Denmark-based vaccines company Bavarian Nordic A/S (CPH:BAVA) announced on Tuesday that it has been awarded a government contract valued at more than DKK700m to supply its MVA-BN smallpox/mpox vaccine to an undisclosed country during 2026 and 2027.
Deliveries are scheduled to begin in 2026, with the majority of revenue expected to be recognised in 2027.
The company said it has now secured approximately DKK2.2bn in Public Preparedness contracts for 2026, an increase of about DKK200m compared to the level previously announced.
Bavarian Nordic maintained its full-year 2026 guidance, forecasting Public Preparedness revenue of DKK2.3–2.5bn and total revenue of DKK5.5–5.7bn, with an EBITDA margin of approximately 28%.
The MVA-BN vaccine is the only non-replicating mpox vaccine approved in multiple markets, including the USA, EU/EEA, UK, Canada, Switzerland, Singapore, and Mexico.
The product was originally developed in collaboration with the US government as a smallpox vaccine suitable for immunocompromised individuals and is indicated for people at risk of smallpox or mpox infection.
FDA grants priority review for Genentech's Tecentriq in stage III dMMR/MSI-H colon cancer
Harbour BioMed IND for HBM7004 accepted by China's NMPA
Organon secures FDA approval expanding TOFIDENCE indications for CRS and paediatric COVID-19
Sanofi halts phase 3 MOBILIZE study of riliprubart in CIDP
Lynk Pharmaceuticals' partner Formation Bio doses first participant in BLKR201 Phase 1 trial
Verge Labs and Tenacia Biotechnology collaborate on advancing Tenacia's CNS pipeline
FDA grants rare paediatric disease designation to RedHill's opaganib
Bavarian Nordic secures DKK700m government vaccine contract
GSK to acquire Nuvalent for USD10.6bn to expand lung cancer portfolio
Argo Biopharma to present updated BW-20805 Phase II results at EAACI 2026 Congress
Curasight reports encouraging preliminary Phase 1 data for uTREAT in glioblastoma
Sciwind Biosciences reports positive study data on ecnoglutide versus semaglutide
Antengene presents first ATG-207 preclinical data at EULAR 2026
OriCell's GPC3 CAR-T Phase II hepatocellular carcinoma trial receives Chinese regulatory clearance