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PANTHERx Rare Partnering with Gilead Sciences, Inc. for the Distribution of LIVDELZI

Aug 20, 2024
PANTHERx Rare, a leader in rare disease product patient access and support services in the United States, is pleased to announce it is partnering with Gilead Sciences, Inc. for the…
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Lilly opens state-of-the-art research and development center in the Boston Seaport

Aug 15, 2024
Eli Lilly and Company announced the opening of the Lilly Seaport Innovation Center (LSC), a research and development facility in the Boston Seaport dedicated to advancing Lilly's…
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Incyte and Syndax Announce FDA Approval of Niktimvo (axatilimab-csfr) for the Treatment of Chronic…

Aug 15, 2024
Incyte and Syndax Pharmaceuticals announced that the U.S. Food and Drug Administration (FDA) has approved Niktimvo (axatilimab-csfr), an anti-CSF-1R antibody, for the treatment of…
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Gilead’s Livdelzi (Seladelpar) Granted Accelerated Approval for Primary Biliary Cholangitis by FDA

Aug 15, 2024
Gilead Sciences, Inc. announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval for Livdelzi (seladelpar) for the treatment of primary biliary…
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Enhertu approved in China for patients with previously treated HER2-positive advanced or metastatic…

Aug 14, 2024
AstraZeneca and Daiichi Sankyo’s Enhertu (trastuzumab deruxtecan) has received conditional approval in China as a monotherapy for the treatment of adult patients with locally advanced…
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Replimune Announces First Patient Dosed in IGNYTE-3 Clinical Trial in Advanced Melanoma

Aug 14, 2024
Replimune Group, Inc., a clinical stage biotechnology company pioneering the development of a novel class of oncolytic immunotherapies, announced that the first patient has been…
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Pfizer Announces Top-Line Results of ABRYSVO for RSV in Immunocompromised Adults

Aug 13, 2024
Pfizer Inc. announced positive top-line safety and immunogenicity results from substudy B of the ongoing pivotal Phase 3 clinical trial ( NCT05842967 ) MONeT (RSV I Mmunizati ONStudy…
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FDA Approves YORVIPATH (Palopegteriparatide) as the First and Only Treatment for Hypoparathyroidism…

Aug 13, 2024
Ascendis Pharma A/S announced that the U.S. Food & Drug Administration (FDA) has approved YORVIPATH (palopegteriparatide; developed as TransCon PTH) for the treatment of…
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GSK’s Jemperli (dostarlimab) plus chemotherapy approved in Singapore as the first frontline…

Aug 7, 2024
GSK Singapore announced that the Singapore Health Sciences Authority (HSA) has approved a new indication for Jemperli (dostarlimab), which may now be used in combination with…
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Daiichi Sankyo and Merck Enter into Global Development and Commercialization Agreement for MK-6070

Aug 7, 2024
Daiichi Sankyo and Merck, known as MSD outside of the United States and Canada, have expanded their existing global co-development and co-commercialization agreement for three…
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