A panel of outside advisers to the U.S. Food and Drug Administration is expected to endorse emergency use of Moderna Inc.’s coronavirus vaccine during a meeting...
Surface Oncology agreed to grant exclusive worldwide licensing rights to GlaxoSmithKline for the development and commercialization of the Cambridge, Mass.-based biotech company’s SRF813, a fully human...
As we hunker down this holiday season, waiting for our vaccines, or at least until the diffusion of the vaccines has slowed the spread of the...
Trials of a fifth COVID-19 vaccine have begun in the UK, as IT issues threaten to delay the The post Trials of Valneva COVID-19 vaccine begin...
BIOTRONIK won FDA clearance for the Vital Data Sensor, a body temperature component within the BIOMONITOR IIIm injectable cardiac monitor (ICM). The ICM is designed to...
Merck & Co. announced on Thursday that the US Food and Drug Administration (FDA) has granted priority review for the use of its lead drug Keytruda in...
A therapy to treat hyperphosphatemia is moving closer to the market after years of development by California-based company The post Ardelyx’s ambition to revolutionise kidney treatment...
BioNTech and Shanghai Fosun Pharmaceutical announced an agreement for the supply of an initial 100 million doses of their COVID-19 vaccine BNT162 to mainland China in...
While Pfizer and the US government are still negotiating for more doses of its BioNTech-partnered mRNA vaccine, the FDA has cleared the way for pharmacists to...
Abbott Laboratories has been granted Emergency Use Authorization (EUA) by the US Food and Drug Administration (FDA) for its virtually guided at-home BinaxNow COVID-19 Ag Card...
Trials of a fifth COVID-19 vaccine have begun in the UK, as IT issues threaten to delay the The post Trials of fifth COVID-19 vaccine begin...
Favorable COVID-19 vaccine developments have revived the hopes of several companies that have seen demand for their products crushed by the unprecedented pandemic. That said, the...
Lexicon Pharmaceuticals has entered into a collaboration agreement with AC Bioscience, enabling the use of preclinical and clinical data for LX2931, without granting any right or...
CNBC Transcript: Dr. Anthony Fauci speaks with CNBC ’s Meg Tirrell live during the CNBC Healthy Returns Livestream today and gives his predictions for coronavirus after...
Why The Number '3' May Make You Rethink The COVID Hysteria Tyler Durden Wed, 12/16/2020 - 13:52 Authored by Simon Black via SovereignMan.com, Yesterday I promised...
FDA Approves First Rapid At-Home COVID Test
Stocks rose sharply on Tuesday (Dec. 15) as optimism grew that Congress could pass another COVID stimulus package before year’s end. Q3 2020 hedge fund letters,...
A roundup of biopharma news and updates includes Merck and Eisai’s Keytruda-Lenvima combo hitting the mark in a Phase III study for advanced endometrial cancer.
As countries like the US, UK and Canada roll out the first doses of Pfizer and BioNTech’s Covid-19 vaccine, some worry it could be years before...
AbbVie is to begin clinical development of an antibody designed to neutralise the SARS-CoV-2 coronavirus after licensing the The post AbbVie begins trials of COVID-19 antibody...
Non-British Europeans may start receiving Covid-19 vaccinations sooner than originally planned. The EMA announced Tuesday that it had moved up an expert panel meeting on the...
Global Stocks Hit All Time High On Stimulus Optimism Ahead Of Fed Meeting Tyler Durden Wed, 12/16/2020 - 07:40 Another overnight session, and - predictably -...
Credit: BAT / KBP Investigational New Drug application approved by the FDA for COVID-19 candidate vaccine, allowing BAT to progress into a Phase I clinical trial...
Equity markets rise on stimulus hopes Equity markets shrugged off a previous run of losses, and the US dollar weakened overnight, despite weaker US data. Rising...
2020 saw some notable tech names opt for a public listing despite the COVID-19 disruptions. One such company is data analytics provider Palantir Technologies, which started...
Moderna looks odds on to claim emergency use authorisation from the FDA for its COVID-19 vaccine this week, The post FDA backs Moderna COVID-19 shot ahead...
The U.S. Food and Drug administration authorized emergency use of the first over-the-counter Covid-19 antigen test, which can be used at home.
Last week, Moderna (MRNA) kicked off its TeenCOVE Study, dosing the first participants in the Phase 2/3 trial of the company’s Covid-19 vaccine candidate mRNA-1273, in...
Gilead Sciences Inc. decided not to pursue the U.S. Food and Drug Administration’s approval of the company's experimental rheumatoid arthritis treatment, filgotinib, following a meeting with...
A SiriusXM Special Vaccine Edition on Doctor Radio featuring Admiral Brett Giroir MD, who discusses how many should get the vaccine by the end of year,...