With no material changes to the operating or capital expenses, Adaptive also reaffirmed its 2021 revenue . Gentex revenue for the quarter ending December 31, 2022 was $0.494B, a 17.58% increase year-over-year. The vaccine is approved in more than 70 countries. Short version. Annual Report 2021. What is Genentech's Revenue? Today, two companies with billions at stakeGenentech and Regeneron Pharmaceuticalsare slugging it out over a trial [], This is more like it. Rituxan, another Roche . NORTH CHICAGO, Ill., Feb. 3, 2021 /PRNewswire/ -- AbbVie (NYSE: ABBV) announced financial results for the fourth quarter and full year ended December 31, 2020. [6] History The company was founded in 1976 by venture capitalist Robert A. Swanson and biochemist Herbert Boyer. Genentech General Information. The drivers' decision mirrors that of Facebook shuttle drivers, who voted for union representation [], Drug companies usually avoid head-to-head clinical trials against tough competitors. Genentech revenue is $166.9M annually. The study highlights detailed assessment of the Market and display market sizing trend by revenue & volume (if applicable), current growth factors, expert opinions, facts, and industry validated market development data. Chairman and CEO Letter and Amgen Inc. 2018 Annual Report 8.7 MB. Genentech reports positive phase 3 data for its Tecentriq combination in liver cancer Tecentriq in combination with Avastin significantly improved recurrence-free survival. Partners. JPMorgan Chase Agrees To Acquire First Republic Banks Deposits After FDIC Intervention, She Was Losing Her Vision Until Science Saved Her Sight, Memorial Sloan Kettering, Genentech, Jiahui Health To Join Forbes China Health Summit On Aug. 15, Memorial Sloan Kettering, Genentech, Jiahui Health To Join Forbes China Healthcare Summit On Aug. 15, How A Tool For Scientists Became A Billion-Dollar Opportunity. BIOGEN REPORTS FOURTH QUARTER AND FULL YEAR 2021 RESULTS Revenue: Fourth quarter $2,734 million; Full Year $10,982 million GAAP diluted EPS: Fourth quarter $2.50; Full Year $10.40 . Leading biotech and pharma product launches in 2023 and revenue forecasts for 2028 (in billion U.S. dollars) Sales share at risk of pharmaceuticals due to patent expiries U.S. 2022 Sales share at. Merck & Co. Based in Kenilworth, NJ, Merck reported $48.7 billion in sales in 2021, up 17% from the previous year, with GAAP net income of $12.345 billion. But head-to-head studies of powerful new drugs sometimes get done. Avanade peak revenue was $2.0B in 2022. Acquisitions Funding Investments News & Insights CEO Alexander Hardy CEO Approval Rating 76/100 Weigh In 1976 South San Francisco California San Francisco Bay Area Profile Last Updated: 04/18/2021 Grant Information Last Updated: 02/11/2022 Genentech, Inc. Corporate Giving Program South San Francisco, CA, United States This site is intended for US residents only. For additional financial information about our product and other revenue and geographic areas where we operate, please read Note 4, Revenue, and Note 24, Segment Information, to . 2020 Annual Financial Statements 2020 Reviewed Condensed Consolidated Annual Financial Statements 2020 Performance Measures Disclosure Document . Marc Tessier-Lavigne Three former top researchers at Genentech, the legendary biotech that is now part of Roche Holding, have raised $217 million in venture capital to start a new company, Denali Therapeutics, focused on treating and curing neurodegenerative diseases like Alzheimers, ALS, and Parkinsons. Genentech peak revenue was $166.9M in 2022. Oncology drugs revenues, which includes Herceptin, Perjeta, Tecentriq, and Avastin among other drugs, will add about $3.4 billion over 2017-2020 (29% of the $11.6 billion in incremental revenue).. Most prefer to spend their money showing they can beat a placebo, or old treatment. 5. JPMorgan Chase has agreed to assume all deposits of First Republic bank as part of a deal inked with the FDIC. This website contains information on products which is targeted to a wide range of audiences and could contain product details or information otherwise not accessible or valid in your country. The Logic Of Biologics - Is Regeneron The Next Genentech? Revenue is the top line item on an income statement from which all costs and expenses are subtracted to arrive at net income. 04.03.2019. Eight years later, Regeneron, Gilead, Genentech and hundreds of other companies use its collaborative R&D software. Indication in Prior-Platinum Treated Metastatic Bladder Cancer, Genentechs Actemra Becomes the First Biologic Therapy Approved by the FDA for Slowing the Rate of Decline in Pulmonary Function in Adults With Systemic Sclerosis-Associated Interstitial Lung Disease, a Rare, Debilitating Condition, Genentech Announces Results From Evrysdi (risdiplam) Study in Infants With Type 1 Spinal Muscular Atrophy (SMA) Published in New England Journal of Medicine, New Phase III Data Show Genentechs Faricimab Is the First Investigational Injectable Eye Medicine to Extend Time Between Treatments up to Four Months in Two Leading Causes of Vision Loss, Potentially Reducing Treatment Burden for Patients, Genentechs Faricimab Meets Primary Endpoint in Two Global Phase III Studies and Shows Potential to Extend Time Between Treatments up to 16 Weeks for People With Neovascular Age-Related Macular Degeneration, FDA Grants Priority Review to Genentechs Esbriet (pirfenidone) for Unclassifiable Interstitial Lung Disease, Genentechs Novel Anti-TIGIT Tiragolumab Granted FDA Breakthrough Therapy Designation in Combination With Tecentriq for PD-L1-High Non-Small Cell Lung Cancer, Genentechs Faricimab Meets Primary Endpoint and Shows Strong Durability