Category News

ASCENT-03: Trodelvy Significantly Improves PFS in First-Line mTNBC Patients Ineligible for Checkpoint Inhibitors

Trodelvy Marks Breakthrough in First-Line mTNBC Treatment with Positive Phase 3 ASCENT-03 Results Gilead Sciences has announced encouraging topline results from its Phase 3 ASCENT-03 clinical trial evaluating Trodelvy® (sacituzumab govitecan-hziy) in a particularly challenging patient population: individuals newly diagnosed…

Read MoreASCENT-03: Trodelvy Significantly Improves PFS in First-Line mTNBC Patients Ineligible for Checkpoint Inhibitors

US FDA Grants Approval for Nucala (Mepolizumab) to Treat Adults with Chronic Obstructive Pulmonary Disease (COPD)

GSK’s Nucala (Mepolizumab) Receives US FDA Approval as Add-On Maintenance Treatment for Adults with Eosinophilic Phenotype COPD GSK has officially announced a significant milestone in the treatment of chronic obstructive pulmonary disease (COPD) with the recent approval of Nucala (mepolizumab)…

Read MoreUS FDA Grants Approval for Nucala (Mepolizumab) to Treat Adults with Chronic Obstructive Pulmonary Disease (COPD)

Linvoseltamab Combos Show Early Promise in Relapsed/Refractory Multiple Myeloma

Regeneron’s Linvoseltamab Combinations Show Strong Early Signals in Relapsed/Refractory Multiple Myeloma in Phase 1b Trial Regeneron Pharmaceuticals,has reported encouraging early findings from the ongoing Phase 1b LINKER-MM2 study, evaluating linvoseltamab in combination with either carfilzomib or bortezomib in patients with…

Read MoreLinvoseltamab Combos Show Early Promise in Relapsed/Refractory Multiple Myeloma

FDA Grants Approval to Roche’s Susvimo for Treatment of Diabetic Retinopathy

FDA Approves Roche’s Susvimo as the First and Only Continuous-Delivery Treatment for Diabetic Retinopathy, Offering Nine-Month Dosing Durability In a significant advancement for patients suffering from diabetic retinopathy (DR), the U.S. Food and Drug Administration (FDA) has approved Susvimo® (ranibizumab…

Read MoreFDA Grants Approval to Roche’s Susvimo for Treatment of Diabetic Retinopathy

FDA Advisory Committee Declines to Support Genentech’s Columvi Expansion Proposal

Roche’s Genentech Faces Setback as FDA Advisory Committee Rejects Columvi Expansion Proposal The U.S. Food and Drug Administration’s (FDA) Oncologic Drugs Advisory Committee (ODAC) delivered a significant blow to Genentech, a subsidiary of Roche, by voting overwhelmingly against the company’s…

Read MoreFDA Advisory Committee Declines to Support Genentech’s Columvi Expansion Proposal

Analyzing the Economic and Commercial Drivers of Health in Small Island Developing States

Charting a Healthier Future: A Comprehensive Analysis of Economic and Commercial Determinants of Health in Small Island Developing States A newly released technical paper by the World Health Organization (WHO) marks a pivotal advancement in the global response to noncommunicable…

Read MoreAnalyzing the Economic and Commercial Drivers of Health in Small Island Developing States

Alnylam Releases 2024 Corporate Responsibility Report Highlighting ESG Progress

Alnylam Pharmaceuticals Unveils 2024 Corporate Responsibility Report, Showcasing Impact Across ESG Pillars Alnylam Pharmaceuticals, the industry leader in RNA interference (RNAi) therapeutics, has published its 2024 Corporate Responsibility Report, reaffirming its commitment to science, sustainability, equity, and ethical business conduct.…

Read MoreAlnylam Releases 2024 Corporate Responsibility Report Highlighting ESG Progress