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J&J's next myeloma drug, Argenx's second act and a new question for Bluebird: 3 ASH takeaways

BioPharma ....

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Johnson & Johnson : New Results from the Phase 3 GLOW Study of Fixed-Duration Treatment with IMBRUVICA® (ibrutinib) Plus Venetoclax Demonstrate Robust Efficacy and Sustained Response in Older, Unfit Patients with Previously Untreated Chronic Lymphocytic Leukemia

NEW ORLEANS, December 10, 2022 - The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new four-year follow-up results from the Phase 3 GLOW study , which. | December 10, 2022 ....

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U.S. FDA Approves IMBRUVICA® (ibrutinib) as First and Only BTKi Treatment for Pediatric Patients with Chronic Graft-Versus-Host Disease

/PRNewswire/ The Janssen Pharmaceutical Companies of Johnson & Johnson announced today that the U.S. Food and Drug Administration (FDA) has approved. ....

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The Janssen Pharmaceutical Companies - U.S. FDA Approves IMBRUVICA (ibrutinib) as First and Only BTKi Treatment for Pediatric Patients with Chronic Graft-Versus-Host Disease

HORSHAM, PA - The Janssen Pharmaceutical Companies of Johnson & Johnson announced that the U.S. Food and Drug Administration has approved IMBRUVICA for the treatment of pediatric patients one. | August 25, 2022 ....

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IMBRUVICA's FDA approval gives hope for children with GvHD

IMBRUVICA, a treatment for chronic graft versus host disease in children aged one year and older, has been approved by the FDA. ....

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