KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Approved in Japan for SubQ Administration for All KEYTRUDA Indications Approved in Japan
“KEYJECT is the first and only subcutaneous immune checkpoint inhibitor available in Japan that can be administered by a healthcare provider in as little as one minute,” said Dr. Marjorie Green, senior vice president and head of oncology, global clinical development, Merck Research Laboratories. “This approval is a significant milestone for patients and healthcare providers in Japan and reflects our commitment to advancing new patient-centered care options like KEYJECT that offers patients two dosing options and more choices of health care settings where they can receive therapy.”
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