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Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 2, 2020

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Junshi Biosciences provides updates on JS-108 and JS-006 studies

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FDA accepts IND for CERC-803 to treat leukocyte adhesion deficiency type II

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Phase III ACTIVATE trial of mitapivat in PK deficiency meets primary endpoint

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RS-5614 studied in investigator-initiated trial for severe COVID-19

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Combination enhances solid tumor immunotherapy

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Edesa initiates phase II/III study of EB-05 for hospitalized patients with COVID-19

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Investigator-initiated trial to study Carragelose nasal spray for COVID-19 prophylaxis

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Preliminary week 18 phase Ib/IIa data reported for HST-001 in androgenic alopecia

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Rafael Pharmaceuticals to launch phase II study of CPI-613 in clear cell sarcoma of soft tissue

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Agenus initiates phase II expansion of AGEN-1181 plus balstilimab in colon cancer

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DMC completes positive safety review of CYNKCOVID study

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Korea Research Institute of Bioscience and Biotechnology patents peptides for IBD

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New USP19 inhibitors described by Integral Health Holdings, Valo Early Discovery

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Aligos Therapeutics discovers STING agonists

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FDA grants accelerated approval to Gavreto for advanced or metastatic RET-altered thyroid cancers

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Prodrugs of TLR7 and TLR8 antagonists identified at Bristol Myers Squibb

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New JAK inhibitors patented by Vimalan Biosciences

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FDA approves Xolair to treat nasal polyps

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Hetlioz approved in U.S. for nighttime sleep disturbances in Smith-Magenis syndrome

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Investigators develop a swine model of abdominal aortic aneurysm

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Targovax reports phase I data on ONCOS-102 with pembrolizumab in advanced melanoma

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Novel rat models of doxorubicin-induced left ventricular dysfunction

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A-3907 targets bile acid transport in the intestine and kidney for treating NASH, fibrosis

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Ashvattha Therapeutics presents htHD-FXRa for treating hepatic and biliary disorders

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Akeso reports preliminary data on cadonilimab for MSI-H advanced solid tumors

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FDA clears IND for phase I study of DHOHD inhibitor RP-7214 for COVID-19

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NEPTUNE study of OV-101 for Angelman syndrome misses primary endpoint

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U.K. approval for Pfizer and BioNTech's COVID-19 mRNA vaccine BNT-162b2

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IND for phase I study of SSAO/VAP-1 inhibitor TT-01025 cleared in U.S.

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