JnJ plans to seek USFDA authorization for booster shot of Covid-19 vaccine
New Delhi: Johnson & Johnson is planning to ask U.S. federal regulators this week to authorize a booster shot of its COVID-19 vaccine, the New York Times reported on Monday, citing officials familiar with the company's plans.
While scientists are divided over the need for booster shots when so many people in the United States and other countries remain unvaccinated, the Biden administration announced the push for an extra dose in August as part of an effort to shore up protection against the highly transmissible Delta variant.
The U.S. Food and Drug Administration (FDA) last week scheduled an Oct. 15 meeting of its expert advisory committee to discuss whether to grant emergency use authorization for a booster shot of J&J's vaccine.
Over 15 million Americans have received J&J's vaccine, which is administered as a single dose, according to the latest data from the Centers for Disease Control and Prevention.
The healthcare conglomerate last month said an additional second shot of its vaccine given about two months after the first increased its effectiveness to 94%, compared with 70% protection with the single dose.
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