Merck licenses innovative anti-cancer therapy LM-299 from LaNova Medicines

Merck licenses innovative anti-cancer therapy LM-299 from LaNova Medicines

In a strategic move to broaden its oncology portfolio, Merck & Co., Inc. (NYSE: MRK), recognized globally as MSD outside the U.S. and Canada, has announced an exclusive licensing agreement with LaNova Medicines Ltd., a Shanghai-based biotech company. This agreement grants Merck the global rights to develop, manufacture, and commercialize LM-299, an investigational bispecific antibody […]

Merck’s $1.3bn bet on cancer therapy: Inside the Modifi Biosciences acquisition

Merck’s $1.3bn bet on cancer therapy: Inside the Modifi Biosciences acquisition

Merck & Co., a global leader in pharmaceuticals, has acquired Modifi Biosciences, a cutting-edge biotech startup based in New Haven, Connecticut, for up to $1.3 billion. The agreement, which involves an upfront payment of $30 million, includes milestone-dependent payouts that could total over a billion dollars. This acquisition marks Merck’s latest move to expand its […]

Breakthrough liver cancer treatment: Merck’s new drug combo slashes disease progression risk by 34%

Breakthrough liver cancer treatment: Merck’s new drug combo slashes disease progression risk by 34%

Merck & Co., Inc. (known as MSD outside the United States and Canada) and Eisai Co., Ltd. have announced encouraging results from the first interim analysis of the Phase 3 LEAP-012 trial evaluating the efficacy of KEYTRUDA (pembrolizumab), an anti-PD-1 therapy by Merck, combined with LENVIMA (lenvatinib), an orally available multiple receptor tyrosine kinase inhibitor […]

Health Canada approves KEYTRUDA and Enfortumab Vedotin for advanced urothelial cancer

Health Canada approves KEYTRUDA and Enfortumab Vedotin for advanced urothelial cancer

Merck (NYSE: MRK), known as MSD outside the United States and Canada, has announced that Health Canada has granted approval for KEYTRUDA (pembrolizumab) in combination with enfortumab vedotin for the treatment of adult patients with unresectable locally advanced or metastatic urothelial cancer (mUC) who have not received prior systemic therapy for this condition. This decision […]

Merck secures exclusive global license for opevesostat from Orion Corporation

Merck secures exclusive global license for opevesostat from Orion Corporation

Merck (NYSE: MRK), also known as MSD outside the United States and Canada, has enhanced its strategic position in the oncology market by securing an exclusive global license for opevesostat (MK-5684/ODM-208) and other CYP11A1 targeting candidates, following a mutual agreement with Orion Corporation. This pivotal deal marks a significant advancement in the treatment of prostate […]

Merck to acquire EyeBio in $3bn deal to expand ophthalmology pipeline

Merck to acquire EyeBio in $3bn deal to expand ophthalmology pipeline

Merck (NYSE: MRK), also known as MSD outside of the United States and Canada, has announced a definitive agreement to acquire EyeBio Limited, a prominent ophthalmology-focused biotechnology company, in a deal worth up to $3 billion. This acquisition includes an upfront payment of $1.3 billion in cash, with additional developmental, regulatory, and commercial milestone payments […]

Merck announces over €300m investment in new bioprocessing center in South Korea

Merck announces over €300m investment in new bioprocessing center in South Korea

Merck has embarked on a monumental investment venture, injecting more than €300 million into the construction of a new Bioprocessing Production Center located in Daejeon, South Korea. This initiative stands as the most significant investment by Merck’s Life Science business sector in the Asia-Pacific region to date, underscoring the company’s dedication to expanding its operations […]

Merck’s KEYTRUDA shows 38% reduction in death risk for renal cell carcinoma patients in Phase 3 KEYNOTE-564 trial

Merck’s KEYTRUDA shows 38% reduction in death risk for renal cell carcinoma patients in Phase 3 KEYNOTE-564 trial

Merck & Co., Inc., a global healthcare leader, has recently unveiled groundbreaking results from its Phase 3 KEYNOTE-564 trial. This pivotal study demonstrates that KEYTRUDA, Merck’s innovative anti-PD-1 therapy, significantly reduces the risk of death by 38% compared to placebo, marking a milestone in adjuvant therapy for patients with renal cell carcinoma (RCC) post-nephrectomy. Presented […]

FDA approves Merck’s KEYTRUDA for advanced cervical cancer treatment

FDA approves Merck’s KEYTRUDA for advanced cervical cancer treatment

Merck, known as MSD outside of the United States and Canada, has received approval from the U.S. Food and Drug Administration (FDA) for KEYTRUDA, its anti-PD-1 therapy. This approval, in combination with chemoradiotherapy (CRT), is for the treatment of patients with International Federation of Gynecology and Obstetrics (FIGO) 2014 Stage III-IVA cervical cancer. The approval […]

Merck to acquire Harpoon Therapeutics for $680m to strengthen oncology pipeline

Merck to acquire Harpoon Therapeutics for $680m to strengthen oncology pipeline

Merck (NYSE: MRK), known as MSD outside the United States and Canada, and Harpoon Therapeutics, Inc. (Nasdaq: HARP) have entered a definitive agreement where Merck will acquire Harpoon for $23 per share in cash, totaling an approximate equity value of $680 million. This strategic acquisition aims to bolster Merck’s oncology pipeline with Harpoon’s advanced cancer […]

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