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Updated Data from the BRUIN Phase 1/2 Study of Pirtobrutinib in Chronic Lymphocytic Leukemia and Mantle Cell Lymphoma Presented at the 2023 ASH Annual Meeting

/PRNewswire/ Eli Lilly and Company (NYSE: LLY) today announced updated clinical data from the international Phase 1/2 BRUIN trial of pirtobrutinib, a.

United statesEli lillyPrnewswire eli lillyKyle owensDavid hymanJoe fletcherMatthews davidsDana farber cancer instituteAmerican society of hematologyLilly united statesLaboratory abnormalitiesExchange commissionAmerican societyAnnual meetingDana farber cancerCommon terminology criteria

New Analyses Demonstrate Versatility and Continued Efficacy of TALVEY™ in the Treatment of Patients with Relapsed or Refractory Multiple Myeloma

/PRNewswire/ Johnson & Johnson announced today an analysis from the Phase 1/2 MonumenTAL-1 study of TALVEY™ (talquetamab-tgvs) in patients with relapsed or.

United statesSan franciscoChristie corbettSatu glaweChristoph heuckAmerican society of hematologyNone of janssen research developmentHematology clinical developmentEuropean commissionJanssen research developmentEastern cooperative oncology groupJanssen biotech incUniversity of californiaMyeloma programInternational myeloma working groupExchange commission

Menarini Group Presents New Progression-Free Survival Data from EMERALD Clinical Study of ORSERDU(R) (Elacestrant) in Clinically Relevant Subgroups of Patients with ER+, HER2- Metastatic Breast Cancer (mBC) with ESR1 Mutations at SABCS 2023

This new post hoc analysis of the Phase 3 EMERALD trial evaluatedelacestrant in the endocrine-sensitive population (CDK4/6 inhibitor duration of at least 12 months) with tumors harboring ESR1 mutations.This analysisshows a clinically meaningful

United statesElcin barker ergunMenarini stemlineMenarini groupElacestrant clinical development programUt health san antonioMenarini group stemline therapeuticMd anderson cancer centerStemline therapeutics incStemline therapeuticsAntonio breast cancer symposiumVirginia kaklamaniSan antonioSafety informationStemline therapeuticFetal toxicity

Karyopharm Shares Data at ASH 2023 Showing Strong SVR and TSS Durability Observed from Phase 1 Study of Selinexor 60mg and Ruxolitinib in JAK Inhibitor (JAKi)-Naïve Myelofibrosis Patients, with no SVR or TSS Progressions Observed As of the Data Cutoff(1)

Biomarker Data from Phase 1 Study of Selinexor in Combination with Ruxolitinib in Treatment-Naïve Myelofibrosis (MF) Suggestive of Disease Modification

United statesUnited kingdomHong kongSouth koreaKyongsang buktoKapila vigesReshma rangwalaKaryopharm selective inhibitor of nuclear exportDrug administrationExchange commissionInformation departmentPrnewswire karyopharm therapeutics incSelective inhibitor of nuclear exportAmerican society of hematology annual meetingKaryopharm therapeutics incUniversity of utah

VEGZELMA® (bevacizumab-adcd) receives preferred formulary status with Ventegra® for commercially insured patients

VEGZELMA® (bevacizumab-adcd) receives preferred formulary status with Ventegra® for commercially insured patients
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United statesNew jerseyTom nusbickelRobertt taketomoLindsey lucentaPharmacy services administrationVentegra specialty inclusion programPharmacy services administratorBenefits managerFormulary shieldChief commercial offerCelltrion unitedMedical benefits managerCelltrion united statesImportant safetyWound healing complications