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BioWorld - Friday, July 24, 2026
Home » Merck & Co. Inc.

Articles Tagged with ''Merck & Co. Inc.''

Deal handshake and arrows sketch on chalkboard
Biopharma deals October 2025

Biopharma dealmaking climbs 17% in October to $31.9B

Nov. 14, 2025
By Amanda Lanier
No Comments
Biopharma dealmaking activity remained strong in October, with total deal value reaching $31.86 billion, a 17% increase from $27.15 billion in September and ranking as the second-highest month in 2025 after June’s $35.43 billion.
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Merck & Co. Inc. headquarters in Rahway, N.J.

Merck buys Cidara for $9.2B as Keytruda patent loss looms

Nov. 14, 2025
By Lee Landenberger
No Comments
Merck & Co. Inc. is buying Cidara Therapeutics Inc. for $9.2 billion to acquire a late-stage flu candidate and also to outrace blockbuster Keytruda’s looming patent expiration. CD-388, Cidara’s lead candidate, is in a phase III study of adolescents and adults for preventing influenza A and B in those who are at a high risk of developing complications.
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Pill with Euro currency symbol
FT Global Pharma and Biotech Summit

Trump’s MFN price deals a wake-up call for governments in Europe

Nov. 11, 2025
By Nuala Moran
No Comments
The industry has been complaining about the drug pricing and reimbursement policies of European governments for years, but only now with the Trump administration’s moves to enforce most favored nation (MFN) pricing and reduce the U.S./EU price gap are governments facing up to the reality that they will have to pay more for new drugs.
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Row of white dice with people icons, red die with scissors

Big pharma drives surge in biopharma job cuts in 2025

Nov. 4, 2025
By Amanda Lanier
No Comments
In 2025, the biopharma industry has undergone a wave of workforce reductions that surpasses previous years’ trends. Multiple major pharma companies have announced sizeable job cuts, driven by a convergence of shifting regulatory terrain, vaccine slowdowns and cost-structure rationalization.
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Keytruda Qlex

US FDA clears ‘one-minute’ Keytruda SC injection for solid tumors

Sep. 23, 2025
By Marian (YoonJee) Chu
No Comments
The U.S. FDA approved Merck & Co. Inc.’s Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph) injection on Sept. 19, making it the first and only subcutaneously (SC)-administered immune checkpoint inhibitor that can be administered in about a minute.
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Keytruda Qlex

US FDA clears ‘one-minute’ Keytruda SC injection for solid tumors

Sep. 22, 2025
By Marian (YoonJee) Chu
No Comments
The U.S. FDA approved Merck & Co. Inc.’s Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph) injection on Sept. 19, making it the first and only subcutaneously (SC)-administered immune checkpoint inhibitor that can be administered in about a minute.
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Halt of biopharma investment prompts emergency UK hearing

Sep. 16, 2025
By Nuala Moran
No Comments
The U.K.’s failure to join the dots from discovery research to patient access to innovative drugs was cited repeatedly by pharma leaders, who were called to an emergency hearing in parliament on Tuesday to explain decisions to pull out of promised capital investments.
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U.K. flag and capsules

Pharmas pull UK funding to protest drug rebates, market access

Sep. 15, 2025
By Nuala Moran
No Comments
Two months after it was launched, the wheels are coming off the U.K. government’s 10-year life sciences strategy, with pharma companies withholding promised capital investments in protest at the row over drug pricing. Merck & Co. Inc., Astrazeneca plc and Eli Lilly and Co. Inc. have said they are not going ahead with previously announced investments.
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Infection

Merck’s MK-8527 enables long-acting HIV-1 prevention

Sep. 15, 2025
No Comments
Nucleoside reverse transcriptase translocation inhibitors (NRTTIs) are a novel class of antiretroviral agents that inhibit HIV replication by targeting the viral reverse transcriptase enzyme and specifically blocking its translocation step during DNA synthesis, a critical process in the viral replication cycle.
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Medical Illustration showing lung cancer

WCLC 2025: Merck-Daiichi’s ADC posts a phase II win in lung cancer

Sep. 9, 2025
By Lee Landenberger
No Comments
Daiichi Sankyo Co. Ltd. and Merck & Co. Inc.’s antibody-drug conjugate (ADC) ifinatamab deruxtecan produced a confirmed 48.2% objective response rate in a phase II study of previously treated patients with extensive-stage small-cell lung cancer.
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