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Syndax Presents Positive Pediatric Data from Pivotal AUGMENT-101 Trial of Revumenib in Relapsed, Refractory KMT2Ar Acute Leukemia at ASPHO Plenary Session

WALTHAM - Syndax Pharmaceuticals , a clinical stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announced the presentation of positive data from the pivotal.

United statesNeil gallagherSharon klahreSyndax pharmaceuticalsTime oncology review programExchange commissionAmerican society of hematology annual meetingAmerican society of pediatric hematology oncologyEuropean commissionHead of researchPlenary sessionPivotal phaseAcute leukemiaPediatric experienceHematology annualOrphan drug designation

Syndax Presents Positive Pediatric Data from Pivotal AUGMENT-101 Trial of Revumenib in Relapsed/Refractory KMT2Ar Acute Leukemia at ASPHO Plenary Session

– Consistent safety and efficacy profiles across adult and pediatric populations –

United statesSharon klahreNeil gallagherAmerican society of hematology annual meetingSyndax pharmaceuticalsHead of researchExchange commissionEuropean commissionTime oncology review programPrnewswire syndax pharmaceuticalsAmerican society of pediatric hematology oncologySyndax pharmaceuticals incPlenary sessionAcute leukemiaMeeting presentationsAmerican society

Syndax Announces FDA Priority Review Of NDA For Revumenib For Treatment Of R/R KMT2Ar Acute Leukemia

Syndax Announces FDA Priority Review Of NDA For Revumenib For Treatment Of R/R KMT2Ar Acute Leukemia
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Drug administrationMore such health newsSyndax pharmaceuticalsTime oncology review programPriority reviewNew drug applicationPrescription drug user fee act

Syndax Pharmaceuticals (SNDX) Granted FDA Priority Review of NDA for Revumenib

Syndax Pharmaceuticals (SNDX) Granted FDA Priority Review of NDA for Revumenib
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Michaela metzgerDrug administrationSyndax pharmaceuticals nasdaqTime oncology review programSyndax pharmaceuticalsPriority reviewNew drug applicationPrescription drug user fee actChief executive

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