CINCINNATI, July 13, 2021 (GLOBE NEWSWIRE) -- Meridian Bioscience, Inc. (NASDAQ: VIVO), a provider of diagnostic testing solutions and life science raw materials, today provided preliminary revenue results for its third quarter of fiscal 2021.
CINCINNATI, June 28, 2021 (GLOBE NEWSWIRE) -- Meridian Bioscience, Inc., a leading global provider of diagnostic testing solutions and life science raw materials, announced today that it has re-submitted its application for Emergency Use Authorization (EUA) to the U.S. Food and Drug Administration (FDA) for the company’s SARS-CoV-2 molecular diagnostic test on the Revogene® platform.
Caraway Therapeutics today announced an exclusive, collaboration and option agreement with AbbVie (NYSE: ABBV) to develop and commercialize Caraway’s small molecule therapeutics targeting TMEM175, a potassium ion channel critical to lysosomal function implicated in both Parkinson’s disease (PD) and other neurodegenerative disorders.
“The deal we got was as good as we had gotten if we had held onto the program for two, three, four years … The deal was nice enough to persuade us to do it now,” said Caraway CEO Martin Williams, adding that the biotech had talked to about 15 companies about potential partnerships.
IM HealthScience® (IMH®) today announced favorable results from the longest-running post-marketing surveillance study of its type. This study, called Functional Dyspepsia Safety Update at 24 months (FDSU24), is a real-world surveillance study reporting on the safety and tolerability profile of FDgard® (COLM-SST®). Using patented Site-Specific Targeting® (SST®) technology pioneered by IM HealthScience, FDgard is designed to rapidly deliver solid-state, individually triple-coated microspheres of caraway oil and l-Menthol to the duodenum, or upper belly, where they are needed most for the management of Functional Dyspepsia (FD, or recurring, meal-triggered indigestion).