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BURLINGTON, N.C. — LabCorp (NYSE: LH), a global leader of innovative and comprehensive laboratory services, today announced the U.S. Food and Drug Administration (FDA) has approved its nAbCyte™ Anti-AAVRh74var HB-FE Assay, a companion diagnostic (CDx) to determine patient eligibility for treatment with BEQVEZ™ (fidanacogene elaparvovec-dzkt), Pfizer’s recently FDA-approved hemophilia B gene therapy. The...
SAN FRANCISCO, Calif. — Laguna Biotherapeutics, Inc. (Laguna), a clinical-stage biotechnology company focused on novel live bacterial therapeutics, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application, granting a “safe to proceed” for its lead clinical candidate from the QUAIL platform,...
Reporthive.com introduced key new research reports encompassing the Lambert-Eaton Myasthenic Syndrome (LEMS) Therapeutics market. The aim of the study is to provide market leaders with a revolutionary decision-making tool that covers key fundamentals of the Lambert-Eaton Myasthenic Syndrome (LEMS) Therapeutics market. The Report Covers Market Size, Share, product Segmentation, CAGR,...
HAIFA, Israel — MAGENTIQ EYE LTD., an Israeli based technology company founded in 2014, announced today that a comprehensive study on the performance of MAGENTIQ-COLO™ CADe version has been published in the prestigious Lancet Digital Health medical journal. The study, titled “A novel computer-aided polyp detection system in screening and...
TORONTO, Canada — The World Ovarian Cancer Coalition announced that a groundbreaking international study, “Experiences of Women with Ovarian Cancer in 22 Low- and Middle- Income Countries (Every Woman Study™ LMIC): a Cross-sectional Study,” published today in The Lancet Obstetrics, Gynaecology, & Women’s Health, is the very first comprehensive study capturing...