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Pfizer Inc and BioNTech SE say they have begun delivering doses of their experimental coronavirus vaccines for initial human testing in the United States.
Key points:
- There are no approved treatments or vaccines for COVID-19
- The US study is part of a global program underway in Germany
- Safety data on the vaccine may be available by late May
The US drug maker and German partner said on Monday if the vaccine proved to be safe and effective in trials, it could potentially be ready for wide US distribution by the end of the year, shaving several years off the typical vaccine development timeline.
The vaccine, which uses messenger RNA (mRNA) technology, has the potential to be among the first vaccines against the virus that has infected more than 1 million people in the United States and killed some 68,000.
There are currently no approved treatments or vaccines for the new coronavirus, though some drugs are being used on patients under an emergency use authorisation.
The US study is part of a broader, global program already underway in Germany, where BioNTech is based. Dosing there began last month.
Moderna is using similar technology for its vaccine being developed along with the US Government.
Phase I testing of that vaccine candidate has also begun, with mid-stage trials planned in the current quarter.
Pfizer said last week it hoped to receive emergency authorisation from the US Food and Drug Administration as early as October and could distribute up to 20 million doses by the end of 2020, with an eye toward producing hundreds of millions of doses next year.
Using synthetic mRNA technology could enable the vaccine to be developed and manufactured more quickly than traditional vaccines, the companies said.
Pfizer said last week it expected to make safety data on the vaccine available by late May.
Trial to involve 360 healthy volunteers
The trial will initially aim to test different dosing regimens of four potential vaccine candidates on around 360 healthy volunteers divided into a younger cohort and a group of seniors.
It will expand to more subjects after researchers determine which compounds and dosing regimens are most effective, said Kirsten Lyke, a director at the University of Maryland's Center for Vaccine Development and Global Health, which is participating in the trial.
Doses have already been administered to some volunteers at NYU Grossman School of Medicine and the University of Maryland School of Medicine.
Pfizer plans to expand the trial to sites across the United States in early July, and may ultimately enrol more than 8,000 participants, a company spokeswoman said.
If successful, the US clinical trial would be one of the fastest ever progressions of a vaccine from early stage studies to regulatory approval, compressing a development process that often takes as much as a decade to just over nine months.
BioNTech is producing the vaccine for the trials in its European manufacturing facilities.
Pfizer is investing in developing its own manufacturing capacity for the vaccine, and is preparing sites in Massachusetts, Michigan, Missouri and Belgium to begin producing it.
Both companies will jointly commercialise the vaccine, if approved.
Reuters
