New York: Drugmakers Pfizer, BioNTech and Moderna are expected to reap billions of dollars from Covid-19 booster shots in a market. This development could rival the $6 billion in annual sales for flu vaccines for years to come, analysts and healthcare investors have said. For several months, the companies have said they expect that fully inoculated people will need an extra dose of their vaccines to maintain protection over time and to fend off new coronavirus variants.
Now a growing list of governments, including Chile, Germany and Israel, have decided to offer booster doses to older citizens or people with weak immune systems in the face of the fast-spreading Delta variant.
The US Food and Drug Administration (FDA) authorised a booster dose of vaccines from Pfizer and Moderna for people with compromised immune systems.
Pfizer, along with its German partner BioNTech , and Moderna have together locked up over $60 billion in sales of the shots just in 2021 and 2022. The agreements include supply of the initial two doses of their vaccines as well as billions of dollars in potential boosters for wealthy nations.
Going forward, analysts have forecast revenue of over $6.6 billion for the Pfizer/BioNTech shot and $7.6 billion for Moderna in 2023, mostly from booster sales. They eventually see the annual market settling at around $5 billion or higher, with additional drugmakers competing for those sales.
The vaccine makers say that evidence of waning antibody levels in vaccinated people after six months, as well as an increasing rate of breakthrough infections in countries hit by the Delta variant, support the need for booster shots.
Some early data suggests that the Moderna vaccine, which delivers a higher dose at the outset, may be more durable than Pfizer’s shot, but more research is needed to determine whether that is influenced by the age or underlying health of the people vaccinated.
As a result, it is far from clear how many people will need boosters, and how often. The profit potential of booster shots may be limited by the number of competitors who enter the market. In addition, some scientists question whether there is enough evidence that boosters are needed, particularly for younger, healthy people. The World Health Organisation (WHO) has asked governments to hold off on booster shots until more people worldwide receive their initial doses.
“We don’t know what the market forces will be,” Moderna president Stephen Hoge was quoted as saying by ‘Reuters’ a week ago. “At some point, this will become a more traditional market – we will look at what are the populations at risk, what value are we creating, and what are the number of products that serve that value. That will ultimately impact price,” Hoge added.
A model in flu shots
If regular Covid-19 boosters are needed among the general population, the market would most resemble the flu shot business, which distributes more than 600 million doses per year. Four competitors split the US flu market, which is the most lucrative and accounts for around half the global revenue, according to Dave Ross, an executive at CSL’s flu vaccine unit ‘Seqirus’.
Flu vaccination rates in developed countries have settled at around 50 per cent of the population. Covid boosters would likely follow a similar pattern if approved widely, said Atlantic Equities analyst Steve Chesney.
Flu shots cost around $18 to $25 a dose, according to US government data and competition has kept price increases in check, with producers raising prices four or five per cent in 2021.
Pfizer and Moderna may have greater pricing power for their boosters, at least at the outset, until competitors arrive. Pfizer initially charged $19.50 per dose for its vaccine in the US and 19.50 euros for the European Union, but has already raised those prices by 24% and 25%, respectively, in subsequent supply deals.
AstraZeneca and Johnson & Johnson are both gathering additional data on boosters of their vaccines. Novavax, Curevac, and Sanofi could also potentially be used as boosters, though their vaccines have yet to receive any regulatory authorisation.