Across Two Global Phase III Studies for Diabetic Macular Edema, a Leading Cause of Blindness, FDA Approves Genentechs Ocrevus (ocrelizumab) Shorter 2-Hour Infusion for Relapsing and Primary Progressive Multiple Sclerosis, Genentech Announces New Data Reinforcing the Long-Term Benefit of Venclexta-Based Combination for People With Relapsed or Refractory Chronic Lymphocytic Leukemia, Genentech Announces FDA Approval of Xolair (omalizumab) for Adults with Nasal Polyps, Genentech Announces FDA Approval of Gavreto (pralsetinib) for People With Advanced or Metastatic RET-Mutant and RET Fusion-Positive Thyroid Cancers, Genentech Announces FDA Approval of Xofluza for the Prevention of Influenza Following Contact With an Infected Person, Genentech to Present New Data Across 16 Blood Disorders at the American Society of Hematology 2020 Annual Meeting, Genentech Announces Full FDA Approval for Venclexta Combinations for Acute Myeloid Leukemia, Genentech Presents New 2-Year Data for Evrysdi (risdiplam) in Infants With Type 1 Spinal Muscular Atrophy (SMA), Genentech Presents New Data From Multiple Phase III Studies of Tecentriq in Triple-Negative Breast Cancer at ESMO Virtual Congress 2020, Genentechs Phase III EMPACTA Study Showed Actemra Reduced the Likelihood of Needing Mechanical Ventilation in Hospitalized Patients With COVID-19 Associated Pneumonia, New Data Further Reinforce Genentechs Ocrevus (ocrelizumab) as a Highly Effective Treatment for People With Multiple Sclerosis, New Data Show Genentechs Enspryng Significantly Reduces Severity and Risk of Relapse in Neuromyelitis Optica Spectrum DIsorder, Genentech Expands Its Multiple Sclerosis Portfolio With Investigational BTK Inhibitor Fenebrutinib and Initiates Novel Clinical Trials for Ocrevus (ocrelizumab), Genentech Announces FDA Approval of Gavreto (pralsetinib) for the Treatment of Adults With Metastatic RET Fusion-Positive Non-Small Cell Lung Cancer, Genentech to Present New Data in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorder at MSVirtual2020, Genentech and Regeneron Collaborate to Significantly Increase Global Supply of REGN-COV2 Investigational Antibody Combination for COVID-19, FDA Approves Genentechs Enspryng for Neuromyelitis Optica Spectrum Disorder, FDA Accepts Application for Xolair (omalizumab) Prefilled Syringe for Self-Administration Across all Indications, Genentech Provides Update on Phase III Studies of Etrolizumab in People With Moderately to Severely Active Ulcerative Colitis, FDA Approves Genentechs Evrysdi (risdiplam) for Treatment of Spinal Muscular Atrophy (SMA) in Adults and Children 2 Months and Older, Genentech Provides Update On Phase III Study Of Tecentriq In Combination With Paclitaxel For People With Metastatic Triple-Negative Breast Cancer, FDA Approves Genentechs Tecentriq plus Cotellic and Zelboraf for People With Advanced Melanoma, Genentech Provides an Update on the Phase III COVACTA Trial of Actemra in Hospitalized Patients With Severe COVID-19 Associated Pneumonia, Phase III Data Show Port Delivery System With Ranibizumab Enabled Over 98% of Patients to Go Six Months Between Treatments for Neovascular Age-Related Macular Degeneration, Genentech Provides Update on Phase III Study of Tecentriq in Women With Advanced-Stage Ovarian Cancer, New Data From Phase IIIb Study Reinforces Safety Profile of Genentechs Hemlibra (emicizumab-kxwh) in People With Hemophilia A, FDA Approves Genentechs Phesgo (Fixed-Dose Combination of Perjeta and Herceptin for Subcutaneous Injection) for HER2-Positive Breast Cancer, Genentechs IPATential150 Study Evaluating Ipatasertib in Combination With Abiraterone and Prednisone/Prednisolone Met One of Its Co-Primary Endpoints, Genentechs Tecentriq in Combination With Chemotherapy (Including Abraxane) Meets Primary Endpoint of Improved Pathological Complete Response, Regardless of PD-L1 Status, as Initial Treatment for People With Early Triple-negative Breast Cancer, Genentech Announces 2-Year Risdiplam Data From SUNFISH and New Data From JEWELFISH in Infants, Children and Adults With Spinal Muscular Atrophy (SMA), Positive Phase III Results for Venclexta Combination in Acute Myeloid Leukemia Presented at EHA 2020, FDA Approves Genentechs Tecentriq in Combination With Avastin for People With the Most Common Form of Liver Cancer, Genentech Initiates Phase III Clinical Trial of Actemra Plus Remdesivir in Hospitalized Patients With Severe COVID-19 Pneumonia, Port Delivery System With Ranibizumab Shows Positive Phase III Results in Neovascular Age-Related Macular Degeneration, New Longer-Term Data Reinforce Safety of Genentechs Satralizumab in Adults and Adolescents With Neuromyelitis Optica Spectrum Disorder (NMOSD), FDA Approves Genentechs Tecentriq as a First-Line Monotherapy for Certain People With Metastatic Non-Small Cell Lung Cancer, Genentech to Present First Clinical Data on Novel Anti-TIGIT Cancer Immunotherapy Tiragolumab at ASCO, Changes to the Roche Enlarged Corporate Executive Committee, New Data at the ASCO20 Virtual Scientific Program Reflects Genentechs Commitment to Accelerating Progress in Cancer Care, Genentechs Risdiplam Shows Significant Improvement in Survival and Motor Milestones in Infants With Type 1 Spinal Muscular Atrophy (SMA), New 6-Year Data for Genentechs Ocrevus (ocrelizumab) Show Earlier Treatment Initiation Nearly Halves Risk of Needing Walking Aid in Relapsing Multiple Sclerosis, FDA and EMA Accept Applications for Genentechs Ocrevus (ocrelizumab) Shorter 2-Hour Infusion Time, Genentech Provides Regulatory Update on Risdiplam for the Treatment of Spinal Muscular Atrophy (SMA), FDA Accepts Genentechs New Drug Application for Xofluza for the Treatment of Influenza In