Denmark-based vaccines company Bavarian Nordic A/S (CPH:BAVA) announced on Tuesday that the US Biomedical Advanced Research and Development Authority (BARDA) has exercised contract options totalling USD143.6m for the supply of its freeze-dried JYNNEOS smallpox/mpox vaccine.
Deliveries under the agreement are scheduled for 2026.
The contract includes conversion of previously manufactured bulk vaccine and supplemental payments for doses demonstrating extended shelf life. These payments will be invoiced pro rata with the delivery of the freeze-dried formulation.
JYNNEOS, approved by the US Food and Drug Administration in March 2025, offers improved shelf life and transportation and storage benefits over the liquid-frozen version.
Bavarian Nordic has worked with the US government on vaccine development and supply since 2003.
The company has now secured DKK2,650m in revenue for its Public Preparedness business in 2025, up DKK150m due to the exercised options. Its full-year guidance remains unchanged, with projected total revenues between DKK5,700m and DKK6,700m and an EBITDA margin of 26-30%.
(USD1=DKK6.59)
Ascentage Pharma receives China IND clearance for BTK degrader APG‑3288
FDA issues EUA for Boehringer Ingelheim's IVOMEC (ivermectin) 1% Injection
Cumberland Pharmaceuticals secures FDA Fast Track status for DMD heart‑disease therapy ifetroban
Hologic receives FDA approval for Aptima HPV assay as primary screening option
AbbVie submits FDA and EMA applications for new upadacitinib indication in NSV
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia