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Pfizer and BioNTech Submit Application to FDA for Emergency Use Authorization of Omicron…

Sep 27, 2022
Pfizer Inc. and BioNTech SE announced they have completed a submission to the U.S. Food and Drug Administration (FDA) requesting Emergency Use Authorization (EUA) of a 10-µg booster…
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Seagen and LAVA Therapeutics Announce Exclusive Worldwide License Agreement to Advance LAVA-1223

Sep 27, 2022
Seagen Inc. and LAVA Therapeutics N.V. announced an exclusive license agreement in which Seagen will work to develop, manufacture and commercialize LAVA-1223. LAVA-1223 is an advanced…
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Emergent BioSolutions Completes Acquisition of Exclusive Worldwide Rights to TEMBEXA…

Sep 27, 2022
Emergent BioSolutions Inc. announced that it has completed its acquisition of exclusive worldwide rights to TEMBEXA (brincidofovir), the first oral antiviral approved by the U.S. Food…
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Co-chairs invitation to attend the Pharmaceutical Cleanrooms Conference in London, UK

Sep 26, 2022
SAE Media Group reports: Conference co-chairs invite you to attend the 2nd Annual Next Generation Pharmaceutical Cleanrooms this October 2022. The conference will be co-chaired…
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Lynparza approved in China as 1st-line maintenance treatment with bevacizumab for HRD-positive…

Sep 26, 2022
AstraZeneca and MSD’s Lynparza (olaparib) has been approved in China for the maintenance treatment of adult patients with advanced epithelial ovarian, fallopian tube or primary…
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Massive Bio Continues to Grow in Europe

Sep 26, 2022
Massive Bio, which uses its proprietary artificial intelligence-based platform to match cancer patients to clinical trials regardless of where they live or their financial…
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U.S. District Court Rules In Favor of Merck in Sitagliptin Phosphate Patent Lawsuit

Sep 26, 2022
Merck, known as MSD outside of the United States and Canada, announced that the U.S. District Court for the Northern District of West Virginia ruled in favor of the company in a patent…
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Ultomiris approved in Europe for the treatment of adults with generalised myasthenia gravis

Sep 26, 2022
Ultomiris (ravulizumab) has been approved in Europe as an add-on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gMG) who are…
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GSK and Spero Therapeutics announce exclusive licence agreement for tebipenem HBr

Sep 23, 2022
GSK plc and Spero Therapeutics, Inc. announced they have entered into an exclusive licence agreement for tebipenem pivoxil hydrobromide (tebipenem HBr), a late-stage antibiotic being…
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Pfizer to Supply Global Fund Up to 6 Million PAXLOVID Treatment Courses for Low-and-Middle-Income…

Sep 23, 2022
Pfizer Inc. announced an agreement to supply up to six million treatment courses of its COVID-19 oral treatment, PAXLOVID (nirmatrelvir tablets and ritonavir tablets) to Global Fund as…
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Press Releases

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