It would be “unacceptable” for French drug giant Sanofi to give priority to the US market if it develops a Covid-19 vaccine, a French minister has warned.
Deputy Finance Minister Agnès Pannier-Runacher was responding to comments by Sanofi CEO Paul Hudson, who said “the US government has the right to the largest pre-order because it’s invested in taking the risk”.
Many labs worldwide are involved in research to find a Covid-19 vaccine.
Vaccines usually take years to develop.
“For us, it would be unacceptable for there to be privileged access to such and such a country for financial reasons,” Ms Pannier-Runacher told France’s Sud Radio.
Earlier this month the EU chaired a global online summit to boost coronavirus research, and secured pledges of $8bn (£6.5bn) from some 40 countries and donors. The funding is aimed at developing a coronavirus vaccine and treatments for Covid-19.
The UK co-hosted the summit but the US and Russia did not take part.
On Thursday Sanofi’s chief in France, Olivier Bogillot, said “the goal is to have this vaccine available to the US as well as France and Europe at the same time”.
Speaking on French news channel BFMTV, he said that would only be possible “if Europeans work as quickly as the Americans”, and added that the US government had pledged to spend “several hundreds of millions of euros”.
Sanofi’s Covid-19 vaccine research is partly funded by the US Biomedical Advanced Research and Development Authority (Barda).
But Sanofi has received tens of millions of euros in tax credits from the French government in recent years to help its research.
Last month Sanofi also teamed up with Britain’s GlaxoSmithKline (GSK) to work on a vaccine, though trials have not yet started.
Sanofi’s head of vaccine research, John Shiver, says “we are using an existing technology that was designed for influenza, and we’re applying it to the new virus that causes Covid-19 disease”.
Sanofi says GSK “will contribute its adjuvant technology, an ingredient added to enhance the immune response, reduce the amount of vaccine protein required per dose and improve the chances of delivering an effective vaccine that can be manufactured at scale”.
The candidate vaccine is expected to enter clinical trials in the second half of 2020 and to be available by the second half of 2021.