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US pharma giant Merck & Co is to buy CN201, an investigational clinical-stage bispecific antibody for the treatment of B-cell associated diseases, from privately-held Chinese biotech Curon Biopharmaceutical.
Merck has struck a deal worth up to $1.3 billion to buy an investigational drug targeting B-cell associated diseases.
On CNBC''s “Mad Money Lightning Round,” Jim Cramer recommended buying Merck & Co., Inc . (NYSE: MRK ). “I have tremendous, tremendous faith in what Robert Davis [CEO of Merck] is doing,” he added. When asked about Teladoc Health, Inc (NYSE: TDOC ), he said, “What''s going on there, right now we''ve got this Cathie Wood , she sells the stock almost every day. She bought it much higher, it''s really painful to watch.” Fortinet, Inc . (NASDAQ: FTNT ) reported a “very good” quarter, he said. “I remain committed to Nikesh Arora [CEO of Palo Alto … Full story available on Benzinga.com
Abnormal B cells can cause a range of diseases, from autoimmune diseases to cancers.
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KENILWORTH (NJ) (dpa-AFX) - Merck & Co Inc. (MRK) on Friday said it has agreed to acquire CN201, an investigational bispecific antibody for the treatment of B-cell associated diseases from Curon B…
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and Curon Biopharmaceutical (Curon), a privately held biotechnology company, today announced that the companies have entered into a definitive agreement under which Merck, through a subsidiary, has agreed to acquire CN201, a novel investigational clinical-stage bispecific antibody for the treatment of B-cell associated diseases. Jetzt den vollständigen Artikel lesen
Merck to acquire novel bispecific antibody CN201 for $700M upfront, expanding its oncology pipeline. Deal includes $600M in potential milestones. Learn about the promising treatment for lymphoma and leukemia.
On Thursday, Merck & Co Inc (NYSE: MRK ) announced discontinuing the Phase 3 KeyVibe-008 trial based on an independent Data Monitoring Committee (DMC) recommendation . The trial is evaluating the investigational fixed-dose combination (coformulation) of vibostolimab and Keytruda (pembrolizumab), in combination with chemotherapy, compared to Roche Holdings AG’s (OTC: RHHBY ) Tecentriq (atezolizumab) in combination with chemotherapy, for the first-line treatment of patients with extensive-stage small cell lung cancer (ES-SCLC). Also Read: FDA Declines To Approve Merck-Daiichi Sankyo Partnered Lung Cancer Drug . At a pre-planned analysis, data showed that the primary endpoint of overall … Full story available on Benzinga.com
Merck is winding down a late-stage test of its anti-TIGIT candidate vibostolimab in small-cell lung cancer after it showed early signs of poor efficacy, in another blow to the TIGIT space. The Phase 3 KeyVibe-008 trial was investigating a fixed-dose combination of vibostolimab with Keytruda plus standard-of-care chemotherapy. These therapies