China NMPA Approves Promega MSI Detection Kit as Companion Diagnostic for KEYTRUDA® [Yahoo! Finance]
Merck & Company, Inc. (new) (MRK)
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Source: Yahoo! Finance
Instability (MSI) Detection Kit as a Class III in vitro diagnostic medical device in China. It is intended for use as a companion diagnostic to identify MSI-High (MSI-H) solid tumor patients for treatment with KEYTRUDA ® (pembrolizumab), Merck & Co., Inc., Rahway, NJ, USA's anti-PD-1 therapy. This is the first Promega companion diagnostic to receive NMPA approval. "This approval represents a step toward more personalized and effective cancer treatment in China," says Alok Sharma, Global Clinical Market Director at Promega. "We are proud to collaborate with pharmaceutical companies to deliver global solutions that expand access to innovative technologies and life-saving, effective therapies." China continues to face one of the world's highest cancer burdens, with solid tumors representing the vast majority of diagnoses nationwide. Despite advances in oncology care, most patients with advanced solid tumors ultimately progress after first-line therapy, creating a critical need for to
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Earnings
- 2/3/26 - Beat
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Sec Filings
- 2/3/26 - Form 8-K
- 1/28/26 - Form 4
- 1/28/26 - Form 4
- MRK's page on the SEC website