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[While the treatment landscape has evolved, an unmet need remains for appropriate patients newly diagnosed with certain types of advanced urothelial carcinoma who are not eligible for platinum-containing chemotherapy," said Dr. Scot Ebbinghaus, vice president, clinical research, Merck Research Laboratories. [We are confident in the role KEYTRUDA will continue to play for these patients who have few other treatment options and are working with urgency to advance studies to help more patients living with bladder and other types of cancer."
In addition to this first-line indication, KEYTRUDA is approved for the treatment of patients with locally advanced or mUC who have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. KEYTRUDA is also approved for the treatment of patients with Bacillus Calmette-Guerin-unresponsive, high-risk, non-muscle invasive bladder cancer with carcinoma in situ with or without papillary tumors who are ineligible for or have elected not to undergo cystectomy.
Merck has an extensive clinical development program in bladder cancer and is advancing multiple studies evaluating KEYTRUDA as monotherapy and in combination with other anti-cancer therapies across multiple lines of therapy.
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Privacy statement: Your privacy is very important to Us. Our company promises not to disclose your personal information to any external company with out your explicit permission.