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Adding Lynparza to Presurgical Chemo May Not Boost TNBC Outcomes

The addition of Lynparza to presurgical chemotherapy did not improve outcomes for patients with basal-like BRCA wild-type triple-negative breast cancer.

United kingdomSan franciscoUnited statesKaren pinilla albaDepartment of oncologyTrial consortiumUniversity of cambridge cancer researchUnited kingdom cancer centreUniversity of californiaHelen diller family comprehensive cancer centerAdding lynparzaCambridge cancer researchTriple negative breast cancer

Olaparib With Chemotherapy Does Not Elicit Improved Outcomes vs Chemotherapy Alone in BRCA Wild-Type TNBC

Olaparib on a gap schedule with chemotherapy does not improve responses vs chemotherapy alone in the neoadjuvant setting for patients with BRCA wild-type TNBC.

United kingdomUnited statesSan franciscoKaren pinilla albaOlaparib lynparzaUniversity of californiaDepartment of oncologyUnited kingdom cancer centreUniversity of cambridge cancer researchHelen diller family comprehensive cancer centerTrial consortiumPinilla albaCambridge cancer researchAdditional dataBreast cancerAacr annual meeting

Submission of Leqembi® (lecanemab-irmb) sBLA for IV maintenance dosing for the treatment of early Alzheimer s disease to the U S FDA completed

Stockholm, Sweden, April 1, 2024 - BioArctic AB s partner Eisai announced today that Eisai has submitted a supplemental Biologics License Application for monthly lecanemab-irmb intravenous .

United kingdomSaudi arabiaHong kongSouth koreaGreat britainLars lannfeltLecanemab leqembiOskar bossonNational institute onVp communicationsAlzheimer network trials unitNational institutes of healthClinical trial consortiumWashington university school of medicineEuropean unionDrug administration

Authors Reply: Cell Therapies in Diabetic Kidney Disease: I : Journal of the American Society of Nephrology

Authors Reply: Cell Therapies in Diabetic Kidney Disease: I : Journal of the American Society of Nephrology
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United statesTrial consortiumJournal of the american society nephrologyNovel stromal cell therapyDiabetic kidney diseaseAmerican society

BioArctic s partner Eisai submits supplemental Biologics License Application to FDA for traditional approval of LEQEMBI™ (lecanemab-irmb) for the treatment of Alzheimer s disease

Stockholm, January 7, 2023 - BioArctic AB s partner Eisai announced today they have submitted a supplemental Biologics License Application to the U.S. Food and Drug Administration supporting the. | January 7, 2023

Uppsala lanOskar bossonGunilla osswaldUppsala universityVp communicationsNational institutes of healthNational institute onDrug administrationWashington university school of medicineAlzheimer network trials unitClinical trial consortiumNational medical products administrationNasdaq stockholmBiologics license applicationAccelerated approvalAccelerated approval pathway