Children, Genentech Announces Venclexta Combination Improved Overall Survival in People With Previously Untreated Acute Myeloid Leukemia, Genentech Announces FDA Approval of Clinical Trial for Actemra to Treat Hospitalized Patients With Severe COVID-19 Pneumonia, Genentech Initiates Phase III Clinical Trial Of Actemra In Hospitalized Patients With Severe COVID-19 Pneumonia, FDA Grants Breakthrough Therapy Designation for Genentechs Esbriet (pirfenidone) in Unclassifiable Interstitial Lung Disease, FDA Accepts Genentechs Biologics License Application for Fixed-Dose Subcutaneous Combination of Perjeta And Herceptin For HER2-Positive Breast Cancer, FDA Grants Priority Review to Genentechs Tecentriq Monotherapy as First-Line Treatment of Certain People With Advanced Non-Small Cell Lung Cancer, Genentech Provides Topline Results From Investigator-Led Phase II/III Trial With Gantenerumab in Rare Inherited Form of Alzheimers Disease, Genentechs Risdiplam Showed Significant Improvement in Motor Function in People Aged 2-25 With Type 2 or 3 Spinal Muscular Atrophy, Genentech Submits Supplemental Biologics License Application to the FDA for Tecentriq in Combination With Avastin for the Most Common Form of Liver Cancer, Genentech Provides an Update on Phase III Study of Tecentriq in People With Muscle-Invasive Urothelial Cancer, Genentechs Risdiplam Meets Primary Endpoint in Pivotal FIREFISH Trial in Infants With Type 1 Spinal Muscular Atrophy, Genentech Announces Phase III Study Results for Tecentriq Plus Cotellic and Zelboraf in People With Previously Untreated BRAF V600 Mutation-positive Advanced Melanoma, Genentechs Fixed-dose Subcutaneous Combination of Perjeta and Herceptin Comparable to Intravenous Formulations in People With HER2-Positive Breast Cancer, FDA Accepts Supplemental Biologics License Application for Xolair (Omalizumab) for the Treatment of Nasal Polyps, New Data Demonstrate the Continued Clinical Benefit of Fixed-duration, Chemotherapy-free Venclexta-based Treatments in Chronic Lymphocytic Leukemia, Genentech Announces New Data on Novel CD20-CD3 Bispecific Cancer Immunotherapies in People With Difficult-to-Treat Lymphomas, FDA Approves Genentechs Tecentriq Plus Chemotherapy (Abraxane and Carboplatin) for The Initial Treatment of Metastatic Non-Squamous Non-Small Cell Lung Cancer, Positive Phase III Results for Genentechs Satralizumab in Neuromyelitis Optica Spectrum Disorder Published in the New England Journal of Medicine, FDA Grants Priority Review to Genentechs Risdiplam for Spinal Muscular Atrophy, Genentech Presents Pivotal Data Demonstrating Tecentriq in Combination With Avastin Improves Overall Survival in People With the Most Common Form of Liver Cancer, Genentech to Present New and Updated Data for Seven Approved and Investigational Medicines Across Multiple Types of Breast Cancer at the 2019 San Antonio Breast Cancer Symposium, Genentechs Risdiplam Meets Primary Endpoint In Pivotal SUNFISH Trial in People With Type 2 or 3 Spinal Muscular Atrophy, Genentechs Gazyva (obinutuzumab), in Combination With Standard of Care, More Than Doubles the Percentage of Lupus Nephritis Patients Achieving Complete Renal Response, Compared To Standard of Care Alone, Genentech to Present New Data Highlighting Breadth of Hematology Portfolio and Pipeline at the American Society of Hematology 2019 Annual Meeting, FDA Accepts Genentechs Biologics License Application for Satralizumab for Neuromyelitis Optica Spectrum Disorder, Genentechs Tecentriq in Combination With Avastin Increased Overall Survival and Progression-Free Survival in People With Unresectable Hepatocellular Carcinoma, Genentech Announces FDA Approval of Xofluza (Baloxavir Marboxil) for People at High Risk of Developing Influenza-Related Complications, Phase III PEMPHIX Study Shows Genentechs Rituxan (Rituximab) Superior to Mycophenolate Mofetil in Patients With Pemphigus Vulgaris, Genentech Presents Positive Phase III Results for Tecentriq (Atezolizumab) in Combination With Platinum-Based Chemotherapy in People With Previously Untreated Advanced Bladder Cancer, Genentech to Present Results of First Prospective Trial Using Blood-Based Next Generation Sequencing Which Successfully Identifies People for Treatment With Alecensa (Alectinib), Genentechs Tecentriq (Atezolizumab) Improves Overall Survival as a First-Line Monotherapy in Certain People With Advanced Non-Small Cell Lung Cancer, FDA Approves Genentechs Rituxan (Rituximab) in Children With Two Rare Blood Vessel Disorders, FDA Grants Breakthrough Therapy Designation for Genentechs Gazyva (Obinutuzumab) in Lupus Nephritis, Genentech Presents New Six-Year Ocrevus (Ocrelizumab) Data Which Showed That Earlier Initiation and Continuation of Treatment Reduced Disability Progression in Multiple Sclerosis, Genentechs Fixed Dose Subcutaneous Combination of Perjeta And Herceptin Showed Non-Inferiority When Compared to Intravenous Formulations for People With HER2-Positive Breast Cancer, Genentechs Tecentriq (Atezolizumab) as a First-Line Monotherapy Helped Certain People With Advanced Non-Small Cell Lung Cancer Live Longer Compared With Chemotherapy, Genentechs Satralizumab Significantly Reduced Relapse Risk in Second Positive Phase III Study for Neuromyelitis Optica Spectrum Disorder, Genentech Presents New Ocrevus (Ocrelizumab) Biomarker Data That Increase Understanding of Disease Progression in Multiple Sclerosis at ECTRIMS, Genentech to Present Pivotal Data for Satralizumab in Neuromyelitis Optica Spectrum Disorder and Six-Year Ocrevus (Ocrelizumab) Data in Multiple Sclerosis at ECTRIMS, Genentech Presents Positive Phase III Study Results for One-Dose Xofluza (Baloxavir Marboxil) in Children With the Flu, Positive