May 2026 Roche and the Medicines Patent Pool signed a licensing agreement covering Xofluza, enabling selected generic manufacturers to develop and supply the influenza antiviral across 129 low- and middle-income countries while expanding global production preparedness.
January 2026 Merck completed its acquisition of Cidara Therapeutics, adding CD388, a long-acting investigational influenza antiviral, to its infectious-disease development portfolio.
November 2025 Merck agreed to acquire Cidara Therapeutics for approximately USD 9.2 billion, gaining control of CD388, an investigational therapy designed to provide extended protection against influenza A and B.
October 2025 Cidara Therapeutics advanced CD388 into Phase III clinical development for the prevention of symptomatic influenza among older adults and individuals with elevated risks of serious complications.
August 2025 Cidara Therapeutics expanded the planned Phase III development population for CD388 following discussions with the U.S. Food and Drug Administration, covering adults aged 65 years and older and younger high-risk patients.