Moderna’s COVID-19 Vaccine 90% Effective Six Months After Final Dose

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US biotech company Moderna announced that its COVID-19 vaccine is 90 percent effective against all forms of the disease and 95 percent effective against severe disease.

In updated data from its phase III clinical trial published on Tuesday, the company also said its jab is more than 95 percent effective against severe disease 24 weeks after receiving the final dose.

The new data brings Moderna closer to filing for full approval with the U.S. Food and Drug Administration.

Moderna’s COVID-19 Vaccine 90% Effective Six Months After Final Dose
Moderna’s COVID-19 Vaccine 90% Effective Six Months After Final Dose

The vaccine was approved for emergency use in those aged 18 and older in December 2020 but with just two months of safety data.

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The new results come from its ongoing Phase 3 clinical trial involving more 30,000 people across the United States, and the headline efficacy figure is a slight decrease from an earlier figure of 94.1 percent published in the New England Journal of Medicine in December.

The new number is based on 900 adjudicated cases of COVID-19 from the study as of April 9, while the previous was based on 185 cases.

A company press release did not indicate why efficacy has fallen, but one reason might be the emergence of new variants of concern which are not as susceptible to antibodies evoked to the vaccine.

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Moderna is working on two variant-specific boosters, and said mice studies showed they elicited an increased immune response. The results of these studies have been posted online in a scientific paper that is now awaiting peer review.

“The new preclinical data on our variant-specific vaccine candidates give us confidence that we can proactively address emerging variants,” said CEO Stephane Bancel.

The company said that as of April 12, it has delivered 132 million doses of its vaccine globally, including approximately 117 million doses to the United States.

It remains on course to deliver its second tranche of 100 million doses by the end of May followed by 100 million more by the end of July.

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The company’s clinical trial for adolescents aged 12 to 17 is now fully enrolled with 3,000 US participants, and its pediatric trial for children aged six months to 11 years is continuing to enroll its 6,750 participants in the United States and China.

(AFP)

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