Phase III Results Show Xofluza (Baloxavir Marboxil) Reduces Risk of Developing the Flu After Contact With an Infected Person by 86 Percent, FDA Approves Genentechs Rozlytrek (entrectinib) for People With ROS1-Positive, Metastatic Non-Small Cell Lung Cancer and NTRK Gene Fusion-Positive Solid Tumors, Genentechs Tecentriq (Atezolizumab) Plus Platinum-Based Chemotherapy Reduced the Risk of Disease Worsening or Death in People With Previously Untreated Advanced Bladder Cancer, Genentech Presents a Broad Range of Data for Hemlibra (Emicizumab-kxwh) Demonstrating Continued Benefits for People With Hemophilia A at the ISTH 2019 Congress, Genentech Announces Positive Results for First Global Phase III Study Investigating One-dose XOFLUZA (Baloxavir Marboxil) in Children With the Flu, Phase III PEMPHIX Study Showed That Genentechs Rituxan (Rituximab) is Superior to Standard of Care in Achieving Sustained Remission in Patients with Pemphigus Vulgaris, FDA Grants Priority Review to Genentechs Rituxan (Rituximab) in Children With Two Rare Blood Vessel Disorders, FDA Grants Genentechs Polivy Accelerated Approval for People With Previously Treated Aggressive Lymphoma, Genentechs Gazyva (Obinutuzumab) Delivers Positive Topline Results for Phase II Lupus Nephritis Study, Pivotal Phase III CLL14 Results for Venclexta in Combination With Gazyva for Chronic Lymphocytic Leukemia Presented at ASCO 2019 and Published in the New England Journal of Medicine, Phase III Study Showed XOFLUZA (Baloxavir Marboxil) is Effective at Preventing Influenza Infection, Xolair (omalizumab) Significantly Reduced Nasal Polyps and Congestion Symptoms in Adults With Chronic Rhinosinusitis With Nasal Polyps in Two Phase III Studies, Genentech Announces FDA Approval for Venclexta plus Gazyva for People With Previously Untreated Chronic Lymphocytic Leukemia, Genentechs Personalized Medicine Entrectinib Shrank Tumors Harboring NTRK, ROS1 Or ALK Gene Fusions in Children and Adolescents, Genentech to Present New Data Highlighting Comprehensive Approach to Cancer Care at 2019 American Society Of Clinical Oncology (ASCO) Annual Meeting, Genentech to Present New OCREVUS (ocrelizumab) Data Analyses Showing Significant Reduction of Disability Progression in Relapsing and Primary Progressive Multiple Sclerosis at the AAN Annual Meeting, Genentech Presents Data from the Risdiplam Pivotal FIREFISH and SUNFISH Studies in Spinal Muscular Atrophy at the 2019 AAN Annual Meeting, FDA Approves Genentech's Kadcyla for Adjuvant Treatment of People With HER2-Positive Early Breast Cancer With Residual Invasive Disease After Neoadjuvant Treatment, New Genentech Data at the 2019 AAN Annual Meeting Showcase Breadth and Promise of Neuroscience Portfolio, FDA Approves Genentechs Tecentriq in Combination With Chemotherapy for the Initial Treatment of Adults With Extensive-Stage Small Cell Lung Cancer, FDA Grants Genentechs Tecentriq in Combination With Abraxane Accelerated Approval for People With PD-L1-Positive, Metastatic Triple-Negative Breast Cancer, Genentech Submits Supplemental New Drug Application to FDA for Venclexta Plus Gazyva for Previously Untreated Chronic Lymphocytic Leukemia with Co-Existing Medical Conditions, FDA Accepts Genentechs Supplemental New Drug Application for Xofluza (baloxavir marboxil) for the Treatment of Influenza in People at High Risk of Complications, FDA Approves Herceptin Hylecta for Subcutaneous Injection in Certain HER2-Positive Breast Cancers, FDA Grants Priority Review to Genentechs Polatuzumab Vedotin in Previously Treated Aggressive Lymphoma, FDA Grants Priority Review to Genentechs Personalized Medicine Entrectinib, Genentech Submits Supplemental Biologics License Application to FDA For Kadcyla for Adjuvant Treatment of People With HER2-Positive Early Breast Cancer With Residual Disease After Neoadjuvant Treatment, Genentech to Discontinue Phase III CREAD 1 and 2 Clinical Studies of Crenezumab in Early Alzheimers Disease (AD) - Other Company Programs in AD Continue, FDA Accepts Genentechs Supplemental Biologics License Application for Tecentriq Plus Chemotherapy (Abraxane and Carboplatin) for the Initial Treatment of Metastatic Non-Squamous Non-Small Cell Lung Cancer, FDA Approves Genentechs Tecentriq in Combination With Avastin and Chemotherapy for the Initial Treatment of People With a Specific Type of Metastatic Lung Cancer, Genentechs Kadcyla Cut the Risk of Disease Recurring by Half Compared to Herceptin in People With HER2-Positive Early Breast Cancer With Residual Disease After Neoadjuvant Treatment, FDA Grants Priority Review to Genentechs Tecentriq in Combination With Chemotherapy for the Initial Treatment of Extensive-Stage Small Cell Lung Cancer, Genentechs Hemlibra (emicizumab-kxwh) Provided Sustained Bleed Control in the Largest Pivotal Study to Date of Children With Hemophilia A With Factor VIII Inhibitors, New Venclexta Data Demonstrate Deep Responses in Two of the Most Common Types of Leukemia, FDA Approves The ACTpen For Genentechs ACTEMRA, A Single-Dose, Prefilled Autoinjector For The Treatment Of Rheumatoid Arthritis, Giant Cell Arteritis And Two Forms Of Juvenile Arthritis, Genentech Announces FDA Grants Venclexta Accelerated Approval for People With Newly-Diagnosed Acute Myeloid Leukemia or Those Who Are Ineligible For Intensive Induction Chemotherapy, FDA Grants Priority Review to Genentechs Tecentriq in Combination With Abraxane for the Initial Treatment of People With PD-L1-Positive, Metastatic Triple-Negative Breast Cancer, Genentech to Present New Data From Its Industry-Leading Hematology Portfolio at the American Society of Hematology (ASH) 2018 Annual Meeting, Phase III Data Showed That Venclexta Plus Gazyva Reduced