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ImmunityBio Announces $320 Million Investment by Oberland Capital, with $210 Million Funded at…

Jan 3, 2024
ImmunityBio, Inc., a clinical-stage immunotherapy company announced an up to $320 million royalty financing and equity investment in the Company by Oberland Capital, with $210 million…
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MediLink Therapeutics Announces Worldwide Collaboration and License Agreement with Roche to develop…

Jan 3, 2024
MediLink Therapeutics ("MediLink"), announced that it has entered into a worldwide collaboration and license agreement with Roche on the development of a next-generation antibody-drug…
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European Medicines Agency Validates Bristol Myers Squibb’s Application for Repotrectinib for the…

Jan 3, 2024
Bristol Myers Squibb announced that the European Medicines Agency (EMA) has validated its marketing authorization application for the next-generation tyrosine kinase inhibitor (TKI)…
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Elpiscience and Astellas Enter into Research Collaboration and License Agreement for Novel…

Jan 3, 2024
Elpiscience Biopharma, Ltd. and Astellas Pharma Inc. announced a research collaboration and license agreement for novel bi-specific macrophage engagers, ES019 and another program. The…
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GSK enters exclusive license agreement with Hansoh for HS-20093

Dec 21, 2023
GSK plc and Hansoh Pharma, a Chinese biopharmaceutical company committed to discovering and developing life-changing medicines to help patients conquer serious diseases and disorders,…
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Ocelot Bio Receives FDA Orphan Drug Designation for OCE-205 for the Treatment of Ascites

Dec 21, 2023
Ocelot Bio, Inc., a clinical-stage biopharmaceutical company focused on the development of innovative therapeutics to treat complications of end-stage liver disease (ESLD), announced…
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Calliditas Therapeutics announces full FDA approval of TARPEYO, the only FDA-approved treatment for…

Dec 20, 2023
Calliditas Therapeutics AB announced that the U.S. Food and Drug Administration (FDA) has approved TARPEYO (budesonide) delayed release capsules to reduce the loss of kidney…
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FDA grants priority review to Xolair (omalizumab) for children and adults with food allergies based…

Dec 20, 2023
Roche announced that the U.S. Food and Drug Administration (FDA) has accepted, under Priority Review, the company’s supplemental Biologics License Application (sBLA) for Xolair…
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FDA Grants Priority Review to Merck’s New Biologics License Application for V116, an…

Dec 20, 2023
Merck, known as MSD outside of the United States and Canada, announced the U.S. Food and Drug Administration (FDA) has accepted for priority review a new Biologics License Application…
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Gilead and Compugen Announce Exclusive License Agreement for Novel Pre-Clinical Immunotherapy…

Dec 19, 2023
Gilead Sciences, Inc. announced an agreement with Compugen Ltd., a clinical-stage cancer immunotherapy company and a pioneer in computational target discovery, headquartered in Holon,…
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Industry Reports

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Press Releases

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