BERG Study Identifies a Genetic Factor Responsible For a Disproportionate Number of COVID-19 Cases Among African Americans

PRNewswire recently carried BERG’s announcement of the results of its COVID-19 clinical study. BERG, a biotech company based in Framingham, Mass., utilizes artificial intelligence in its research of diseases and…

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Oral Treatment for Inflammatory Bowel Disease Doses First Patients in Phase 1 Trial
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Oral Treatment for Inflammatory Bowel Disease Doses First Patients in Phase 1 Trial

As reported in BioSpace; trials for an oral treatment to treat inflammatory bowel disease (IBD) by Morphic Therapeutics has just dosed their first healthy subjects in the Phase 1 trial.…

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Study Identifies Predictive Tools to Shorten Active Surveillance Required in Prostate Cancer
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Study Identifies Predictive Tools to Shorten Active Surveillance Required in Prostate Cancer

PracticeUpdate recently published an article relating to a study with the primary goal of lightening the burden that many males experience regarding long-term prostate surveillance. Active surveillance has been preferred…

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Experimental Treatment for Fabry Disease to be Made Available Under Expanded Access
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Experimental Treatment for Fabry Disease to be Made Available Under Expanded Access

According to a story from PR Newswire, Chiesi Global Rare Diseases and the biopharmaceutical company Protalix BioTherapeutics, Inc. have recently announced that they have launched an Expanded Access Program (EAP)…

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Potential Osteogenesis Imperfecta Treatment Receives Rare Pediatric Disease Designation
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Potential Osteogenesis Imperfecta Treatment Receives Rare Pediatric Disease Designation

According to a story from BioSpace, the biopharmaceutical company Mereo BioPharma Group recently announced that its investigational therapy setrusumab has earned Rare Pediatric Disease designation from the US Food and…

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New Investigative Therapy for Myelofibrosis Patients with Severe Thrombocytopenia is Making Headway

CTI BioPharma has just announced that they are submitting a NDA for Pacritinib as a new option for myelofibrosis patients who are facing severe thrombocytopenia. The thrombocytopenia is a result…

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Simponi Aria (Golimumab) Approved for Juvenile Arthritis Types pJIA and jPsA
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Simponi Aria (Golimumab) Approved for Juvenile Arthritis Types pJIA and jPsA

Recently, the Janssen Pharmaceutical Companies of Johnson & Johnson ("Janssen") announced the FDA approval of Simponi Aria (golimumab). The therapy is designed to treat pediatric patients (ages 2 or older)…

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The aHUS Foundation has Created a Medical Tracker for atypical Hemolytic Uremic Syndrome Patients

aHUS Tracking Atypical hemolytic uremic syndrome (aHUS) is a rare disease that causes blood clots to form within the small blood vessels in the kidneys. These clots lead to organ damage…

Continue Reading The aHUS Foundation has Created a Medical Tracker for atypical Hemolytic Uremic Syndrome Patients