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Imjudo (tremelimumab) in combination with Imfinzi approved in the US for patients with unresectable…

Oct 25, 2022
AstraZeneca’s Imjudo (tremelimumab) in combination with Imfinzi (durvalumab) has been approved in the US for the treatment of adult patients with unresectable hepatocellular carcinoma…
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Astellas and Taysha Gene Therapies Announce Strategic Investment to Support Development of…

Oct 25, 2022
Astellas Pharma Inc. and Taysha Gene Therapies, Inc. announced a strategic investment to support the advancement of Taysha's adeno-associated virus (AAV) gene therapy development…
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Registration is now open for RNA Therapeutics Conference 2023

Oct 25, 2022
SAE Media Group reports: The 14th Annual RNA Therapeutics Conference is set to return in February 2023 with a key focus on mRNA therapeutic applications. SAE Media Group is delighted…
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Quizartinib Granted Priority Review in the U.S. for Patients with Newly Diagnosed FLT3-ITD Positive…

Oct 24, 2022
Daiichi Sankyo received notification of acceptance by the U.S. Food and Drug Administration (FDA) of the New Drug Application (NDA) of quizartinib in combination with standard…
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Kite and Refuge Biotechnologies Announce Exclusive License Agreement for Investigational Gene…

Oct 24, 2022
Kite, a Gilead Company and Refuge Biotechnologies, Inc. announced that Kite has entered into an exclusive, worldwide license agreement with Refuge, a synthetic biology company for…
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ARS Pharmaceuticals Announces FDA Acceptance of NDA for neffy (epinephrine nasal spray) for the…

Oct 24, 2022
ARS Pharmaceuticals, Inc. announced today that the U.S. Food and Drug Administration (FDA) has accepted for review ARS’ New Drug Application (NDA) for neffy for the emergency treatment…
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Sumitovant Biopharma, Sumitomo Pharma, and Myovant Sciences Enter into Definitive Agreement

Oct 24, 2022
Sumitovant Biopharma Ltd. in conjunction with parent company Sumitomo Pharma Co., Ltd. and Myovant Sciences announced today that they have entered into a definitive agreement pursuant…
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RINVOQ (Upadacitinib) Receives Its Sixth U.S. FDA Approval

Oct 24, 2022
AbbVie announces that the U.S. Food and Drug Administration (FDA) has approved RINVOQ (upadacitinib 15 mg, once daily), an oral therapy, for the treatment of adults with active…
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HOOKIPA announces strategic collaboration and license agreement with Roche to develop novel…

Oct 24, 2022
HOOKIPA Pharma Inc. a company developing a new class of immunotherapies based on its proprietary arenavirus platform, announced a strategic collaboration and license agreement with…
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Corium and Gurnet Point Capital Announce Manufacturing Business Acquisition and a $100 Million…

Oct 21, 2022
Corium, LLC a commercial-stage biopharmaceutical company leading the development and commercialization of novel neuroscience therapies, and Gurnet Point Capital (“Gurnet Point”), a…
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Press Releases

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