EC Approves Inrebic for Splenomegaly with Myelofibrosis 
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EC Approves Inrebic for Splenomegaly with Myelofibrosis 

On February 8, 2021, global biopharmaceutical company Bristol Myers Squibb shared that the European Commission (EC) approved a Marketing Authorization Application (MAA) for Inrebic (fedratinib). For around 10 years, there…

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SHR0302 for UC Met Trial Endpoints
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SHR0302 for UC Met Trial Endpoints

  Since its inception, biopharmaceutical company Reistone Biopharma Co. Ltd. ("Reistone") has worked to develop treatment options for patients with immuno-inflammatory and autoimmune conditions. Most recently, their drug candidate SHR0302,…

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NMPA Grants Conditional Approval to XOSPATA for FLT3mut+ AML
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NMPA Grants Conditional Approval to XOSPATA for FLT3mut+ AML

  In an early February press release, pharmaceutical company Astellas Pharma Inc. ("Astellas") shared that XOSPATA (gilteritinib) was given conditional approval in China for the treatment of patients with FLT3-mutated…

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