Biotech giant Moderna on Monday announced that its COVID-19 vaccine was 94.5% effective in preventing the disease during Phase 3 trials.

Moderna CEO Stéphane Bancel called it a “pivotal moment in the development of our COVID-19 vaccine candidate.”

“This positive interim analysis from our Phase 3 study has given us the first clinical validation that our vaccine can prevent COVID-19 disease, including severe disease,” he said in a statement.

Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, told CNN the results are “as good as it gets.” He told MSNBC that doses may start rolling out in December. Moderna said it expects to have 20 million doses ready to ship in the U.S. this year, and 500 to 1 billion globally in 2021.

The promising trial results follow last week’s news of Pfizer’s vaccine that showed a more than 90% efficacy rate. Both vaccines uses a vaccine production technology called mRNA, or messenger RNA.

Moderna’s coronavirus vaccine trial got its start at Seattle’s Kaiser Permanente Washington Health Research Institute. Members from Seattle’s tech community were part of the first group of participants to get their shots in the initial Moderna trials. The company last month completed enrolling 30,000 volunteers for its crucial Phase 3 trial.

The Dow was up more than 400 points on Monday morning. Shares of United Airlines and Uber rose, while Zoom and Peloton fell. Moderna’s stock was up more than 7%.

There are several other vaccines in development from companies including AstraZeneca, Johnson & Johnson, and Novavax. Fred Hutch last week opened volunteer enrollment for a Phase 3 study for AstraZeneca’s COVID-19 vaccine.

“We’re optimistic today about the success of the two mRNA vaccine candidates against COVID-19 and the other vaccine candidates in our testing pipeline, all of which target the SARS-CoV-2 spike protein,” Dr. Larry Corey, virologist at Seattle’s Fred Hutchinson Cancer Research Center and co-leader of the COVID-19 Prevention Network’s vaccine testing program, said in a statement Monday. “These results demonstrate that a single strand of RNA that transcribes a prefusion protein of the SARS CoV-2 virus, when wrapped in a lipid nanoparticle, can elicit a highly effective immune response in adults, among the elderly and across racial and ethnic populations.”

In the weeks ahead, clinical trials may progress far enough for the Food and Drug Administration to issue emergency use authorizations for promising vaccine candidates. But health experts at last month’s GeekWire Summit stressed that such an authorization would be only an interim step toward getting a vaccine widely distributed.

U.S. COVID-19 cases just topped 11 million. In Washington state, Gov. Jay Inslee on Sunday announced broad new restrictions on indoor gatherings, indoor dining, and more.

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