Anna is from England and recently finished her undergraduate degree. She has an interest in medicine and enjoys writing. In her spare time she likes to cook, hike, and hang out with cats.

    A Supplemental New Drug Application Has Been Submitted for a Potential Treatment of Immune Thrombocytopenia
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    A Supplemental New Drug Application Has Been Submitted for a Potential Treatment of Immune Thrombocytopenia

    Dova Pharmaceutics has submitted a supplemental New Drug Application to the US FDA on behalf of Doptelet® (avatrombopag), which is being researched as an investigational treatment of immune thrombocytopenia in…

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    A Study of Huntington’s Disease in Mice Suggests an ‘Early Stage’ of the Condition

    A recent study using mice suggests that Huntington’s disease may begin to show symptoms early on in life. For more detailed information, you can read the source article here, at…

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    Eiger and the FDA Have Met to Disucss Lonafarnib, an Investigational Treatment For Progeria
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    Eiger and the FDA Have Met to Disucss Lonafarnib, an Investigational Treatment For Progeria

    The US Food and Drug Administration and Eiger BioPharmaceuticals, Inc. have met to discuss lonafarnib, a drug being investigated as a potential treatment for Hutchinson-Gilford Progeria Syndrome. For more detailed…

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    Researchers are Looking for People Diagnosed with Multiple Sclerosis to Take Part in a Phone App Study
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    Researchers are Looking for People Diagnosed with Multiple Sclerosis to Take Part in a Phone App Study

    Researchers are looking for participants to take part in a study investigating whether a mobile app could benefit patients with multiple sclerosis. For more information about this study and how…

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    Researchers Announce Positive Results From a Phase I Study of a Therapy For Acute GvHD
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    Researchers Announce Positive Results From a Phase I Study of a Therapy For Acute GvHD

    Cynata Therapeutics, an Australian stem cell and regenerative medicine company, has announced positive results from a Phase 1 clinical trial of CYP-001, the CymerusTM mesenchymal stem cell product candidate. The study…

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    The US FDA Has Approved Takhzyro for the Treatment of Hereditary Angioedema
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    The US FDA Has Approved Takhzyro for the Treatment of Hereditary Angioedema

    The US Food and Drug Administration has approved a drug called TakhzyroTM (lanadelumab-flyo) for the treatment of hereditary angioedema. This approval was based on supporting evidence from several studies, including from…

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    Two Clinical Studies of an Experimental Drug for Duchenne Muscular Dystrophy Have Been Stopped
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    Two Clinical Studies of an Experimental Drug for Duchenne Muscular Dystrophy Have Been Stopped

    According to a recent press release, Pfizer Inc. has terminated two on-going clinical trials that were investigating domagrozumab (PF-06252616) as a potential treatment for Duchenne muscular dystrophy. This decision follows…

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    A Study of an Investigational Acute Myeloid Leukaemia and Myelodysplastic Syndrome Drug Has Completed Enrolment

      The company Imago Biosciences, which focuses on developing anti-cancer therapies, is carrying out a Phase 1/2a clinical study of an investigational drug called IMG-7289 as a potential treatment for…

    Continue Reading A Study of an Investigational Acute Myeloid Leukaemia and Myelodysplastic Syndrome Drug Has Completed Enrolment

    Researchers at UNC Are Experimenting With a New Way to Deliver Drugs For Medulloblastoma

    A team of researchers from the University of North Carolina have been exploring an experimental method of delivering drugs to medulloblastoma that involves converting skin cells into stem cells that…

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    Orphan Drug Designation Has Been Granted to a Gene Therapy for Bietti’s Crystalline Dystrophy
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    Orphan Drug Designation Has Been Granted to a Gene Therapy for Bietti’s Crystalline Dystrophy

    Reflection Biotechnologies has announced that the US Food and Drug Administration has awarded Orphan Drug Designation to their RBIO-101 program, which is focused on a gene therapy designed to treat…

    Continue Reading Orphan Drug Designation Has Been Granted to a Gene Therapy for Bietti’s Crystalline Dystrophy
    Researches Are Developing a Way to Predict Who Will Respond to Checkpoint Inhibitors for Melanoma
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    Researches Are Developing a Way to Predict Who Will Respond to Checkpoint Inhibitors for Melanoma

    A recent study, carried out by researchers from the National Cancer Institute (part of the NIH) and several other universities, outlines a potential new method of predicting whether immune checkpoint…

    Continue Reading Researches Are Developing a Way to Predict Who Will Respond to Checkpoint Inhibitors for Melanoma

    Research Shows a Drug For Transthyretin Amyloid Cardiomyopathy May Significantly Reduce Mortality in Patients

      Pfizer has released the primary results from the Phase 3 clinical trial of tafamidis, an investigational drug being researched as a potential treatment for transthyretin amyloid cardiomyopathy. For more…

    Continue Reading Research Shows a Drug For Transthyretin Amyloid Cardiomyopathy May Significantly Reduce Mortality in Patients
    The First Patient Has Been Dosed on a Study of a Drug For Duchenne Muscular Dystrophy
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    The First Patient Has Been Dosed on a Study of a Drug For Duchenne Muscular Dystrophy

    The Australian biopharmaceutical company Antisense Therapeutics has announced that the first patient has been dosed on a Phase 2 clinical trial of the investigational drug ATL1102, which is being developed…

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    A Drug Being Developed to Treat Acute Myeloid Leukaemia Has Been Given a Generic Drug Name

    The United States Adopted Name Council, which selects simple, new, and informative generic drug names, has approved ‘Onvansertib’ as the generic name for PCM-075. PCM-075 is an investigational drug that…

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