As the Johnson & Johnson vaccine moves closer to emergency use authorization, preliminary signs show its efficacy might not be as great as the previously-approved Pfizer and Moderna vaccines. Yet, it’s still efficient enough to be useful in the fight against the COVID-19 pandemic.
Operation Warp Speed chief adviser Moncef Slaoui expects “high efficacy” for the Johnson & Johnson vaccine, he said via Reuters, with an optimistic projection of 80-85% effectiveness. The single-dose vaccine doesn’t require the ultra-cold storage of the two vaccines currently in circulation in the U.S., giving it clear distribution advantages over the two-dose Pfizer and Moderna versions.
On Jan. 29, Johnson and Johnson said, via the Associated Press, that the vaccine was 66% effective against COVID-19 and 85% effective against the disease’s most serious symptoms.
“Gambling on one dose was certainly worthwhile,” Dr. Mathai Mammen, global research chief for J&J’s Janssen Pharmaceutical unit, told the AP.
A Jan. 13 Fortune article pointed out that the Johnson & Johnson vaccine “generated a long-lasting immune response in an early safety study, providing a glimpse at how it will perform in the real world as the company inches closer to approaching U.S. regulators for clearance.”
“More than 90% of participants made immune proteins, called neutralizing antibodies, within 29 days after receiving the shot,” the story noted, “and all participants formed the antibodies within 57 days. The immune response lasted for the full 71 days of the trial.”
That gave the company’s chief scientific officer, Paul Stoffels, optimism for the results of the latest phase of the clinical trials. “Looking at the antibodies, there should be good hope and good reason that the vaccine will work,” he said in an interview Jan. 12.
Should the timetable for those go as expected, the Johnson & Johnson vaccine, with its optimistic efficacy, should be approved for use as early as February, though the Fortune article foresaw a March approval.
CNN noted that results of Phase 1/2 trials, published Jan. 13 in the New England Journal of Medicine, “found either one or two doses of the vaccine generated both antibody and T-cell responses against the coronavirus.” The report also noted that the Ad26.COV2.S vaccine, which uses a weakened form of a common cold virus, is ruled safe for use, with side effects including headaches, body aches, and, in rare cases among the approximately 800 participants, fever.
For context, the Moderna and Pfizer vaccines are about 95% effective, while the Sputnik vaccine from Russia is 91.6% effective.
As CNBC noted, the U.S. Department of Health and Human Services announced this past August that it paid approximately $1 billion for 100 million doses of the vaccine August to Janssen—Johnson & Johnson’s pharmaceutical subsidiary—with an option to order an additional 200 million doses.
According to the AP, Johnson & Johnson “said its vaccine works consistently in a broad range of people: A third of participants were over age 60, and more than 40% had other illnesses putting them at risk of severe COVID-19, including obesity, diabetes, and HIV.”
In early February, Johnson & Johnson applied to the FDA for emergency use authorization. Assuming it’s approved, it’d be the third vaccine approved in the U.S. along with Pfizer and Moderna.
In South Africa, which recently paused its use of AstraZeneca because early trials showed it wasn’t effective against the variant that originated in that country, began using the Johnson & Johnson vaccine on its citizens. In late February, it was reported that the vaccine performed even better in South Africa than the original data showed.
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