First Wave soars on starting patient dosing in pancreatic disorder drug trial
** Shares of drug developer First Wave BioPharma Inc FWBI.O rise 21% to
$4.3 premarket
** Co begins patient dosing in mid-stage study of a treatment for a type of
pancreatic disorder associated with cystic fibrosis
** Topline results from the study expected by mid-2023 - FWBI
** Three clinical trial sites in the U.S. will be participating in the trial
designed to investigate the safety, tolerability and efficacy of the drug
** Cystic fibrosis is a genetic disorder that affects the cells that produce
mucus, sweat and digestive juices
** Stock down 98% in last 12 months
(Reporting by Aditya Samal)
((Aditya.Samal@thomsonreuters.com;))
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