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Imago BioSciences (IMGO) Presents Positive Data from Ongoing Phase 2 Study of Bomedemstat in Advanced Myelofibrosis at ASH 2022

Imago BioSciences (IMGO) Presents Positive Data from Ongoing Phase 2 Study of Bomedemstat in Advanced Myelofibrosis at ASH 2022
streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.

United statesKristen pettitHugh young rienhoff jrEuropean hematology association annual meetingAmerican society of hematology annual meetingImago biosciences incErnestn morial convention centerUniversity of michiganWall streetAmerican societyHematology annual meetingTotal symptom scoreHugh young rienhoffChief executive officerPresentation titleAdvanced myelofibrosis

Imago BioSciences Presents Positive Data from Ongoing Phase 2 Study of Bomedemstat in Advanced Myelofibrosis at ASH 2022

Imago BioSciences Presents Positive Data from Ongoing Phase 2 Study of Bomedemstat in Advanced Myelofibrosis at ASH 2022
streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.

Redwood cityUnited statesKristen pettitZasadnyevoke canaleHugh young rienhoff jrEuropean hematology association annual meetingAmerican society of hematology annual meetingImago biosciences incErnestn morial convention centerUniversity of michiganEuropean medicines agencyLaurence wattsgilmartin groupAmerican societyHematology annual meetingTotal symptom scoreHugh young rienhoff

EMA validates GSK s application for myelofibrosis therapy

The European Medicines Agency (EMA) has validated GSK’s marketing authorization application (MAA) for momelotinib to treat myelofibrosis.

Drug administrationCommittee for medicinal products human useTransfusion independenceSplenic response rateTotal symptom scoreMedicinal productsHuman useNew drug applicationPrescription drug user fee act

EMA accepts momelotinib marketing application

The marketing authorisation application for momelotinib, a new oral treatment for myelofibrosis has been accepted by the EMA.

United statesAmerican society of hematologyAmerican society of clinical oncologyEuropean medicines agencyEuropean hematology associationDrug administrationCommittee for medicinal products human useTotal symptom scoreTransfusion independenceSplenic response rateMyelofibrosis symptom assessment formClinical oncologyAnnual meetingAmerican societyNew drug applicationMedicinal products

Karyopharm Therapeutics (KPTI) Q3 2022 Earnings Call Transcript

KPTI earnings call for the period ending September 30, 2022.

United statesMike masonAbi gray bairdAbi grayKevin strang jefferiesKevin strangMaury raycroftColleen kusyRichard paulsonReshma rangwalaBrian abrahamsDeric josephElhan webbSohanya chengFoundation medicineSelective inhibitor of nuclear