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Lilly Trial Shows Dual Therapy Benefits in Psoriatic Arthritis Patients

Jan 9, 2026
Eli Lilly and Company has reported positive topline results from its novel TOGETHER-PsA Phase 3b trial, demonstrating that the concomitant use of Taltz (ixekizumab) and Zepbound…
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Amgen Acquires Dark Blue to Advance Novel AML Treatments

Jan 9, 2026
Amgen has announced the acquisition of Dark Blue Therapeutics Ltd., a privately held biotechnology company based in the United Kingdom, in a deal valued at up to $840 million. The…
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FDA Approves New 2-Gram Fibryga Kit for Bleeding Care

Jan 9, 2026
Octapharma USA has received approval from the U.S. Food and Drug Administration for a new 2-gram presentation of Fibryga®, a human plasma-derived fibrinogen concentrate, expanding…
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GSK Phase III Trials Show Promise for Chronic Hepatitis B Therapy

Jan 9, 2026
GSK plc has reported positive results from two pivotal phase III clinical trials evaluating bepirovirsen, an investigational antisense oligonucleotide therapy for chronic hepatitis B…
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Takeda Expands Entyvio Options Through Halozyme Technology Partnership

Jan 9, 2026
Takeda Pharmaceutical Company has entered into a global collaboration and license agreement with Halozyme Therapeutics to use Halozyme’s proprietary ENHANZE® drug delivery technology…
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Lilly to Acquire Ventyx in $1.2 Billion Inflammation Deal

Jan 8, 2026
Eli Lilly and Company has agreed to acquire Ventyx Biosciences in an all-cash transaction valued at approximately $1.2 billion, strengthening Lilly’s pipeline in inflammation-driven…
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Day One Completes Acquisition of Mersana Therapeutics

Jan 8, 2026
Day One Biopharmaceuticals has completed its acquisition of Mersana Therapeutics, marking a significant expansion of its oncology pipeline and reinforcing its strategy to advance…
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FDA Grants Expedited Status to Protara’s Pediatric Lymphatic Malformation Therapy

Jan 7, 2026
Protara Therapeutics, Inc., a clinical-stage biotechnology company focused on cancer and rare diseases, has received multiple regulatory boosts from the U.S. Food and Drug…
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China Approves Zai Lab’s AUGTYRO for NTRK Fusion Solid Tumors

Jan 7, 2026
China’s drug regulator has expanded treatment options for patients with rare, genetically driven cancers by approving Zai Lab Limited’s AUGTYRO™ (repotrectinib) for adult patients with…
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FDA Issues Complete Response Letter for Outlook’s Wet AMD Therapy

Jan 6, 2026
Outlook Therapeutics has received a setback in its efforts to bring an FDA-approved bevacizumab treatment for retinal disease to the U.S. market. The company announced that the U.S.…
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Press Releases

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