The Risk Of Disease Worsening Or Death In People With Previously Untreated Chronic Lymphocytic Leukemia With Co-Morbidities, New STAIRWAY Study Data Shows Potential for Extended Durability With Faricimab in Wet Age-Related Macular Degeneration (AMD), Genentech Announces FDA Approval of XOFLUZA (Baloxavir Marboxil) for Influenza, Genentechs Tecentriq Plus Chemotherapy (Carboplatin and Abraxane) as an Initial Treatment Helped People With Advanced Non-Squamous Non-Small Cell Lung Cancer Live Significantly Longer Compared to Chemotherapy Alone, Genentechs Investigational Personalized Medicine Entrectinib Shrank Tumors in People With NTRK Fusion-Positive Solid Tumors, Genentechs Tecentriq in Combination With Abraxane Improves Outcomes as an Initial Treatment for People With PD-L1-Positive Metastatic Triple-Negative Breast Cancer, FDA Approves Label Update for Genentechs Rituxan (Rituximab) in Two Rare Forms of Vasculitis, Genentechs Kadcyla Reduced the Risk of Disease Recurring in People With HER2-Positive Early Breast Cancer With Residual Disease After Neoadjuvant Treatment, OCREVUS (Ocrelizumab) Data Show Early Initiation of Treatment Reduces Disability Progression over Five Years in Relapsing and Primary Progressive Multiple Sclerosis, Genentech to Present New Positive Data from Its Broad Cancer Immunotherapy Program and Across a Wide Range of Cancers at The European Society for Medical Oncology (ESMO) 2018 Congress, FDA Approves Genentechs Hemlibra (Emicizumab-kxwh) for Hemophilia A Without Factor VIII Inhibitors, Genentech Announces New Data for Risdiplam in Spinal Muscular Atrophy (SMA) at the World Muscle Society Congress, Positive Phase III Results for Baloxavir Marboxil in People at High Risk of Complications From Influenza to be Presented at IDWeek 2018, Genentech to Present Five-Year OCREVUS (Ocrelizumab) Efficacy and Safety Data in Relapsing and Primary Progressive Multiple Sclerosis at ECTRIMS, FDA Approves Genentech's Xolair (Omalizumab) Prefilled Syringe Formulation, Genentechs TECENTRIQ in Combination With Chemotherapy Helped People Live Significantly Longer as an Initial Treatment for People With Extensive-Stage Small Cell Lung Cancer, Genentechs TECENTRIQ in Combination With Pemetrexed and Platinum-Based Chemotherapy Reduced the Risk of Disease Worsening or Death in a Type of Previously Untreated Advanced Lung Cancer, Genentechs Investigational Medicine Entrectinib Showed a Durable Response of More Than Two Years in People With a Specific Type of Lung Cancer, FDA Approves Subcutaneous Formulation of Actemra for Use in Active Systemic Juvenile Idiopathic Arthritis (SJIA), a Rare Form of Juvenile Arthritis, Genentech to Present New Data from Its Extensive Lung Cancer Program at the 2018 World Conference on Lung Cancer (WCLC), Positive Phase III Results for Genentechs HEMLIBRA (emicizumab-kxwh) for Hemophilia A Without Factor VIII Inhibitors Published in New England Journal of Medicine, FDA Grants Breakthrough Therapy Designation for Xolair (Omalizumab) for Food Allergies, Genentech Unveils Positive Phase II Results for the Port Delivery System with Ranibizumab (PDS), the First-Ever Eye Implant to Achieve Sustained Delivery of a Biologic Medicine to Treat People With Wet Age-Related Macular Degeneration (AMD), Genentech to Present New Data Demonstrating the Breadth and Depth of Its Alzheimers Program at the Upcoming Alzheimer's Association International Conference (AAIC), Genentechs TECENTRIQ in Combination With Pemetrexed and Platinum-Based Chemotherapy Reduced the Risk of Disease Worsening or Death in the Initial Treatment of People With Advanced Lung Cancer, FDA Grants Breakthrough Therapy Designation for Genentechs TECENTRIQ in Combination With Avastin as First-Line Treatment for Advanced or Metastatic Hepatocellular Carcinoma (HCC), Phase III CAPSTONE-2 Study Showed That Baloxavir Marboxil Reduced Symptoms in People at High Risk of Complications From the Flu, Genentech Announces Submission of Supplemental New Drug Application for Venclexta for People With Previously Untreated Acute Myeloid Leukemia who are Ineligible for Intensive Chemotherapy, Phase III IMpassion130 Study Showed Genentech's TECENTRIQ Plus Abraxane Significantly Reduced the Risk of Disease Worsening or Death in People With Metastatic or Locally Advanced Triple Negative Breast Cancer, FDA Grants Priority Review to Genentechs Baloxavir Marboxil for the Treatment of Influenza, Genentechs TECENTRIQ in Combination with Chemotherapy Helped People with Previously-Untreated Extensive-Stage Small Cell Lung Cancer Live Significantly Longer Compared to Chemotherapy, FDA Approves Genentechs Avastin (Bevacizumab) Plus Chemotherapy as a Treatment for Women With Advanced Ovarian Cancer Following Initial Surgery, Genentech Announces New Ocrevus (Ocrelizumab) Data on Long-Term Disability Benefits in Primary Progressive Multiple Sclerosis and Initiation of two Global Studies in Progressive MS, Genentech Announces FDA Approval for Venclexta Plus Rituxan for People With Previously Treated Chronic Lymphocytic Leukemia, FDA Approves Genentechs Rituxan (Rituximab) for Pemphigus Vulgaris, FDA Grants Priority Review to Genentechs HEMLIBRA (emicizumab-kxwh) for People With Hemophilia A Without Factor VIII Inhibitors, Phase III IMpower131 Study Showed Genentechs TECENTRIQ (Atezolizumab) Plus Chemotherapy (Carboplatin And ABRAXANE) Reduced the Risk of Disease Worsening or Death for People With Advanced Squamous Non-Small Cell Lung Cancer, Phase III IMpower130 Study Showed Genentechs TECENTRIQ (Atezolizumab) Plus Chemotherapy (Carboplatin and ABRAXANE) Helped People With Metastatic Non-Squamous Non-Small Cell Lung Cancer Live Significantly Longer Compared to