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AbbVie Receives Positive CHMP Opinion for Risankizumab (SKYRIZI®) for the Treatment of Adults with Moderately to Severely Active Ulcerative Colitis

AbbVie Receives Positive CHMP Opinion for Risankizumab (SKYRIZI®) for the Treatment of Adults with Moderately to Severely Active Ulcerative Colitis
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United statesKori wallaceVan asscheEdouard louisGastroenterol hepatolExchange commissionUniversity hospitalNational institute of diabetesBoehringer ingelheimAssociation between disease activityEuropean medicines agencyEuropean commissionCommittee for medicinal products human useDrug administrationEuropean unionCrohn colitis foundation of america

AbbVie Presents New Data Supporting Leading Gastroenterology Portfolio at 2024 Digestive Disease Week®

- AbbVie will present 15 abstracts, including three oral presentations, in Crohn s disease and ulcerative colitis reinforcing AbbVie s commitment to advancing.

United statesAnn gastroenterolGastroenterol hepatolAndrew anisfeldNational institute of diabetesInternational organization for the studyExchange commissionCrohn colitis foundationBoehringer ingelheimEuropean medicines agencyAmerican gastroenterological associationHealth economics cost of illnessSociety for surgery of the alimentary tractAbbvie incAmerican society for gastrointestinal endoscopyDrug administration

First-Line Treatment Options for AML

Catherine E. Lai, MD, MPH, discusses the current standard of care in the first-line treatment of patients with AML and which factors guide therapy selection.

Optimizing outcomesLong term managementPatients withLine treatment optionsAcute myeloid leukemiaAml overviewAcute myeloid leukemia first line treatmentsAml first line treatmentsAml first line treatment options7 3 regimenDaunorubicin and cytarabineInduction therapy

AMGEN HIGHLIGHTS HEMATOLOGY PORTFOLIO AT ASH 2023

AMGEN HIGHLIGHTS HEMATOLOGY PORTFOLIO AT ASH 2023
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Puerto ricoUnited arab emiratesCancer instituteAl qahirahUnited statesHong kongNew zealandSaudi arabiaMacau generalSan diegoJessica akopyanJustin claeysInotuzumab ozogamicinExchange commissionChemocentryx incTeneobio inc

FDA Approves Etrasimod for Moderately to Severely Active Ulcerative Colitis

The approval of oral, once-daily etrasimod 2 mg was based on positive data from the phase 3 ELEVATE UC 52 and ELEVATE UC 12 trials.

Michael chioreanEuropean medicines agencyCenter at swedish medicalDrug administrationSwedish medicalMarketing authorization applicationSeverely active ulcerative colitisVersus placeboInduction therapyEtrasimod velsipityUlcerative colitis