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FDA Approves Veklury (Remdesivir) for COVID-19 Treatment in Patients With Severe Renal Impairment,…

Jul 17, 2023
Gilead Sciences, Inc. announced that the U.S. Food and Drug Administration (FDA) approved a supplemental new drug application (sNDA) for the use of Veklury (remdesivir) in COVID-19…
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Exclusive interview with AstraZeneca on the future of oligonucleotide drug development

Jul 14, 2023
Given the resurgence of investment and investigation into oligonucleotides, the Oligonucleotide CMC & Analytical Development team did an exclusive interview with leading industry…
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European Medicines Agency Accepts Astellas’ Marketing Authorization Application for…

Jul 14, 2023
Astellas Pharma Inc. announced the European Medicines Agency (EMA) has accepted for regulatory review the company's marketing authorization application (MAA) for zolbetuximab, a…
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Gilead Partners with CHAI and Penta to Improve Treatment and Adherence Rates Among Children with HIV…

Jul 14, 2023
Gilead Sciences, Inc. is pleased to announce two public-private partnerships. The first will accelerate the development of an investigational dispersible pediatric formulation…
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 Entrada to receive $224 million upfront payment and $26 million equity investment

Jul 14, 2023
The oligonucleotide field is ever evolving at a rapid pace, as experts continue to optimize manufacturing processes, develop robust analytical methods, and ensure the quality and safety…
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InnoCare and ArriVent Announce Clinical Development Collaboration

Jul 13, 2023
InnoCare Pharma and ArriVent Biopharma announced a clinical development collaboration to evaluate the combination of InnoCare’s novel SHP2 (Src Homology 2 domain containing protein…
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TheracosBio Announces Commercial Availability of Brenzavvy (bexagliflozin) for the Treatment of…

Jul 13, 2023
TheracosBio announced that Brenzavvy (bexagliflozin), an FDA-approved oral sodium-glucose cotransporter 2 (SGLT2) inhibitor, is now available by prescription through the Mark Cuban Cost…
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BeiGene Announces FDA Acceptance of sNDA for Fifth BRUKINSA Indication

Jul 13, 2023
BeiGene, a global biotechnology company, today announced the U.S. Food and Drug Administration (FDA) has accepted for review the Company’s supplemental new drug application (sNDA) for…
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LianBio Announces Clinical Supply Agreement with AstraZeneca in China to Evaluate BBP-398 in…

Jul 12, 2023
LianBio, a biotechnology company dedicated to bringing innovative medicines to patients in China and other major Asian markets, announced a clinical supply agreement with AstraZeneca in…
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FDA approves expanded indication for Novartis Leqvio (inclisiran) to include treatment of adults…

Jul 12, 2023
Novartis announced today that the US Food and Drug Administration (FDA) has approved a label update for Leqvio (inclisiran) to enable earlier use in patients with elevated LDL-C who…
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Press Releases

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