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Novartis Scemblix®, with novel mechanism of action, approved by the European Commission for adult patients with chronic myeloid leukemia | Small Molecules

Novartis Scemblix®, with novel mechanism of action, approved by the European Commission for adult patients with chronic myeloid leukemia

United statesUnited kingdomEast hanoverNovartis scemblixHaseeb ahmadAndreas hochhausOncology at jena university hospitalAmerican society for clinical oncologyEuropean hematology associationEuropean commissionHead of the department hematologyApproval programEuropean unionEuropean medicines agencyNovartis pharmaceuticals corpCommittee for medicinal products human use

Novartis Pharma AG: Novartis receives positive CHMP opinion for Scemblix, a novel treatment for adult patients with chronic myeloid leukemia

With unique STAMP mechanism of action, Scemblix could provide a new option for patients in Europe with chronic myeloid leukemia (CML) who have suffered intolerance or inadequate response with at least

United statesEast hanoverIsabella zinckHaseeb ahmadAmy wolfNicole zinsli sommFloriana riccio furnariSamir shahParag mahantiJulie masowSloan simpsonAndreas hochhausAlina levchukOncology at jena university hospitalAmerican society for clinical oncologyEuropean hematology association

Accord Healthcare and Intas Pharmaceuticals Sued For Infringement Over Rydapt Cancer Drug

Plaintiffs Novartis Pharmaceuticals Corporation and Dana-Farber Cancer Institute, Inc. (Dana Farber) filed a complaint against defendants Accord

United statesNorth carolinaDana farberDana farber cancer institute incDrug administrationDelaware corporationAccord healthcare incPlaintiffs novartis pharmaceuticals corporationDunn crutcherIntas pharmaceuticalDana farber cancer instituteMiddle districtTyrosine kinase activity

Novartis Scemblix®, with novel mechanism of action, shows superior, long-term efficacy and consistent tolerability in 96-week follow-up of chronic myeloid leukemia trial

Scemblix® (asciminib) continues to show superior efficacy with more-than-two-fold improvement in major molecular response rate vs. Bosulif® (bosutinib) at 96.

United statesEast hanoverJeff legosJorgee cortesSloan simpsonPrnewswire novartisAmerican society of clinical oncologyEuropean hematology associationExchange commissionGlobal head of oncology hematology developmentApproval programAugusta universityNj novartis pharmaceuticals corporationGeorgia cancer centerNovartis pharmaceuticals corpClinical oncology

Investegate |NOVARTIS AG CHF0 50(REGD) Announcements | NOVARTIS AG CHF0 50(REGD): Novartis Scemblix®, with novel mechanism of action, shows superior, long-term efficacy and consistent tolerability in 96-week follow-up of chronic myeloid leukemia trial

Investegate announcements from NOVARTIS AG CHF0.50(REGD), Novartis Scemblix®, with novel mechanism of action, shows superior, long-term efficacy and consistent tolerability in 96-week follow-up of chronic myeloid leukemia trial

United statesEast hanoverNovartis scemblixIsabella zinckJeff legosAmy wolfNicole zinsli sommFloriana riccio furnariSamir shahParag mahantiJulie masowJorgee cortesSloan simpsonAlina levchukAmerican society of clinical oncologyEuropean hematology association

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