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BioWorld - Wednesday, December 17, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 28, 2017

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AAV-mediated liver delivery of secretable GAA improves long-term survival in Pompe disease mice

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Tasigna receives approval in Japan for treatment of pediatric chronic myeloid leukemia

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SK Chemicals launches SKYZoster shingles vaccine in South Korea

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Pfizer enrolling participants in phase I study of PF-06863135

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Clover Biopharmaceuticals receives approval to initiate clinical trials of SCB-808 in China

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FDA accepts NDA for OTX-101

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Maruho and RaQualia enter worldwide license agreement

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Celgene researchers report compounds with antiprotozoal activity

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Agents for the treatment of malaria described in Celgene patent

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P2X7 receptor antagonists for pain reported in Shionogi patent

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Beijing Jacobio Pharmaceuticals patents SHP-2 inhibitors

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Pramana Pharmaceuticals patent describes glucose-dependent insulinotropic receptor agonists

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Lilly initiates phase II study of LY-3002813 and LY-3202626 in early symptomatic Alzheimer's disease

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Athenex receives U.K. promising innovative medicine designation for Oraxol

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Combination therapy with gedatolisib shows promising preliminary antitumor activity in breast cancer

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Kaiso as a potential new biomarker and therapeutic target in TNBC

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NeuroRx enters agreement for clinical trial of NRX-100/NRX-101 regimen

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Phase II data show safety of combining Ra-223 with hormonal therapy and denosumab

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Phase III SIERRA study of Iomab-B cleared to continue enrollment

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Phase II safety data for abemaciclib as treatment of brain metastases secondary to HR+ breast cancer

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First patient enrolled in phase III OVAL study of VBL Therapeutics' VB-111

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Keytruda approved for new indication in Japan

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Innovation Pharmaceuticals reports preliminary data from phase IIa study of Kevetrin

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Protalix Biotherapeutics' pegunigalsidase alfa granted orphan drug status in E.U.

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New phase III trial explores use of TSC in newly diagnosed GBM

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CFDA designates lenvatinib for priority review and approval for HCC

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Bayer initiates phase III studies in Japan of molidustat in nondialysis patients with renal anemia

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Eli Lilly's Zyprexa approved for chemotherapy-induced nausea and vomiting in Japan

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