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European Commission approves expanded age indication for GSK’s Arexvy, the first respiratory…

Sep 2, 2024
GSK plc announced that the European Commission has authorised Arexvy (respiratory syncytial virus vaccine, recombinant adjuvanted) for active immunisation for the prevention of lower…
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Aptose Receives $10 Million Through a Facility Agreement with Hanmi; Negotiating Future…

Sep 2, 2024
Aptose Biosciences Inc., a clinical-stage precision oncology company developing tuspetinib, a highly differentiated oral kinase inhibitor for the treatment of patients with acute…
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Lilly releases Zepbound (tirzepatide) single-dose vials, expanding supply and access for adults…

Aug 28, 2024
Eli Lilly and Company announced Zepbound (tirzepatide) 2.5 mg and 5 mg single-dose vials are available for self-pay for patients with an on-label prescription, significantly expanding…
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EC Approves Astellas’ PADCEVTM (enfortumab vedotin) in Combination with KEYTRUDA (pembrolizumab) for…

Aug 28, 2024
Astellas Pharma Inc. announced that the European Commission has granted Marketing Authorization for PADCEVTM (enfortumab vedotin, an antibody-drug conjugate ) in combination with…
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Pfizer Launches PfizerForAll, a Digital Platform that Helps Simplify Access to Healthcare

Aug 28, 2024
Pfizer Inc. introduced PfizerForAll , a user-friendly digital platform designed to make access to healthcare and managing health and wellness more seamless for people across the U.S.…
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Roche’s PiaSky approved in the EU as the first monthly subcutaneous treatment for people with PNH

Aug 27, 2024
Roche announced that the European Commission has approved PiaSky (crovalimab), a novel recycling monoclonal antibody that inhibits the complement protein C5, for adults and adolescents…
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UCB to Accelerate Innovation and Strategic Partnerships, Divesting Mature Product Portfolio in China

Aug 27, 2024
UCB, a global biopharmaceutical company, announced a strategic divestment deal in China, underscoring its strategic shift towards innovation and partnership in one of the world’s…
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BeiGene’s BGB-16673 Receives FDA Fast Track Designation for CLL/SLL

Aug 27, 2024
BeiGene, Ltd. announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track Designation to BGB-16673, an orally available investigational Bruton’s tyrosine kinase…
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Achieving Affordable Individualized Vaccines for Cancer Patients Faster

Aug 23, 2024
As BioNTech, Moderna, and Merck have recently released positive phase II clinical results for personalized cancer vaccines, the whole industry is now racing to develop affordable and…
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Achieving Clinical Success with Safe & Efficacious TGF-B Therapies

Aug 23, 2024
The race for clinical approval of TGF-β therapies is heating up, fueled by significant investments like Corbus Pharmaceuticals' recent $98.5 million and Biacara Therapeutics' $165…
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