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Many local participants in Pfizer COVID-19 trial still double blinded

KINGSPORT â As the first rounds of the Pfizer COVID-19 vaccines are distributed to health care workers and nursing home residents, some local participants in the clinical trial are âanxiously waitingâ to find out if they got the vaccine or a placebo.
Most participants donât know for sure which of the two they received.
The vaccine has been given âemergency use authorizationâ but not yet FDA approval, so the participants are still part of an ongoing trial that is generating data for researchers.
Retired Eastman Chemical Co. chemist Bill Tindall said Monday that he and his wife, Judy, volunteered to participate in the Pfizer-BioNTech trial through Holston Medical Group after reading an Aug. 11 article in the Kingsport Times News that reported volunteers were needed. ....

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FDA Takes Key Action in Fight Against COVID-19 By Issuing Emergency Use Authorization for First COVI

FDA Takes Key Action in Fight Against COVID-19 By Issuing Emergency Use Authorization for First COVI
pharmiweb.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmiweb.com Daily Mail and Mail on Sunday newspapers.

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Vaccines and Related Biological Products Advisory Committee December 10, 2020 Meeting Announcement - 12/10/2020 - 12/10/2020

Agenda
The meeting presentations will be heard, viewed, captioned, and recorded through an online teleconferencing platform. On December 10, 2020, the Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session to discuss Emergency Use Authorization (EUA) of the Pfizer-BioNTech COVID-19 Vaccine for the prevention of COVID-19 in individuals 16 years of age and older.
Meeting Materials
FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its website prior to the meeting, any background material will be made publicly available at the time of the advisory committee meeting, and additional materials will be posted on FDA s website after the meeting. ....

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