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The Vice Chairman of the Johnson Executive Committee
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The company will be the first to verify its candidate’s easiest regimen, developed through Janssen Pharmaceutical Companies, Dr. Dan Barouch, director of the Virology and Vaccine Research Center at Beth Israel Deaconess Medical Center, told FOX Business.
Although this is the fourth phase 3 of a coronavirus candidate in the United States after Moderna, Pfizer and AstraZeneca, J
OXFORD CORONAVIRUS VACCINE TRIAL, ASTRAZENECA SUMMARY
Phase 3 Together follows the “positive intermediate results” of the company’s Phase 1/2a clinical matrix “which demonstrated that the protection profile and immunogenicity after a singles vaccination led to additional development,” Johnson said.
Barouch, who leads the coronavirus vaccination effort in partnership with the pharmaceutical giant, notes that the effects were “necessary” before the next testing phase.
Preclinical knowledge has already indicated that “the company’s SARS-CoV-2 candidate vaccine generated a strong antibody reaction and coverage with a dose of singles,” said Dr. Paul Stoffels, Johnson’s chief scientific officer.
The pharmaceutical giant will now involve up to 60,000 adults from various backgrounds, adding a significant representation of the over-60s, to verify the effectiveness of the single vaccine dose.
PFIZER CEO SAYS CORONAVIRUS VACCINE COULD BE DISTRIBUTED TO THE UNITED STATES AT THE END OF THE YEAR
The trial will begin in the United States and then “quickly incorporate” into other countries, Barouch. Johnson said
“In order to compare the effectiveness of Janssen’s COVID-19 vaccine, countries and clinical trial sites that have a high incidence of COVID-19 and the ability to start up immediately will be activated,” the company said Wednesday.
While the first Phase 3 clinical trial will be based on a single injection diet, an upcoming trial will check a two-dose diet.
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So far, the candidate has also shown that it does not require a chain without frozen blood, it is shown to be solid for several months at refrigerator temperature, Barouch said.
“This will be a credit for the distribution of the vaccine,” he said, “if the vaccine ends up being effective. “
Barouch warned, however, that there is no transparent timetable on when the candidate will be in a position to be distributed.
“What is it is that the trials are aimed at the endpoints, which means there is no deadline to stop the review,” he said.
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Earlier this month, Johnson
Company CEOs have promised not to seek FDA approval, even for emergency use, until certain criteria are met.
If and when considered and effective, Johnson
The vaccine will also be provided to a “global non-profit base for use in the event of an emergency pandemic,” the pharmaceutical giant said in the past.
A manuscript containing all the knowledge related to the effects of the first phase 1/2a human clinical trial has been sent to medRxiv and is expected to be available online “soon,” Barouch said.
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Quotes displayed in real time or with delay of at least 15 minutes Market knowledge through Factset Developed and implemented through FactSet Digital Solutions Legal Statement. Knowledge of mutual funds and ETFs through Refinitiv Lipper.
This curtain must be posted, disseminated, rewritten or redistributed. © 2020 FOX News Network, LLC. All rights are reserved FAQs – Updated Privacy Policy