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Johnson & Johnson's nipocalimab granted U.S. FDA Breakthrough Therapy Designation for the treatment of individuals at high risk for severe hemolytic disease of the fetus and newborn (HDFN)

/PRNewswire/ Johnson & Johnson today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation (BTD) for.

United statesPrnewswire johnsonBridget kimmelKatie abouzahrDrug administrationExchange commissionHematology am soc hematol educ programJanssen research developmentJanssen biotech incNone of the janssen pharmaceutical companiesNational library of medicineJanssen pharmaceutical companiesFetal medicine foundation world congressBreakthrough therapy designationVice presidentMaternal fetal immunology disease area leader

Landmark Phase 3 MARIPOSA Study Shows

Early data show an overall survival trend favoring the combination of amivantamab and lazertinib compared to osimertinib; consistent results seen in.

South koreaUnited statesSoult ukpyolsiRegion flamandeRepublic of koreaJannsen cilag gmbJanssen cilag gmbByoung chul choEuropean society for medical oncologyAmerican lung associationEuropean unionJanssen research developmentYuhan corporationJanssen biotech incYonsei university college of medicineNational cancer institute

First Results with Erdafitinib-Releasing Intravesical

Investigational TAR-210 first-in-human results highlight the potential for local sustained release of erdafitinib with a novel intravesical delivery.

Comunidad autonoma de catalunaRegion flamandeIndianj urolJanssen cilag gmbJanssen pharmaceuticaJeffrey infanteMartin vogelUrology care foundationJanssen research developmentNone of the janssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonEuropean society for medical oncologyAstex therapeuticsOncology early clinical developmentTranslational researchAstex announces new drug discovery alliance

Results from Phase 2 THOR-2 Study Showed Improved Rates of

Data from Cohort 1 of the Phase 2 THOR-2 study showed oral erdafitinib reduced the risk of disease recurrence or death compared with intravesical.

Region flamandeUnited kingdomJanssen cilag gmbIndianj urolKiran patelJames wf cattoMartin vogelJanssen pharmaceuticaAstex announces new drug discovery allianceUniversity of sheffieldClinical developmentJanssen researchNone of the janssen pharmaceutical companiesExchange commissionJanssen pharmaceutical companiesDrug administration

New Safety Data Suggests SPRAVATO®▼ (Esketamine Nasal

Beerse, Belgium, Oct. 08, 2023 (GLOBE NEWSWIRE) The new safety data is from the ESCAPE-TRD Phase 3b study1Additional findings from this study showed.

United kingdomComunidad autonoma de catalunaRegion flamandeClin psychopharmacolClin neurosciEduard vietaEuropean medicines agencyDrug administrationPatient health questionnaireExchange commissionNone of the janssen pharmaceutical companiesPsychology service of the hospital clEuropean college of neuropsychopharmacology congressJanssen cilag ltdWorld health organizationJanssen cilag international

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