Shares of Kodiak Sciences plunged in trading on February 23 after the company announced its Phase II/III study of a novel antibody biopolymer conjugate failed to hit the mark in treatment-naïve subjects with neovascular (wet) age-related macular degeneration.
The latest results from Genentech’s proposed eye disease treatments are demonstrating strong potential to help reduce treatment frequencies and deliver improved outcomes.
AbbVie is partnering with biotechnology firm REGENXBIO to develop and commercialize a new drug that could treat a wide range of eye diseases, including wet age-related macular degeneration (wet AMD).
Roche announced topline data from two identical Phase III trials (TENAYA and LUCERNE) of faricimab in neovascular or “wet” age-related macular degeneration (nAMD), with both studies hitting their primary endpoint.
Calithera Biosciences reported that the company’s CANTATA clinical trial of telaglenastat in patients with advanced or metastatic renal cell carcinoma (RCC) failed to hit the primary endpoint.
AVEO Oncology Announces Submission of New Drug Application to U.S. FDA for Tivozanib in Patients with Relapsed or Refractory Renal Cell Carcinoma
FDA, FDA/Regulatory, Immunotherapy, New Drug Application Submission, Renal Cell Carcinoma (RCC), Tyrosine kinase inhibitors, Vascular Endothelial Growth Factor (VEGF) InhibitorsAVEO Oncology submitted a New Drug Application to the U.S. Food and Drug Administration for tivozanib, the company’s vascular endothelial growth factor receptor tyrosine kinase inhibitor, as a treatment for relapsed or refractory renal cell carcinoma (RCC).
AstraZeneca and Merck’s Combo Therapy Flunks Late-Stage Ovarian Cancer Trial
BRCA mutation, Business, Clinical Trials, Collaborations, Combination Therapies, DNA Damage Response (DDR), National Cancer Institute, NRG Oncology, PARP Inhibitors, Platinum-Sensitive Relapsed Ovarian Cancer, R&D, Vascular Endothelial Growth Factor (VEGF) InhibitorsAstraZeneca and Merck announced that the Phase III GY004 trial of cediranib in combination with Lynparza compared to platinum-based chemotherapy in platinum-sensitive relapsed ovarian cancer failed to meet the primary endpoint.
FDA Approves Eylea for Diabetic Retinopathy
Approvals, Diabetic Macular Edema, Diabetic Retinopathy, Diabetics, FDA, FDA/Regulatory, New Indications, Supplemental Biologics License Application (sBLA), Vascular Endothelial Growth Factor (VEGF) Inhibitors, Vision Loss, Wet Age-Related Macular DegenerationThe U.S. FDA approved Regeneron Pharmaceuticals Inc.’s Eylea (aflibercept) Injection for all stages of diabetic retinopathy, which is the leading cause of vision loss in diabetic patients.
Days after rejecting Regeneron’s attempt to secure a supplemental approval for Eylea, the FDA approved a new dosing label for the drug in wet age-related macular degeneration (wet AMD).
Special Feature – Pharma Innovators: Paying attention to the innovators
AMD, Antidepressants, August 2017, Business, Company Launches, Consumers, Diabetic Gastroparesis, Healthcare Communications Agencies, Healthcare Communications Networks, Launches, Med Ad News, Migraine, Pharma, Pharma Leaders of Innovation special feature, Product Pipelines, Science, Vascular Endothelial Growth Factor (VEGF) InhibitorsTwo have been around in the pharmaceutical industry for a long time, and one is a relative newcomer. In considering this year’s pharma innovators to profile, the results of their accomplishments, not how long they have been around, steered the direction of this feature. Donna Murphy, global CEO of the recently formed agency network Havas Health & You; Abraham Gutman, president and CEO of AG Mednet; and C. David Nicholson, executive VP and chief R&D officer of Allergan, are being saluted for bringing new innovations to the fields of pharmaceutical advertising, clinical trial imaging and R&D, and their accomplishments are expected to echo into the future.