** Shares of drug developer Magenta Therapeutics Inc
MGTA.O fall ~42% to $0.48
** Co stops dosing patients at the cohort 4 dosing level in
drug MGTA-117's early-to-mid-stage trial after dose-limiting
toxicities (DLTs) were observed in the second and third dosed
participants
** The toxicity in patients involved a respiratory serious
adverse event (SAE)
** The drug is being studied to treat acute myeloid leukemia
(AML) and myelodysplastic syndrome (MDS)
** Both AML and MDS are groups of cancers associated with
the blood and bone marrow
** Co says it reported the clinical data of first observed
DLT to the U.S. FDA; adds information applicable to the DLT
event in the second participant is forthcoming
** Magenta now plans to continue enrollment and dose
additional participants at the Cohort 3 dose level
** Including session's fall, stock down 88.6% YTD
(Reporting by Pratik Jain in Bengaluru)
((Pratik.Jain@thomsonreuters.com;))