Chemotherapy Alone, Genentechs HEMLIBRA (emicizumab-kxwh) Reduced Treated Bleeds by 96 Percent Compared to No Prophylaxis in Phase III Haven 3 Study in Hemophilia A Without Factor VIII Inhibitors, Follow-Up Phase III Data Showed Genentechs Alecensa Helped People With Alk-Positive Metastatic Non-Small Cell Lung Cancer Live A Median Of Almost Three Years Without Their Disease Worsening Or Death, Phase III IMpower150 Study Showed Genentech's TECENTRIQ and Avastin Plus Carboplatin and Paclitaxel Helped People With a Specific Type of Metastatic Lung Cancer Live Significantly Longer Compared to Avastin Plus Carboplatin and Paclitaxel, FDA Approves Subcutaneous Formulation of Actemra for use in Active Polyarticular Juvenile Idiopathic Arthritis (PJIA), a Rare Form of Juvenile Arthritis, Genentech to Present New Phase III Data for HEMLIBRA (emicizumab-kxwh) in People With Hemophilia A at the World Federation of Hemophilia 2018 World Congress, Genentech Provides Update on Phase III Study Of TECENTRIQ (Atezolizumab) and COTELLIC (Cobimetinib) in People With Heavily Pre-Treated Locally Advanced or Metastatic Colorectal Cancer, Genentech to Present New Data From Its Industry-Leading Oncology Portfolio at The 2018 American Society of Clinical Oncology (ASCO) Annual Meeting, FDA Grants Priority Review to Genentechs Cancer Immunotherapy TECENTRIQ (Atezolizumab) for Initial Treatment of People With a Specific Type of Metastatic Lung Cancer, New OCREVUS (Ocrelizumab) Data at AAN Demonstrate Significant Reductions in Disease Activity and Disability Progression in Relapsing Multiple Sclerosis, FDA Grants Breakthrough Therapy Designation For Genentechs HEMLIBRA (emicizumab-kxwh) in Hemophilia A Without Inhibitors, Genentech to Present New Data at AAN Highlighting Extensive Research for Ocrevus and Expanding Neuroscience Pipeline, Phase III IMpower150 Study Showed Genentechs TECENTRIQ (Atezolizumab) and Avastin (Bevacizumab) Plus Carboplatin and Paclitaxel Helped People With Advanced Lung Cancer Live Longer Compared to Avastin Plus Carboplatin and Paclitaxel, FDA Approves Genentechs Lucentis (Ranibizumab Injection) 0.3 mg Prefilled Syringe for Diabetic Macular Edema and Diabetic Retinopathy, Phase III IMpower131 Study Showed Genentechs TECENTRIQ (Atezolizumab) Plus Chemotherapy (Carboplatin and ABRAXANE) Reduced The Risk of Disease Worsening or Death in the Initial Treatment of People With a Type of Advanced Squamous Lung Cancer, FDA Grants Priority Review for Genentechs Rituxan (Rituximab) for Pemphigus Vulgaris, Phase II Data Support Potential for Novel Anti-VEGF/Anti-Angiopoietin-2 Bispecific Antibody, RG7716, for People With Diabetic Macular Edema, Phase III IMmotion151 Study Showed Genentechs TECENTRIQ (Atezolizumab) and Avastin (Bevacizumab) Reduced the Risk of Disease Worsening or Death by 26 Percent in Certain People with Advanced Kidney Cancer, FDA Approves Genentechs Perjeta (Pertuzumab) for Adjuvant Treatment of Specific Type of Early Breast Cancer, Genentech Announces Phase III Data Showing Venclexta plus Rituxan Reduced the Risk of Disease Progression or Death by 83 Percent Compared to a Standard of Care Regimen in Previously Treated Chronic Lymphocytic Leukemia, Phase II Data Showed Genentechs Investigational Polatuzumab Vedotin Plus Bendamustine and Rituxan (BR) Increased Complete Response Rates Compared to BR Alone in Previously Treated Aggressive Lymphoma, Phase III IMmotion151 Study Showed Genentechs Tecentriq (Atezolizumab) and Avastin (Bevacizumab) Reduced the Risk of Disease Worsening or Death for the Initial Treatment of Certain People with Advanced Kidney Cancer, Genentechs HEMLIBRA (emicizumab-kxwh) Continued to Substantially Reduce Bleeds in People with Hemophilia A with Inhibitors, Genentechs HEMLIBRA (emicizumab-kxwh) Every Four Weeks Controlled Bleeds in Phase III Study in Hemophilia A, Phase III IMpower150 Study Showed Tecentriq (atezolizumab) and Avastin (bevacizumab) Plus Chemotherapy Reduced the Risk of Disease Worsening or Death by 38 Percent for People with a Type of Advanced Lung Cancer, FDA Grants Genentechs Avastin Full Approval for Most Aggressive Form of Brain Cancer, First Cancer Screen Week Calls on Americans to Act Now Against Cancer by Taking Pledge to Get Screened, Phase III IMpower150 Study Showed Genentechs Tecentriq (Atezolizumab) and Avastin (Bevacizumab) Plus Chemotherapy Significantly Reduced the Risk of Disease Worsening or Death in the Initial Treatment of People with a Type of Advanced Lung Cancer, Genentechs Hemlibra (Emicizumab-kxwh) Significantly Reduced Bleeds in Phase III Study in Hemophilia A, FDA Approves Genentechs Hemlibra (Emicizumab-kxwh) for Hemophilia A with Inhibitors, FDA Approves Genentechs Gazyva for Previously Untreated Advanced Follicular Lymphoma, FDA Approves Zelboraf (Vemurafenib) for Erdheim-Chester Disease with BRAF V600 Mutation, FDA Approves Genentechs Alecensa (Alectinib) as First-Line Treatment for People with Specific Type of Lung Cancer, Genentech to Present New Data Across a Range of Blood Diseases at The American Society of Hematology (ASH) 2017 Annual Meeting, New OCREVUS (Ocrelizumab) Data at ECTRIMS Advance Clinical Understanding of Underlying Progression in Multiple Sclerosis, FDA Accepts Genentechs Supplemental Biologics License Application for Avastin as a Front-Line Treatment for Women with Advanced Ovarian Cancer, Genentech to Present New Ocrevus (Ocrelizumab) Efficacy & Safety Data in Relapsing and Primary Progressive Forms of Multiple Sclerosis at ECTRIMS, FDA Grants Priority Review for Genentechs Perjeta (Pertuzumab) for Adjuvant Treatment of HER2-Positive Early Breast Cancer, Phase III Data Showed That Venclexta Plus Rituxan Helped People With