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Jan 24, 2024 United States Clinical and real-world evidence data support treatment with ERLEADA ® (apalutamide) and niraparib plus abiraterone acetate given with prednisone in patients with prostate cancer Additional updates will be presented on ...

Jun 21, 2024 Submission is supported by 48-week results from the Phase 3 GALAXI and GRAVITI programs TREMFYA® is the only IL-23 inhibitor to demonstrate strong endoscopic outcomes with subcutaneous (SC) induction, consistent with intravenous (IV) ...

Aug 23, 2024 Belgium First pan FGFR kinase inhibitor to be approved in the European Economic Area, for adults with unresectable or metastatic urothelial carcinoma and susceptible FGFR 3 alterations Approval based on THOR results, showing 36 percent ...

Dmitri Talantov, M.D. SENIOR MEDICAL DIRECTOR, JCI Dr. Talantov is a medical leader with Janssen Clinical Innovation based in California. He is responsible for development of novel clinical trial models, including direct-to-patient and hybrid trials and ...

MEGHA REDDY HEAD OF STRATEGY WORLD WITHOUT DISEASE ACCELERATOR As Head of Strategy for the World Without Disease Accelerator (WWDA), Megha leads the overall WWDA strategic planning, including the development of short- and long-term goals and objectives. ...

May 30, 2024 NEW BRUNSWICK, N.J., May 30, 2024 – Johnson & Johnson (NYSE: JNJ) today announced William N. (Bill) Hait, M.D., Ph.D., will retire from his position as Executive Vice President, Chief External Innovation and Medical Officer, in September ...

Getting into the Game: How pharmas are thinking about the microbiome for drug development Jan 06, 2017 Article Block Text:  BioCentury – May 9, 2016 Redirect URL:  http://www.biocentury.com/biotech-pharma-news/products/2016-05-09/how-pharmas-are-thinking ...

Patient Engagement Dec 12, 2019 Janssen partners directly with patients and caregivers as we develop medicines, improve clinical trials, and create educational materials and support programs. Article Block Text:  Janssen partners directly with patients ...

Mar 18, 2024 Czech Repubic Featured data include new results from the Phase 3 MARIPOSA study, which has received U.S. FDA Priority Review, and the Phase 1b PALOMA study of subcutaneous amivantamab  PRAGUE, CZECH REPUBLIC (March 18, 2024)-- Johnson & ...

Jun 03, 2024 Significantly lower infusion-related reactions seen with subcutaneous amivantamab compared with intravenous administration in new Phase 2 data CHICAGO (June 3, 2024) – Johnson & Johnson announced today new data from the Phase 2 PALOMA-2 ...

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