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Merck & Co Inc's Keytruda Qlex (Pembrolizumab And Berahyaluronidase Alfa-pmph) has been approved in Japan for subcutaneous administration for all Keytruda (Pembrolizumab) indications approved in Japan.
MRK Merck's KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Approved in Japan for Subcutaneous Administration for All KEYTRUDA® (pembrolizumab) Indications Approved in Japan
Merck & Co.'s KEYTRUDA QLEX (pembrolizumab and berahyaluronidase alfa-pmph) injection for subcutaneous use has been approved by Japan's Ministry of Health, Labor and Welfare for all indications previously approved for KEYTRUDA. KEYJECT, the planned trademark for KEYTRUDA QLEX in Japan, can be administered in as little
Japan's health ministry has approved Merck & Co.'s subcutaneous Keytruda QLEX (KEYTRUDA) for all approved Keytruda indications in Japan. The product, to be marketed as Keyject, can be administered in 1 minute every 3 weeks or 2 minutes every 6 weeks.
Japan’s MHLW approved Merck’s KEYTRUDA QLEX (subcutaneous pembrolizumab combo) for all existing Keytruda indications in Japan, enabling 1–2 minute injections.
Merck said Japan’s MHLW approved KEYTRUDA QLEX (pembrolizumab and berahyaluronidase alfa-pmph) for subcutaneous administration for all KEYTRUDA indications approved in Japan.