Previously Treated Chronic Lymphocytic Leukemia Live Longer Without Their Disease Worsening Compared to Bendamustine Plus Rituxan, Genentech Provides Update on First Lampalizumab Phase III Study for Geographic Atrophy, an Advanced Form of Age-Related Macular Degeneration, Genentech Issues Voluntary Nationwide Recall of Three Lots of Activase (Alteplase)-100 mg Due to Lack of Sterility Assurance of the Sterile Water for Injection, FDA Approves Genentechs Actemra (Tocilizumab) for the Treatment of CAR T Cell-Induced Cytokine Release Syndrome, FDA Grants Priority Review for Genentechs Gazyva in Previously Untreated Follicular Lymphoma, FDA Grants Priority Review to Genentech's Emicizumab for Hemophilia A with Inhibitors, FDA Grants Priority Review and Breakthrough Therapy Designation for Zelboraf (vemurafenib) in Erdheim-Chester Disease with BRAF V600 Mutation, FDA Grants Genentechs Alecensa Priority Review for Initial Treatment of People with ALK-Positive Lung Cancer, Positive Phase III Results of Genentechs Actemra (Tocilizumab) for the Treatment of Giant Cell Arteritis Published in New England Journal of Medicine, Positive Phase III Results for Genentechs Emicizumab in Hemophilia A Published in The New England Journal of Medicine, Genentechs Emicizumab Showed Positive Results in Phase III Studies (HAVEN 1 And HAVEN 2) in Hemophilia A With Inhibitors, FDA Approves Rituxan Hycela (Rituximab and Hyaluronidase Human) for Subcutaneous Injection in Certain Blood Cancers, New Data at EAN Show Genentechs Ocrevus (Ocrelizumab) Significantly Reduced Multiple Measures of Disease Progression in Relapsing and Primary Progressive Multiple Sclerosis, APHINITY Study Shows Genentechs Perjeta-Based Regimen Reduced the Risk of Invasive Cancer Returning Compared to Herceptin and Chemotherapy in HER2-Positive Early Breast Cancer, Phase III Study Showed Genentechs Alecensa (Alectinib) Reduced the Risk of Disease Progression or Death by More Than Half Versus Crizotinib as First-Line Treatment in a Specific Type of Lung Cancer, FDA Approves Genentechs Actemra (Tocilizumab) for Giant Cell Arteritis, Genentech to Present New Data on Personalized Medicines and Cancer Immunotherapies at the 2017 American Society of Clinical Oncology (ASCO) Annual Meeting, Genentech Provides Update on Phase III Study Of TECENTRIQ (Atezolizumab) In People With Previously Treated Advanced Bladder Cancer, New Data at AAN Reinforce Clinical Benefit of Genentechs Ocrevus (Ocrelizumab) for Relapsing and Primary Progressive Multiple Sclerosis, Genentech to Present New Data at AAN Reinforcing Efficacy And Safety of Newly FDA Approved Ocrevus (Ocrelizumab) in Two Types of Multiple Sclerosis, FDA Grants Genentechs Tecentriq (Atezolizumab) Accelerated Approval as Initial Treatment for Certain People with Advanced Bladder Cancer, FDA Approves Genentechs Lucentis (Ranibizumab Injection) for Diabetic Retinopathy, the Leading Cause of Blindness Among Working Age Adults in the United States, Genentech Announces Positive Interim Results for Emicizumab in Phase III Study of Children with Hemophilia A, Phase III Study Shows Genentechs Alecensa Was Superior to Crizotinib in a Specific Type of Lung Cancer, FDA Advisory Committee Unanimously Recommends Approval of Genentechs Subcutaneous Rituximab for Certain Blood Cancers, FDA Approves Genentechs OCREVUS (Ocrelizumab) For Relapsing and Primary Progressive Forms of Multiple Sclerosis, FDA Grants Breakthrough Therapy Designation for Rituxan (Rituximab) in Pemphigus Vulgaris, Phase III APHINITY Study Shows Genentechs Perjeta Regimen Helped People with an Aggressive Type of Early Breast Cancer Live Longer without their Disease Returning Compared to Herceptin and Chemotherapy, Phase II Study Supports Potential for Genentechs Tecentriq (Atezolizumab) Plus Avastin (Bevacizumab) for People with Locally Advanced or Metastatic Renal Cell Carcinoma, FDA Grants Priority Review For Genentechs Actemra (Tocilizumab) Supplemental Biologics License Application For Giant Cell Arteritis, a Form of Vasculitis, FDA Grants Genentechs Cancer Immunotherapy Tecentriq (Atezolizumab) Priority Review in Additional Type of Advanced Bladder Cancer, FDA Approves Genentechs Lucentis (Ranibizumab Injection) for Myopic Choroidal Neovascularization, Positive Phase III Results of Genentechs Investigational Medicine Ocrevus (Ocrelizumab) Published in New England Journal of Medicine, Genentechs Emicizumab for Hemophilia A Meets Primary Endpoint in Phase III Study, FDA Extends Review of Application for OCREVUS (Ocrelizumab), FDA Approves Genentechs Avastin (Bevacizumab) Plus Chemotherapy for a Specific Type of Advanced Ovarian Cancer, Genentechs Gazyva Helped People With Previously Untreated Follicular Lymphoma Live Significantly Longer without their Disease Worsening Compared to Rituxan, Phase III GiACTA Study Shows Genentechs Actemra, Genentech Showcases New Clinical Data Across a Variety of Blood Diseases at American Society of Hematology 2016 Annual Meeting, Genentech to Present New Data on Medicines for Autoimmune Diseases and Severe Inflammatory Disorders at the 2016 ACR/ARHP Annual Meeting, FDA Approves Genentechs Cancer Immunotherapy Tecentriq, FDA Grants Priority Review to Genentechs Lucentis, FDA Grants Breakthrough Therapy Designation for Genentechs Actemra (Tocilizumab) in Giant Cell Arteritis, a Form of Vasculitis, FDA Grants Breakthrough Therapy Designation for Genentechs Alecensa, Phase III Efficacy Results of Investigational Medicine Ocrevus (Ocrelizumab) Reinforced by Exploratory Analyses in Two Forms of Multiple Sclerosis, Phase III Study Showed Genentechs Cancer Immunotherapy TECENTRIQ, Genentech Provides Update on Phase III Study of Gazyva in People