Journal du Club des Cordeliers - Moderna announces positive results for Omicron vaccine

NYSE - LSE
RBGPF 0% 77.27 $
CMSC 0.33% 24.38 $
SCS 1.65% 17 $
BCC 3.53% 89.01 $
NGG 0.55% 71.07 $
RIO 0.7% 62.54 $
GSK 2.36% 41.48 $
BTI 1.83% 57.31 $
AZN 0.36% 81.1 $
RELX 2.59% 46.33 $
BCE 0.66% 24.3 $
RYCEF 1.65% 15.12 $
CMSD 0.21% 24.39 $
JRI 0.71% 14.12 $
VOD 1.77% 11.86 $
BP -0.84% 34.47 $
Moderna announces positive results for Omicron vaccine
Moderna announces positive results for Omicron vaccine / Photo: Joseph Prezioso - AFP

Moderna announces positive results for Omicron vaccine

US biotech company Moderna on Wednesday announced positive results for a new vaccine that targets both the original Covid strain and Omicron.

Text size:

This so-called "bivalent" vaccine was tested in a trial of more 850 adults, who had all received their first three doses of Moderna's original Spikevax vaccine.

Around half the group then received a fourth dose of Spikevax, while the rest received the bivalent vaccine.

Those who received the bivalent vaccine had significantly higher levels of neutralizing antibodies -- Y-shaped immune system proteins that block the virus -- against Omicron.

On average, these levels were around 75 percent higher in the group who got the bivalent vaccine as a fourth dose compared to those who got the original vaccine as a fourth dose. They also received slightly superior protection to the ancestral strain of Covid compared to Spikevax.

"We are thrilled," said Stephane Bancel, CEO of Moderna in a statement, adding he anticipated this vaccine would be the company's lead candidate for authorization as a booster this fall.

"We want to be as ready as early as August for shipping," he told investors in a call.

Stephen Hoge, the company's president, did concede that antibody levels would be lower against Omicron's sub variants that are now in circulation, but said he believed it was still a superior booster than repeating Spikevax.

The company doesn't yet have data on durability -- how the new vaccine booster will fare three months and six months out.

A panel of Food and Drug Administration experts will meet June 28 to discuss considerations and strategies for boosters in fall and winter.

F.Fabre--JdCdC