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Arbutus Biopharma, X-Chem and Proteros biostructures Achieve First Milestone Under COVID-19…

Dec 8, 2021
Arbutus Biopharma Corporation, X-Chem, Inc. (X-Chem) and Proteros biostructures GmbH (Proteros) announced that Arbutus Biopharma has identified several molecules that inhibit the…
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Telix and NUCLIBER Sign Distribution Agreement for Prostate Cancer Imaging in Spain

Dec 8, 2021
Telix Pharmaceuticals Limited announces that it has entered into an exclusive commercial distribution agreement with Madrid-based NUCLIBER S.A. Spain (NUCLIBER) for Telix’s prostate…
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CP-COV03, a niclosamide-based oral antiviral drug, under study as possible cure for COVID-19…

Dec 8, 2021
Experimental results have been published for the first time showing that an antiviral drug containing niclosamide, an anthelmintic, in combination with dexamethasone, an…
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AstraZeneca and Ionis sign deal to develop and commercialise eplontersen

Dec 8, 2021
AstraZeneca has entered into a new global development and commercialisation agreement with Ionis Pharmaceuticals, Inc. (Ionis) for eplontersen, formerly known as IONIS-TTR-LRX. …
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Alvotech and Oaktree Acquisition Corp. II Announce Merger Agreement to Create a Leading…

Dec 8, 2021
-      Alvotech is a leading pure play biosimilar platform focused on the development and manufacture of high-quality biosimilar medicines for global markets.…
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Recursion and Bayer Expand Fibrosis Collaboration to Include Inferential Search Capabilities

Dec 7, 2021
Recursion a clinical-stage biotechnology company decoding biology to radically improve lives by industrializing drug discovery, development and beyond through disruptive innovation,…
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Gritstone bio and CEPI Expand Vaccine Agreement to Tackle Omicron Variant

Dec 7, 2021
Gritstone bio, Inc., a clinical-stage biotechnology company developing next generation cancer and infectious disease immunotherapies, and CEPI, the Coalition for Epidemic Preparedness…
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EMA accepts regulatory submission for olipudase alfa, the first potential therapy for ASMD

Dec 6, 2021
The European Medicines Agency (EMA) has accepted for review under an accelerated assessment procedure the Marketing Authorization Application (MAA) for olipudase alfa, Sanofi’s…
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FDA Approves Merck’s KEYTRUDA (pembrolizumab) as Adjuvant Treatment for Adult and Pediatric (≥12…

Dec 6, 2021
Merck, known as MSD outside the United States and Canada, announced that the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA, Merck’s anti-PD-1 therapy, for the adjuvant…
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Merck Announces Pause in Enrollment for Two Phase 3 Clinical Trials of Investigational,…

Dec 6, 2021
Merck, known as MSD outside the United States and Canada, announced a pause in enrollment for the IMPOWER 22 (MK-8591-022) and IMPOWER 24 (MK-8591-024) Phase 3 clinical studies…
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