Johnson & Johnson one-shot Covid vaccine gets nod from FDA advisory panel

Vaccine, along with those from Pfizer and Moderna, should provide US with more than enough supply to vaccinate every person

The battle against Covid-19 took a major step forward on Friday as the US moved closer to distributing its first one-shot Covid-19 vaccine, after an independent expert advisory panel recommended drug regulators authorize the Johnson & Johnson vaccine for emergency use.

The authorization would be a significant boost to the Biden administration's vaccination plans, making Johnson & Johnson's vaccine the third available to the public. Janssen, Johnson & Johnson's vaccine subsidiary, told a congressional hearing this week that it expects to deliver 20m doses by March and a total of 100m doses before the end of June.