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KEYTRUDA (pembrolizumab) Plus LENVIMA (lenvatinib) Approved in Japan for Radically Unresectable or Metastatic Renal Cell Carcinoma

25.02.2022 - Merck (NYSE: MRK), known as MSD outside the United States and Canada, and Eisai today announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) has approved the combination of KEYTRUDA, Merck’s anti-PD-1 therapy, plus LENVIMA, the ...
United States New Zealand Eisai Inc Eisai Europe Ltd Statement Of Merck Co Inc Exchange Commission

Results of Novel Clinical Study Show Adults with Moderately to Severely Active Ulcerative Colitis Achieved Higher Rates of Clinical Response, Clinical Remission, and Endoscopic Improvement at 12 Weeks with Guselkumab and Golimumab Combination Therapy Versus Either Monotherapy Alone

SPRING HOUSE, Pa., Feb. 19, 2022 /PRNewswire/ -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced data from a Phase 2a clinical trial that showed the combination of
United States Spring House British Columbia Brucee Sands Jan Wehkamp Bridget Kimmel
Source: wtva.com

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The Majority of Adults with Moderately to Severely Active Crohn's Disease in a Phase 2 Study Achieved Clinical Remission and Corticosteroid-Free Remission Through 48 Weeks with TREMFYA® (guselkumab)

/PRNewswire/ -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new results from the Phase 2 GALAXI 1 clinical trial showing the...
Spring House British Columbia United States Jan Wehkamp Bridget Kimmel None Of The Janssen Pharmaceutical Companies

The Majority of Adults with Moderately to Severely Active Crohn's Disease in a Phase 2 Study Achieved Clinical Remission and Corticosteroid-Free Remission Through 48 Weeks with TREMFYA® (guselkumab)

/PRNewswire/ -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new results from the Phase 2 GALAXI 1 clinical trial showing the...
Spring House British Columbia United States Jan Wehkamp Bridget Kimmel None Of The Janssen Pharmaceutical Companies

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