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Articles published by Genentech
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Genentech’s Fenebrutinib Maintains Near-Complete Suppression of Disease Activity and Disability Progression for up to Two Years in People With Relapsing Multiple Sclerosis
May 30, 2025
From
Genentech
Via
Business Wire
Tickers
RHHBY
New Two-year Follow-up of Genentech’s Columvi Extends Overall Survival in Relapsed or Refractory Diffuse Large B-cell Lymphoma Patients
May 23, 2025
From
Genentech
Via
Business Wire
Tickers
RHHBY
FDA Approves Genentech’s Susvimo for Diabetic Retinopathy
May 22, 2025
From
Genentech
Via
Business Wire
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Genentech Provides Update on FDA Advisory Committee Meeting on Columvi Combination for People With Relapsed or Refractory Diffuse Large B-cell Lymphoma
May 20, 2025
From
Genentech
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Business Wire
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Ten-Year APHINITY Data Show Genentech’s Perjeta-based Regimen Reduced the Risk of Death by 17% in HER2-Positive Early-Stage Breast Cancer
May 13, 2025
From
Genentech
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Business Wire
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Roche and Genentech Announce New North Carolina Manufacturing Facility
May 12, 2025
From
Genentech
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Business Wire
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New England Journal of Medicine Publishes Phase III Data Showing Single-dose Xofluza Significantly Reduces Influenza Virus Transmission
April 25, 2025
From
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Genentech and Roche Present Novel Therapeutic and Diagnostic Advancements in Alzheimer’s at AD/PD 2025
April 03, 2025
From
Genentech
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Business Wire
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Genentech Provides Update on Phase III Ocrevus High Dose Study in People With Relapsing Multiple Sclerosis
April 02, 2025
From
Genentech
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FDA Accepts Supplemental Biologics License Application for Genentech’s Gazyva for the Treatment of Lupus Nephritis
March 05, 2025
From
Genentech
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Business Wire
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FDA Approves Genentech’s TNKase® in Acute Ischemic Stroke in Adults
March 03, 2025
From
Genentech
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Phase III Study Shows Xolair May Be More Effective With Fewer Side Effects Than Oral Immunotherapy for the Treatment of Food Allergies
March 02, 2025
From
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FDA Approves Genentech’s Evrysdi Tablet as First and Only Tablet for Spinal Muscular Atrophy (SMA)
February 12, 2025
From
Genentech
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Business Wire
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New England Journal of Medicine Publishes New Data for Genentech’s Gazyva Which Shows Superiority Over Standard Therapy in People With Active Lupus Nephritis
February 07, 2025
From
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Business Wire
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FDA Approves Genentech’s Susvimo as the First and Only Continuous Delivery Treatment for the Leading Cause of Diabetes-Related Blindness
February 04, 2025
From
Genentech
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Business Wire
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Genentech’s Itovebi Demonstrated Statistically Significant and Clinically Meaningful Overall Survival Benefit in a Certain Type of HR-Positive Advanced Breast Cancer
January 28, 2025
From
Genentech
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Business Wire
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Genentech’s Phase IIb Study of Prasinezumab Missed Primary Endpoint, but Suggests Possible Benefit in Early-Stage Parkinson’s Disease
December 19, 2024
From
Genentech
Via
Business Wire
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New and Updated Data for Genentech’s Fixed-Duration Columvi and Lunsumio at ASH 2024 Reinforce Their Potential to Improve Outcomes for People With Lymphoma
December 09, 2024
From
Genentech
Via
Business Wire
Tickers
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Five-Year Results Confirm Genentech’s Polivy Combination Therapy as New Standard of Care for Previously Untreated Aggressive Lymphoma
December 08, 2024
From
Genentech
Via
Business Wire
Tickers
RHHBY
FDA Accepts Supplemental Biologics License Application for Genentech’s Columvi Combination for People With Relapsed or Refractory Diffuse Large B-Cell Lymphoma
December 05, 2024
From
Genentech
Via
Business Wire
Tickers
RHHBY
Genentech Reports Update on Phase III SKYSCRAPER-01 Study Results
November 26, 2024
From
Genentech
Via
Business Wire
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Genentech to Present New and Encouraging Long-term Follow-up Data Across Broad Hematology Portfolio at ASH 2024
November 05, 2024
From
Genentech
Via
Business Wire
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New England Journal of Medicine Publishes Landmark Phase III Results for Genentech’s Itovebi, Showing More Than Doubling of Progression-Free Survival in Certain Type of HR-Positive Advanced Breast Cancer
October 30, 2024
From
Genentech
Via
Business Wire
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Genentech’s Vabysmo Improved Vision in Underrepresented Populations With Diabetic Macular Edema (DME) in a First-Of-Its-Kind Study
October 18, 2024
From
Genentech
Via
Business Wire
Tickers
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Majority of Children With Spinal Muscular Atrophy (SMA) Treated With Genentech’s Evrysdi Are Able to Sit, Stand and Walk Independently, Two-Year Data Demonstrate
October 14, 2024
From
Genentech
Via
Business Wire
Tickers
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FDA Approves Genentech’s Itovebi, a Targeted Treatment for Advanced Hormone Receptor-Positive, HER2-Negative Breast Cancer With a PIK3CA Mutation
October 10, 2024
From
Genentech
Via
Business Wire
Tickers
RHHBY
Positive Phase III Results for Genentech’s Gazyva Show Superiority to Standard Therapy Alone in People With Lupus Nephritis
September 26, 2024
From
Genentech
Via
Business Wire
Tickers
RHHBY
Positive Phase III Results Show Xofluza Significantly Reduces the Transmission of Influenza Viruses
September 19, 2024
From
Genentech
Via
Business Wire
Tickers
RHHBY
FDA Approves Ocrevus Zunovo™ as the First and Only Twice-a-Year 10-Minute Subcutaneous Injection for People With Relapsing and Progressive Multiple Sclerosis
September 13, 2024
From
Genentech
Via
Business Wire
Tickers
RHHBY
FDA Approves Genentech’s Tecentriq Hybreza, the First and Only Subcutaneous Anti-PD-(L)1 Cancer Immunotherapy
September 12, 2024
From
Genentech
Via
Business Wire
Tickers
RHHBY
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