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Biogen Launches Phase 3 Trial of Felzartamab for Primary Membranous Nephropathy

  • The Pharma Data
  • July 2, 2025

Biogen Launches Global Phase 3 PROMINENT Trial Evaluating Felzartamab in Primary Membranous Nephropathy Biogen Inc. (Nasdaq: BIIB) has announced the initiation of dosing in its global Phase 3 clinical trial,…

Read MoreBiogen Launches Phase 3 Trial of Felzartamab for Primary Membranous Nephropathy
  • Regulatory

Takeda’s GAMMAGARD LIQUID ERC Approved by FDA as First Ready-to-Use Low-IgA Immunoglobulin Therapy

  • The Pharma Data
  • July 2, 2025

Takeda Secures FDA Approval for GAMMAGARD LIQUID ERC, the First Ready-to-Use Liquid Immunoglobulin Therapy with Low IgA Content Takeda (TSE:4502/NYSE:TAK) announced today that the U.S. Food and Drug Administration (FDA)…

Read MoreTakeda’s GAMMAGARD LIQUID ERC Approved by FDA as First Ready-to-Use Low-IgA Immunoglobulin Therapy
  • Business

Merck Completes SpringWorks Acquisition to Boost Healthcare Growth

  • The Pharma Data
  • July 2, 2025

Merck Finalizes $3.4 Billion Acquisition of SpringWorks Therapeutics to Strengthen Rare Tumor Portfolio and Drive Sustainable Healthcare Growth Merck, a global leader in science and technology, today announced the successful…

Read MoreMerck Completes SpringWorks Acquisition to Boost Healthcare Growth
  • Regulatory

Vertex’s ALYFTREK® Approved in EU for Cystic Fibrosis Treatment

  • The Pharma Data
  • July 2, 2025

Vertex Gains EU Approval for ALYFTREK®, a Next-Generation CFTR Modulator for Cystic Fibrosis Patients Vertex Pharmaceuticals (Nasdaq: VRTX) announced today that the European Commission has granted marketing authorization for ALYFTREK®…

Read MoreVertex’s ALYFTREK® Approved in EU for Cystic Fibrosis Treatment
  • Press Releases

Riliprubart Receives Orphan Drug Designation in Japan for CIDP

  • The Pharma Data
  • July 2, 2025

Riliprubart Receives Orphan Drug Designation in Japan for Chronic Inflammatory Demyelinating Polyneuropathy Sanofi announced that Japan’s Ministry of Health, Labour and Welfare (MHLW) has granted orphan drug designation to riliprubart,…

Read MoreRiliprubart Receives Orphan Drug Designation in Japan for CIDP
  • Research

Amgen Reports Positive Phase 3 Results for Bemarituzumab in FGFR2b+ Gastric Cancer

  • The Pharma Data
  • July 2, 2025

Amgen Reports Positive Phase 3 Results for Bemarituzumab in FGFR2b+ Gastric Cancer, Marking Milestone in Targeted Therapy Amgen (NASDAQ:AMGN) has announced a significant breakthrough in the treatment of gastric and…

Read MoreAmgen Reports Positive Phase 3 Results for Bemarituzumab in FGFR2b+ Gastric Cancer
  • Press Releases

Strategic Leadership Changes Announced by Roche

  • The Pharma Data
  • July 2, 2025

Roche Announces Key Leadership Transitions Within Enlarged Corporate Executive Committee Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced significant changes to its leadership team, as two esteemed members of its…

Read MoreStrategic Leadership Changes Announced by Roche
  • Press ReleasesResearch

AbbVie to Acquire Capstan to Boost Immunology Innovation

  • The Pharma Data
  • July 2, 2025

AbbVie to Acquire Capstan Therapeutics to Advance In Vivo CAR-T for Autoimmune Diseases AbbVie and Capstan Therapeutics have announced a definitive agreement for AbbVie to acquire Capstan in a move…

Read MoreAbbVie to Acquire Capstan to Boost Immunology Innovation
  • Regulatory

FDA Reviews Allergan’s SKINVIVE PMA for Neck Appearance Improvement

  • The Pharma Data
  • July 2, 2025

FDA Accepts Allergan’s Application to Expand SKINVIVE by JUVÉDERM® for Neck Line Treatment Allergan Aesthetics, an AbbVie company (NYSE: ABBV), announced that the U.S. Food and Drug Administration (FDA) has…

Read MoreFDA Reviews Allergan’s SKINVIVE PMA for Neck Appearance Improvement
  • News

Evaluating the Risk of NAION in Patients Using Semaglutide Medications

  • The Pharma Data
  • June 28, 2025

WHO Issues Global Safety Alert Over Vision Loss Risk Linked to Semaglutide-Based Medications The World Health Organization (WHO) has issued a global safety communication directed at healthcare professionals and regulatory…

Read MoreEvaluating the Risk of NAION in Patients Using Semaglutide Medications
  • News

WHO Scientific Group Publishes Findings on COVID-19’s Origins

  • The Pharma Data
  • June 28, 2025

WHO Scientific Advisory Group Releases In-Depth Report on the Origins of COVID-19 Amid Ongoing Calls for Transparency and Global Cooperation The World Health Organization (WHO) has taken another step forward…

Read MoreWHO Scientific Group Publishes Findings on COVID-19’s Origins
CN Bio
  • News

WHO and Key Stakeholders Launch Disability Health Equity Partnership

  • The Pharma Data
  • June 28, 2025

WHO Launches Landmark Global Initiative to Advance Health Equity for Over 1.3 Billion People with Disabilities In a pivotal step toward realizing global health equity, the World Health Organization (WHO)…

Read MoreWHO and Key Stakeholders Launch Disability Health Equity Partnership
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