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Market Extra: All eyes on Lagarde, as ECB meets following emergency interest rate cuts by Fed, Bank of England
The European Central Bank may be running low on firepower, but market volatility and falling inflation expectations tied to the COVID-19 outbreak provides growing pressure to act more aggressively than previously expected, analysts say......»»
Humanigen Shares Gain On FDA Emergency Filing Plans For COVID-19 Drug By June
Humanigen Inc (NASDAQ: HGEN) is prepping its COVID-19 drug lenzilumab for an emergency use authorization with the FDA before the month’s end. According to its Q1 financial report out Thursday after-ho.....»»
Pfizer-BioNTech COVID-19 Vaccine Gets FDA Emergency Approval For Age Group 12-15
The U.S. Food and Drug Administration on Monday approved the emergency use of Pfizer Inc. (NYSE: PFE) and BioNTech SE’s (NASDAQ: BNTX) COVID-19 vaccine in adolescents aged between 12 to 15 years. read more.....»»
FDA authorizes emergency use of Pfizer, BioNTech COVID vaccine to kids 12-15
The U.S. Food and Drug Administration late Monday authorized the emergency use of Pfizer Inc. and BioNTech SE COVID-19 vacccine for children between the age.....»»
: Four COVID-19 vaccines are being tested in children and teens. Here’s when different age groups could become eligible for shots.
The Food and Drug Administration is expected to grant emergency authorization to Pfizer's COVID-19 vaccine for 12- to 15-year-olds within the week. If that occurs, it will be the first shot authorized for this group of younger teens......»»
: Four COVID-19 vaccines are being tested in children and teens. Here’s when to expect a shot for different age groups
The Food and Drug Administration is expected to grant emergency authorization to Pfizer's COVID-19 vaccine for 12 to 15-year-olds within the week. If that occurs, it will be the first shot authorized for this group of teens......»»
Pfizer COVID-19 Vaccine Expected To Get FDA Emergency Approval For Age Group 12-15 Next Week
The Food and Drug Administration has plans to authorize the emergency use of Pfizer Inc (NYSE: PFE) and BioNTech SE's (NASDAQ: BNTX) jointly-developed COVID-19 vaccine in adolescents aged between 12 to 15 years, t read more.....»»
GlaxoSmithKline and Vir Biotech seek FDA emergency authorization for COVID antibody treatment
GlaxoSmithKline PLC and Vir Biotechnology Inc. said Friday they have submitted to the U.S. Food and Drug Administration an application for emergency use authorization for their antibody treatment for mild-to-moderate COVID-19 in adults and adolesce.....»»
: FDA authorizes the first single-dose COVID-19 vaccine
The Food and Drug Administration on Saturday granted emergency authorization to Johnson & Johnson's COVID-19 vaccine, making it the third vaccine to become available to Americans during the pandemic and the first to only require one dose......»»
Johnson & Johnson"s Vaccine Gets Unanimous Backing Of FDA Panel, Emergency-Use Authorization Soon To Come
Johnson & Johnson's (NYSE: JNJ) coronavirus vaccine candidate could be given clearance for emergency use today, following unanimous backing by a Food and Drug Administration panel. read more.....»»
FDA tells J&J it"s working on an emergency authorization for its COVID-19 vaccine
Shares of Johnson & Johnson gained 1.3% in after-hours trading on Friday after the Food and Drug Administration said it has contacted the company to say it is "rapidly" working toward issuing an emergency use authorization for J&J's COV.....»»
: J&J’s one-shot COVID-19 vaccine nears authorization as FDA has no ‘specific safety concerns’
The Food and Drug Administration said that Johnson & Johnson's single-dose COVID-19 vaccine candidate has no unexpected safety concerns, in a step that moves the experimental vaccine one step closer to emergency authorization......»»
FDA grants authorization to Lilly"s COVID-19 antibody treatment
Shares of Eli Lilly & Co. were up 1.1% in premarket trading on Wednesday, the day after the Food and Drug Administration granted emergency authorization to the company's.....»»
Johnson & Johnson Seeks US Emergency Approval For Single Dose COVID-19 Vaccine
Johnson & Johnson (NYSE: JNJ) said Wednesday that its subsidiary Janssen Biotech Inc is requesting approval from the United States Food and Drug Administration for its single-dose COVID-19 vaccine candidate. read more.....»»
A new coronavirus variant has been tied to at least 90 infections in a deadly outbreak at a medical center in San Jose, California
The variant, L452R, is different than another, more transmissible variant that w.....»»
Pakistan approves AstraZeneca"s COVID-19 vaccine for emergency use
Pakistan's drug regulators on Saturday approved the coronavirus vaccine developed by AstraZeneca and Oxford University for emergency use, say reports. A man and child with prote.....»»
An employer’s dilemma: to mandate (or not) the Covid-19 vaccine?
During a year in need of some brightness, December brought some great news: after emergency Food and Drug Administration approvals, first Pfizer and then Moderna shipped Covid-19 vaccines to locations throughout the United States, kicking off a ma.....»»
Walgreens says any gains from COVID-19 vaccine to be countered by lockdown-related losses
Walgreens Boots Alliance lost $308 million in its first fiscal quarter due to COVID-19 and a big charge tied to its drug wholesaler stake, but the company’s overa.....»»
Amazon is now selling an FDA-approved at-home saliva COVID-19 test for $110. All you do is spit in a tube and send it to an LA lab via pre-paid shipping.
Amazon is selling the first at-home saliva test to get emergency use authorization (EUA) from the Food and Drug Administration. Parcels are stored in a truck in a logistics centre of t.....»»
Economic Report: Jobless claims fall to 3-week low of 803,000, but still show more coronavirus layoffs
New applications for U.S. unemployment benefits fell to a three-week low of 803,000 right before Christmas, but the relatively high level still reflected a fresh wave of layoffs tied to the record outbreak in coronavirus cases......»»