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There’s A New COVID Variant, KP.3 – These Are The Symptoms
IFLScience· 4 days agoKP.3 is one of the FLiRT variants of SARS-CoV-2. The immune system can learn to recognize spike...
Co-Diagnostics seeks FDA clearance for COVID-19 test By Investing.com
Investing.com· 5 days agoFood and Drug Administration (FDA) for its Co-Dx™ PCR Pro™ instrument and the Co-Dx PCR COVID-19...
FDA Tells Vaccine Makers to Target New COVID Variant for Fall
WFMZ Eastern Pennsylvania and Western New Jersey· 5 days agoFood and Drug Administration announced Thursday. It's a turnaround for the agency: The new...
FDA advises Covid vaccine makers to target new contagious strain for fall shots
NBC Universal via AOL· 6 days agoThe FDA advised drugmakers to update Covid vaccines to target the KP.2 strain, a descendant of the...
FDA recommends COVID jab manufacturers update formulas to combat new strain
BizPac Review· 4 days agoFDA) announced Thursday that manufacturers of the COVID vaccines should focus on the KP.2 strain of the JN.1 variant. “Based on the totality of the evidence ...
Moderna's (MRNA) Next-Gen COVID-19 Jab Study Meets Efficacy Goal
Zacks via Yahoo Finance· 5 days agoData from a late-stage study shows that Moderna's (MRNA) next-generation COVID-19 vaccine achieved...
...Phase 2b Clinical Study Evaluating the Company's Next-Generation COVID-19 Vaccine Candidate,...
NewMediaWire via Yahoo Finance· 1 day ago10,000-participant randomized Phase 2b study will evaluate and compare GeoVax's multi-antigen,...
FDA to vaccinemakers: Updated COVID shots should target KP.2 variant
Becker’s Hospital Review· 6 days agoThe FDA is now advising manufacturers to develop the 2024-2025 COVID-19 vaccines using the KP.2 strain for the formula, the agency announced ...
One Big, Unintended Consequence of the Failed Attempt to Ban the Abortion Pill
Slate via Yahoo News· 1 day agoNot until the waning days of the Obama administration did the FDA finally begin to relax some of the...
Co-Diagnostics Submits At-Home PCR System, COVID-19 Test to FDA
GenomeWeb News· 5 days agoCo-Diagnostics announced on Friday that it has submitted a PCR instrument and COVID-19 test to the US Food and Drug Administration for 510(k) clearance.