Jessica Lynn has an educational background in writing and marketing. She firmly believes in the power of writing in amplifying voices, and looks forward to doing so for the rare disease community.

    Results Available from GS030 Study for RP in NHP
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    Results Available from GS030 Study for RP in NHP

    Recently, biopharmaceutical company GenSight Biologics ("GenSight") announced the publication of data from a study evaluating GS030-Drug Products (GS030-DP or "GS030") as a potential treatment option for retinitis pigmentosa (RP). Although…

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    First Patient Dosed in CA-4948 Trial for Hematologic Malignancies
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    First Patient Dosed in CA-4948 Trial for Hematologic Malignancies

    The first patient has been dosed in a Phase 1 clinical trial, which is exploring Curis Inc.'s CA-4948 in conjunction with ibrutinib for hematologic malignancies. Examples of hematologic malignancies include…

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    Polish Agency Awarded Grant for Annamycin Clinical Trial for STS
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    Polish Agency Awarded Grant for Annamycin Clinical Trial for STS

    In a recent press release, pharmaceutical company Moleculin Biotech, Inc. ("Moleculin") shared a recent advance in the sphere of medical and health research. Agencja Badań Medycznych, a Polish agency which contributes…

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    After Failed Parkinson’s Trial, Sanofi Pauses Drug Development Programs
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    After Failed Parkinson’s Trial, Sanofi Pauses Drug Development Programs

    During clinical trials, researchers work to advance clinical knowledge, build an understanding of certain diseases or conditions, and learn more about a new drug, surgical device, or behavioral modification technology. However,…

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    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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