vimarsana.com
Home
Live Updates
Taiho Oncology, Inc.: FDA Approves Taiho's LYTGOBI (futibati
Taiho Oncology, Inc.: FDA Approves Taiho's LYTGOBI (futibati
Taiho Oncology, Inc.: FDA Approves Taiho's LYTGOBI (futibatinib) Tablets for Previously Treated, Unresectable, Locally Advanced or Metastatic Intrahepatic Cholangiocarcinoma
LYTGOBI (pronounced "light-GOH-bee") delivered an objective response rate of 42% and median duration of response of 9.7 months in the primary analysis of the pivotal clinical trial. LYTGOBI
Related Keywords
Oakville ,
Ontario ,
Canada ,
United States ,
New Jersey ,
Switzerland ,
Horsham ,
Saskatchewan ,
Massachusetts ,
Canadian ,
American ,
Kostenloser Wertpapierhandel ,
Teruhiro Utsugi ,
Lipika Goyal ,
Judy Kay Moore ,
Gastroenterol Hepatol ,
Tim Whitten ,
Taiho Pharmaceutical Co Ltd ,
Hospital Cancer Center ,
Drug Administration ,
Janssen Pharmaceutical Companies ,
Taiho Oncology Inc ,
Prnewswire Taiho Oncology Inc ,
Otsuka Holdings Co Ltd ,
Incyte Corporation ,
American Cancer Society ,
Taiho Oncology ,
Massachusetts General Hospital Cancer Center ,
Taiho Pharmaceutical ,
Senior Managing Director ,
Pigment Epithelial Detachment ,
Corneal Keratitis ,
Soft Tissue Mineralization ,
Prescribing Information ,
Oncology Media Contact ,
Rev Gastroenterol ,
Taiho ,
Ncology ,
Pproves ,
Ytgobi ,
Futibatinib ,
Tablets ,
Reviously ,
Reated ,
Unresectable ,
Ocally ,
Dvanced ,
Metastatic ,
Intrahepatic ,
Cholangiocarcinoma ,