As of last night (Feb. 12) at 8:59 p.m., the Bloomberg COVID-vaccine tracker showed 50.1 million doses had been given and at a rate this past week 1.66 million doses a day.
The CDC vaccine tracker, updated last night (Feb. 12) at 8 p.m. showed slightly fewer doses administered: 48,410, 588 and 35,834,855 Americans as having received one dose and 12,085,830 as having received two.
The FDA has told Moderna it can add vaccine doses to each of its vials, the New York Times and other news outlets reported yesterday (Feb. 12). The newspaper said the company wants to increase the number of doses per vial from 10 to 14. Because Moderna is currently supplying about half of the vaccine in the U.S., the per-vial increase would translate into a 20% increase in the nation’s vaccine supply, the Times reported.
Neither the FDA nor Moderna had anything posted on their webistes this morning about the per-vial dose increase, although numerous media outlets have reported tha the company has talking to the FDA about the increase.
So far, the answer is a pretty emphatic no.
But Jon Cohen at Science reported yesterday (Feb. 12) that researchers are beginning to test whether getting a first shot of one type of COVID-19 vaccine and a second shot of a different type would be safe and effective. Mixing and matching might help vaccine shortages.
One mixed vaccine trial has started, according to the Cohen: the Sputnik V vaccine, made by Russia’s Gamaleya Research Institute of Epidemiology and Microbiology followed by a booster dose of the Oxford-AstraZeneca vaccine. A second trial of mix-and-match of Oxford-AstraZeneca vaccine with the Pfier-BioNTech jab is just getting going, Cohen reported, and and others are being talked abou.
The European Medicines Agency, which is Europe’s equivalent of the FDA, announced on Friday (Feb. 12) that has it has started a review of the RNA vaccine that has been developed by CureVac, a German biotech company.
The vaccine is still in clinical trials but a rolling review means the EMA will be looking at data as it comes in and presumably a quicker OK if the data shows safety and efficacy.
The CureVac jab is good company: The Moderna and the Pfizer-BioNTech vaccines are also RNA vaccines .
Some small European countries are losing patience with U.S. and Europen vaccine developers, so they are turning to China for COVID-19 vaccines, the Wall Street Journal is reporting this morning (Feb. 13). “The trend could increase China’s influence in the region as it campaigns to present itself as a reliable ally in fighting the coronavirus that was first detected on its soil,” the newspaper reported.
Hungary became the first EU member to separately authorize and buy vaccine from Sinopharm, a Chinese, state-owned company, WSJ reported.
Walmart, CVS, and Walgreens had websites up this week where you could register to get a COVID-19 vaccine shot. But when and where you could get a shot varied.
For example, this morning the Walgreens website indicated that a shot was available in the next three days within a 25-mile radius of an address in northwest St. Paul, Minnesota. But when an address in northwest Philadelphia (mine) was entered, no such luck.
CVS said on its website this morning that the vaccine was available at “select locations” in 18 states and Puerto Rico but not in 32 other states and in Washington, D.C.
President Joe Biden announced Thursday (Feb. 11) that the federal government had signed a contract with Modern and Pfizer more 100 million more doses of their vaccines. Those contracts, plus sooner delivery of other doses, mean that “we are not on track to have enough supply for 300 milloin Americans by the end of July,” Biden said in remarks delivered at NIH.
Children as young as first graders may be able to vaccinated against COVID-19 when the new school year starts in September, Anthony Fauci, M.D., director of the National Institute of Allergy and Infectious Diseases, said in an interview with ProPublica, investigative news website posted on Thursday (Feb.11)
“We’re in the process of starting clinical trials in what we call age de-escalation, where you do a clinical trial with people 16 to 12, then 12 to 9, then 9 to 6,” ProPublica quoted Fauci as saying in the piece that was posted on its website on Thursday (Feb. 11).
The White House announced on Tuesday (Feb.9) that federally qualified community health centers (FQHCs) will start getting their own direct supplies starting next week. The initial phase will include at least one center in each state, expanding to 250 centers in the coming weeks.
Differences in Defining “Clinically Meaningful” in Metastatic Breast Cancer Care
October 4th 2024Stephanie Graff, M.D., FACP, FASCO, director of breast oncology at the Lifespan Cancer Institute, explains the importance of the term “clinically meaningful” and shares some of the ways it can be defined.
Read More
In this latest episode of Tuning In to the C-Suite podcast, Briana Contreras, an editor with MHE had the pleasure of meeting Loren McCaghy, director of consulting, health and consumer engagement and product insight at Accenture, to discuss the organization's latest report on U.S. consumers switching healthcare providers and insurance payers.
Listen
In our latest "Meet the Board" podcast episode, Managed Healthcare Executive Editors caught up with editorial advisory board member, Eric Hunter, CEO of CareOregon, to discuss a number of topics, one including the merger that never closed with SCAN Health Plan due to local opposition from Oregonians.
Listen
Exploring Key Unmet Needs in Idiopathic Pulmonary Fibrosis
October 4th 2024Paul W. Noble, M.D., of Cedars-Sinai in Los Angeles, and Paul Frohna, M.D., Ph.D., of Endeavor BioMedicines, discussed the symptoms, epidemiology diagnosis and treatment of idiopathic pulmonary fibrosis (IPF) in a Managed Healthcare Executive K-Cast video series.
Read More