A France-based specialty vaccine company, Valneva SE, announced the initiation of a clinical study in sites across the United Kingdom for its inactivated, adjuvanted COVID-19 vaccine candidate, VLA2001, which consists of inactivated whole virus particles of SARS-CoV-2 with high S-protein density, in combination with two adjuvants, alum and CpG 1018.
VLA2001-201 is the first-in-human Phase 1/2 study that will evaluate three dose levels of VLA2001 (low, medium, high) for safety, tolerability, and immunogenicity in a two-dose schedule with intra muscular vaccinations three weeks apart.
Alok Sharma, UK Secretary of State for Business, Energy and Industrial Strategy, said in a press statement: "Thanks to significant investment from the UK government, we are doing all we can to ensure our country has the capabilities in place to produce hundreds of millions of doses of this vaccine for the UK, and those around the world.”