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CPhI and Pharma Intelligence announce 2022 editions of Pharma IPR India and Biopharma Conclave in Mumbai

Mumbai (Maharashtra) [India], September 14 (ANI/Newsvoir): Pharma Intelligence, now Citeline, one of the leading business intelligence providers and knowledge partners, is pleased to announce the 11th Pharma IPR India 2022, and the 4th edition of Biopharma Conclave 2022 organised by the Informa Markets division of Informa PLC. Biopharma Conclave 2022 will take place on September 15 and 16 at Aster, the St. Regis Mumbai, and Pharma IPR India 2022 is set convene from September 14th to 16th, 2022 a...
New Delhi Indian Biosimilars Poornachandra Tejasvi Biocon Biologics Slate Development Knowledge Partnership

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
Craig Tendler Christie Corbett Susan Stewart Janssen Research None Of The Janssen Pharmaceutical Companies Slate Development

Janssen: European Commission Approves IMBRUVICA (ibrutinib) in a Fixed-Duration Combination Regimen for Adult Patients with Previously Untreated Chronic Lymphocytic Leukaemia (CLL)

Approval marks the first all-oral, once-daily, fixed-duration Bruton's tyrosine kinase (BTK) inhibitor-based regimen for first-line treatment of CLL The Janssen Pharmaceutical Companies of Johnson
United States Noord Holland Craig Tendler Jenni Mildon Edmond Chan Arnon Kater

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European Commission Approves IMBRUVICA® (ibrutinib) in a Fixed-Duration Combination Regimen for Adul

Approval marks the first all-oral, once-daily, fixed-duration Brutonโ€™s tyrosine kinase (BTK) inhibitor-based regimen for first-line treatment of CLLBEERSE, Belgium--(BUSINESS WIRE)--The Janssen Pharmaceutical Companies of Johnson & Johnson announced today that the European Commission granted marketing authorisation...
United States Noord Holland Craig Tendler Jenni Mildon Edmond Chan Arnon Kater

Janssen Receives Positive CHMP Opinion for IMBRUVICA (ibrutinib) in a Fixed-Duration Combination Regimen for Adult Patients with Previously Untreated Chronic Lymphocytic Leukaemia (CLL)

The positive opinion is based on Phase 3 GLOW and Phase 2 CAPTIVATE study results, which investigated the efficacy and safety of ibrutinib plus venetoclax in patients with previously untreated CLL1
United States Craig Tendler Jenni Mildon Edmond Chan Hematology Am Soc Hematol Educ Program Janssen Biotech Inc

Phase 3 SHINE Results Show IMBRUVICA® (ibrutinib)-Based Combination Regimen Significantly Reduced the Risk of Disease Progression or Death in Older Patients with Newly Diagnosed Mantle Cell Lymphoma

/PRNewswire/ -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced primary results from the Phase 3 SHINE study (Abstract #7502), which...
United States Craig Tendler Michaell Wang Christie Corbett Global Medical Affairs Abbvie Company

Phase 3 SHINE Results Show IMBRUVICA® (ibrutinib)-Based Combination Regimen Significantly Reduced the Risk of Disease Progression or Death in Older Patients with Newly Diagnosed Mantle Cell Lymphoma

/PRNewswire/ -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced primary results from the Phase 3 SHINE study (Abstract #7502), which...
United States Craig Tendler Michaell Wang Christie Corbett Global Medical Affairs Abbvie Company

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