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ENYO Pharma Announces Positive Vonafexor (EYP001) Results for the LIVIFY Phase 2a Study in F2-F3 NASH Patients over 12 weeks

ENYO Pharma Announces Positive Vonafexor (EYP001) Results for the LIVIFY Phase 2a Study in F2-F3 NASH Patients over 12 weeks
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Axcella Announces Initiation of EMMPACT℠ Phase 2b Clinical Trial of AXA1125

Axcella Announces Initiation of EMMPACT℠ Phase 2b Clinical Trial of AXA1125 Initial clinical sites activated and patient screening underway Potential for AXA1125 to serve as a first-line therapy for patients with nonalcoholic steatohepatitis (NASH) CAMBRIDGE, Mass. (BUSINESS WIRE) Axcella (Nasdaq: AXLA), a clinical-stage biotechnology company pioneering a new approach to treat complex diseases and improve health using endogenous metabolic modulator (EMM) compositions, today announced that it has activated initial clinical sites and begun patient screening for its EMMPACT Phase 2b clinical trial of AXA1125, the company’s multi-targeted oral product candidate for the treatment of NASH. “NASH is the quintessential complex disease, involving the dysregulation of numerous biological pathways and impacting an enormous, heterogenous global population,” said Stephen A. Harrison, M.D., Medical Director of Pinnacle Clinical Research in San Antonio, TX, visi

ChronWell, Inc Adds Stephen Harrison, MD to Advisory Board

Share this article FORT LAUDERDALE, Fla., Feb. 17, 2021 /PRNewswire/  ChronWell, Inc., a digital health and technology-enabled remote care management company, today announced that Stephen Harrison, MD, FACP, FAASLD, has been added to the company s Board of Advisors. I am excited about the prospect of working with the ChronWell team to further it s important work in using data and digital tools to help patients and practices together achieve better outcomes, said Dr. Harrison. With ChronWell s deep experience in harnessing clinical data, and scientific approach, I m anticipating great strides in digital healthcare in a variety of specialties, beginning with gastroenterology and liver disease.

Can-Fite Reports on Progress With Its Namodenoson NASH Program

Can-Fite Reports on Progress With Its Namodenoson NASH Program Can-Fite Reports on Progress With Its Namodenoson NASH Program Can-Fite BioPharma Ltd. (NYSE American: CANF) (TASE:CFBI), a biotechnology company advancing a pipeline of proprietary small molecule drugs that address inflammatory, cancer and liver diseases, today announced the following progress with its Namodenoson drug candidate for non-alcoholic steatohepatitis (NASH) treatment: The Company is currently engaged in the design of a Phase IIb study for Namodenoson in the treatment of NASH. The protocol is being developed in conjunction with leading Key Opinion Leaders (KOLs) in NASH and liver diseases including Dr. Scott Friedman, Chief of the Division of Liver Diseases at the Icahn School of Medicine at Mount Sinai in New York, and Dr. Stephen A. Harrison, Medical Director of Pinnacle Clinical Research, both of whom were involved in the design of Namodenosons successfully completed Phase II study in NAFLD/NASH which

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