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South Korean Biotech Platforms Drive Surge in Multibillion-Dollar Global Licensing Deals

Monday, November 17, 2025

South Korean biotech firms accelerate global expansion with recordsetting licensing deals highlighting the regions rising competitiveness in drug development and platform innovation

China’s Groundbreaking Dual-Track Drug Reimbursement Reform Ushers in New Era for Pharma Market Access

Friday, November 14, 2025

China introduces a dualtrack reimbursement system for innovative drugs offering new access channels for global pharma manufacturers

Numab Therapeutics Enters into Agreement with Kaken Pharmaceutical for Multispecific Antibody NM81 in Inflammatory Bowel Disease

Friday, November 14, 2025

Numab Therapeutics and Kaken Pharmaceutical have entered into a new licence and codevelopment agreement to advance NM a multispecific antibody being developed for inflammatory bowel disease IBD

Kura Oncology and Kyowa Kirin Receive Approval for KOMZIFTI™ (ziftomenib for Relapsed or Refractory NPM1-Mutated AML

Friday, November 14, 2025

Kura Oncology and Kyowa Kirin have received full approval from the US Food and Drug Administration FDA for KOMZIFTI ziftomenib a oncedaily oral therapy for adults with relapsed or refractory acute myeloid leukaemia AML

Ascletis Announces Co-formulation of ASC36, Once-Monthly Next-Generation Amylin Receptor Agonist and ASC35, Once-Monthly Next-Generation GLP-1R/GIPR Dual Agonist for Clinical Development

Thursday, November 13, 2025

Ascletis Pharma announces a major advance in GLPRGIPR and amylin receptor agonist coformulation targeting nextstage clinical development using its proprietary peptide technologies

Parabilis Medicines Receives FDA Fast Track Designation for FOG-001 in Desmoid Tumours

Thursday, November 13, 2025

Parabilis Medicines has received Fast Track designation from the United States Food and Drug Administration FDA for FOG a firstinclass investigational therapy designed to treat desmoid tumours

Chiesi Group Enters into Agreement with Aliada Therapeutics to Advance Blood-Brain Barrier-Crossing Technology for Lysosomal Storage Disorders

Thursday, November 13, 2025

Chiesi Group has entered into an exclusive licence agreement with Aliada Therapeutics to progress bloodbrain barrier BBBcrossing platform technology aimed at treating lysosomal storage disorders LSDs

March Biosciences Receives FDA RMAT Designation for MB-105 in Relapsed/Refractory CD5-Positive T-Cell Lymphoma

Wednesday, November 12, 2025

March Biosciences has received Regenerative Medicine Advanced Therapy RMAT designation from the US Food and Drug Administration FDA for its lead candidate MB

Shilpa Pharma Lifesciences Awarded EcoVadis Gold Medal for Outstanding Sustainability Practices

Tuesday, November 11, 2025

Shilpa Pharma Lifesciences receives the prestigious EcoVadis Gold Medal recognizing its excellence in sustainability within global pharmaceutical manufacturing

Novartis Expands Radioligand Therapy Manufacturing with New Facility in California

Tuesday, November 11, 2025

Novartis has opened a new squarefoot radioligand therapy RLT manufacturing facility in Carlsbad California marking a major step in its US expansion strategy