with Previously Untreated Diffuse Large B-Cell Lymphoma, FDA Grants Priority Review for Genentechs OCREVUS (Ocrelizumab) Biologics License Application, Genentechs Cancer Immunotherapy Tecentriq (atezolizumab) Shrank Tumors in People with Previously Untreated Advanced Bladder Cancer, Phase III Study Shows Genentechs Actemra, FDA Grants Genentechs Cancer Immunotherapy TECENTRIQ (atezolizumab) Accelerated Approval for People with a Specific Type of Advanced Bladder Cancer, Genentech Highlights Personalized Medicines and Cancer Immunotherapies at 2016 American Society of Clinical Oncology (ASCO) Annual Meeting, Genentech to Present New Data at AAN Showing Superior Efficacy of Investigational Medicine Ocrelizumab Versus Comparators on Disease Activity and Progression in Two Forms of Multiple Sclerosis, FDA Grants Priority Review for Genentechs Cancer Immunotherapy Atezolizumab in Specific Type of Lung Cancer, FDA Grants Genentechs Cancer Immunotherapy Atezolizumab Priority Review for Advanced Bladder Cancer, FDA Files Genentechs Supplemental Biologics License Application of Xolair, Genentech Provides Update on Two Identical Phase III Studies of Lebrikizumab in People with Severe Asthma, FDA Approves Genentechs Gazyva (Obinutuzumab) for Certain People with Previously Treated Follicular Lymphoma, FDA Grants Breakthrough Therapy Designation for Genentechs Investigational Medicine Ocrelizumab in Primary Progressive Multiple Sclerosis, FDA Grants Priority Review for Venetoclax New Drug Application, FDA Grants Genentechs Alecensa (Alectinib) Accelerated Approval for People with a Specific Type of Lung Cancer, Pivotal Phase II Study Showed Nearly 80 Percent of People with Hard-to-treat Type of Chronic Lymphocytic Leukemia Responded to Investigational Medicine Venetoclax, New Results from CLL11 Study Show Gazyva Provided People with Previously Untreated Chronic Lymphocytic Leukemia a Treatment-free Period of Nearly Four Years, Updated Data Showed That Cotellic (Cobimetinib) in Combination With Zelboraf (Vemurafenib) Helped People With a Specific Type of Advanced Melanoma Live Significantly Longer Than With Zelboraf Alone, FDA Approves Genentechs Cotellic (Cobimetinib) in Combination With Zelboraf (Vemurafenib) in Advanced Melanoma, Genentech to Present New Clinical Data Across a Variety of Blood Diseases at American Society of Hematology 2015 Annual Meeting, Genentechs Ocrelizumab First Investigational Medicine to Show Positive Pivotal Study Results in Both Relapsing and Primary Progressive Forms of Multiple Sclerosis, Genentechs Ocrelizumab First Investigational Medicine to Show Efficacy in People with Primary Progressive Multiple Sclerosis in Large Phase III Study, Genentech Presents Positive Results from Pivotal Study of Investigational Immunotherapy Atezolizumab in Specific Type of Advanced Bladder Cancer at 2015 European Cancer Congress, Two Positive Studies of Genentechs Investigational Cancer Immunotherapy Atezolizumab in Specific Type of Lung Cancer Presented at 2015 European Cancer Congress, FDA Grants Genentech's Alectinib Priority Review for Specific Type of ALK-Positive Lung Cancer, Genentech to Present Data from 15 Medicines Across Its Portfolio of Cancer Immunotherapy and Targeted Medicines During the 2015 European Cancer Congress, U.S. FDA Grants Breakthrough Therapy Designation for Genentech's Investigational Medicine ACE910 for People With Hemophilia A With Factor VIII Inhibitors, Pivotal Phase II Study Showed Genentechs Investigational Immunotherapy Atezolizumab Shrank Tumors in People with a Specific Type of Lung Cancer, Pivotal Phase II Study of Investigational Medicine Venetoclax Met Primary Endpoint in a Hard-To-Treat Type of Chronic Lymphocytic Leukemia, In a Pivotal Study, Genentechs Investigational Immunotherapy Atezolizumab Shrank Tumors in People With a Specific Type of Bladder Cancer, Genentechs ocrelizumab Significantly Reduced Both Relapses and Disability Progression versus interferon beta-1a (Rebif) in Two Phase III Studies in Multiple Sclerosis, FDA Grants Breakthrough Therapy Designation for Actemra (tocilizumab) in Systemic Sclerosis, Genentechs Perjeta Regimen Helped People with HER2-Positive Early Breast Cancer Live Longer without Their Disease Returning or Getting Worse Compared to Herceptin and Chemotherapy, Genentechs Gazyva Extended the Time People with Refractory Indolent Non-Hodgkins Lymphoma Lived Without Their Disease Worsening, Updated Data Showed Genentechs Investigational Combination of Cobimetinib and Zelboraf (Vemurafenib) Helps People With Advanced Melanoma Live for a Year Without Their Disease Worsening, Genentechs Investigational Medicine Alectinib Shrank Tumors in Nearly Half of People with Specific Type of Lung Cancer, Genentechs Investigational Immunotherapy MPDL3280A Reduced the Risk of Death by Half Compared with Chemotherapy in People with a Specific Type of Lung Cancer, Pivotal Data for Genentech Medicines in Lung and Blood Cancers To Be Presented at ASCO, Genentech Announces New STEM Education Initiative to Support South San Francisco Schools, Genentech Announces Plans To Expand Hillsboro Facility, FDA Grants Genentech's Cobimetinib Priority Review for Use in Combination with Zelboraf (Vemurafenib) in Advanced Melanoma, FDA Approves Genentechs Lucentis (Ranibizumab Injection) for Treatment of Diabetic Retinopathy in People with Diabetic Macular Edema, Genentechs Phase III Study of Gazyva Showed Significant Benefit in Refractory Indolent Non-Hodgkins Lymphoma, FDA Grants Breakthrough Therapy Designation for Genentechs Investigational Cancer Immunotherapy MPDL3280A (anti-PDL1) in Non-Small Cell Lung Cancer, neuroscience

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