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New low cost Covid-19 vaccine developed in Texas gets approval for use in India

 

A new, low-cost Texas Children’s Hospital vaccine gets approval for use in India

A COVID-19 vaccine created at the Texas Children's Hospital Center for Vaccine Development in Houston has received emergency use authorization in India, after nearly 10 years of research and funding obstacles in 2020.

The goal is to make the vaccine – called Corbevax – available in other low- and middle-income nations across the globe to help prevent future variants of concern from forming.

“As long as we leave the southern hemisphere unvaccinated new variants of concern for us will emerge," said Dr. Peter Hotez, co-director of the Texas Children's Hospital Center for Vaccine Development and dean at Baylor's National School of Tropical Medicine. “The only way to stop it is to vaccinate the world and we think our [vaccine] is going to be a major contributor to that."

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Testing for Omicron may need re-evaluation--South African study

If confirmed in follow-up research and if the diagnostics industry can pivot quickly enough, findings from a South African study could make COVID-19 testing a lot easier for patients and healthcare workers, as the SARS-CoV-2 Omicron variant becomes the dominant source of infection.

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U.S. CDC shortens recommended Covid-19 isolation and quarantine time for infected persons without symptoms

(CNN) The US Centers for Disease Control and Prevention on Monday shortened the recommended times that people should isolate when they've tested positive for Covid-19 from 10 days to five days if they don't have symptoms -- and if they wear a mask around others for at least five more days.

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New COVID treatments are coming but wll they help combat omicron

Omicron is already changing how medicine fights COVID-19.

Although it only became widespread across the United States in the past week, doctors, pharmacists and drug companies said they need different tools against the new variant.

Two well-used monoclonal antibodies are unlikely to be effective against omicron. In their place, the government accelerated authorization of two antivirals that can be taken right after diagnosis to prevent illnesses from becoming severe.

The Food and Drug Administration on Wednesday authorized use of Pfizer's Paxlovid, a series of pills, taken at home that prevent nearly 90% of severe COVID-19 among those at high risk. On Thursday, the FDA authorized use of a second antiviral, molnupiravir, which appears to prevent progression to severe disease about 30% of the time.

"As we face omicron, the nation's medicine cabinet of treatments gives us more options to protect the American people," said Jeff Zients, the White House Coronavirus Response Coordinator. "We have tools to keep people safe and we will continue to use them."

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