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Tuesday, March 1, 2022

Pfizer Covid vaccine is less effective in kids 5 to 11, study finds

 Newly emerging data suggest the Pfizer-BioNTech Covid vaccine works substantially less well at preventing infection and hospitalizations in children aged 5 to 11 than it does in those aged 12 to 17 — a finding that is raising questions about whether the companies chose the wrong dose for the younger children.

The data, from New York state, show a rapid and substantial decline in protection after vaccination in children in the younger age group, with efficacy against infections dropping off more quickly and dramatically than the declines seen in children aged 12 to 17. The study also found a significant, but less steep, decline in protection against hospitalizations.

The findings, compiled by researchers working for the New York State Department of Health, were posted Monday on a preprint server; the study has not yet undergone peer review.

The New York findings, along with data from several other databases, were recently presented to the Covid vaccine work group of the Advisory Committee on Immunization Practices, independent vaccine experts who advise the Centers for Disease Control and Prevention, sources told STAT.

The data come on the heels of disappointing results from Pfizer trials of an even lower vaccine dose in children under the age of 5. And they will raise questions about whether, in trying to find doses that were both protective and tolerable in children, the companies failed to hit the mark for both age groups.

Pfizer would not say if it is exploring the possibility that the dose used in children might be too low, but said it is “confident in the protection and safety” of its Covid-19 vaccine.

“Our updates earlier this year on pursuing a 3-dose schedule for the pediatric population were informed by the effectiveness data for three doses of the vaccine for people 16 years and older, and the early laboratory data observed with Delta and other variants of concern, including Omicron, which suggest that people vaccinated with three doses of a Covid-19 vaccine may have a higher degree of protection,” it said in an emailed statement.

But John Moore, a virologist at Weill Cornell Medical College, said given the findings of this study, it’s hard to see how the lower efficacy in children aged 5 to 11 could be due to anything but the lower dose they received. In the study, children aged 12 had the highest vaccine efficacy of all age groups in both cohorts.“The striking difference between 11- and 12-year-olds can only be explained by the three-fold dosing reduction in the younger children. The one-year age difference is highly unlikely to make any other factor relevant,” Moore said by email. “The 11-year-olds got the 3-fold reduced dose, the 12-year-olds the standard dose.”

The New York study analyzed health records for Covid cases in children and teens from Dec. 13, 2021 to Jan. 30, 2022, a period during which the Omicron variant was fast replacing all other forms of the SARS-CoV-2 virus in the country. Covid vaccines are not as protective against Omicron as they were against earlier versions of the virus, especially without a booster shot.

The state recorded more than 850,000 Covid cases in adolescents aged 12 to 17 during that time, and about 365,000 in children aged 5 to 11.

Over that period, two-dose vaccine protection against infection for kids aged 5 to 11 declined from 68% to 12%; the vaccine’s effectiveness at preventing hospitalization declined from 100% to 48%.

But two-dose protection against infection for children aged 12 to 17 only dropped from 66% to 51%, and protection against hospitalization from 85% to 73%.

“Our data support vaccine protection against severe disease among children 5-11 years, but suggest rapid loss of protection against infection, in the Omicron variant era,” the researchers wrote. “Should such findings be replicated in other settings, review of the dosing schedule for children 5-11 years appears prudent.”

The adult Pfizer regimen — used in anyone aged 12 and older — is two doses of 30 micrograms apiece, given 21 days apart. Children 5 to 11 years old receive a dose that is one-third that size, two doses of 10 micrograms apiece. And in studies of children under 5, the dose is further reduced, with the children aged 6 months to 4 years getting two 3-microgram doses. The vaccine is not yet authorized for use in children under 5.

In December, Pfizer announced that two doses of the vaccine in children under 5 had not generated the same level of antibodies as was seen after two doses in people 16 to 25, which was being used as a proxy for protection. It said it would give the children under 5 a third dose to see if that achieved the required level of protection.

But then as Omicron cases spiked across the country, the Food and Drug Administration revealed it was considering a rolling authorization for the vaccine for children under age 5, allowing parents to start vaccinating their children while waiting for the third dose. The rationale was that the risk-benefit equation had shifted with Omicron.

A meeting of the FDA’s vaccine advisers, the Vaccines and Related Biological Products Advisory Committee, was scheduled for mid-February. But before the group could meet the FDA and Pfizer announced the plan was on hold. The plan is now to wait for the third-dose results before considering authorization in this age group.

https://www.statnews.com/2022/02/28/pfizer-covid-vaccine-kids-5-11/

New Mexico bill allows testing to prevent fentanyl deaths

 New Mexico is allowing broad access to test strips that can detect the presence of the potent opiate fentanyl and potentially help avoid deadly overdoses, under legislation signed Monday by Democratic Gov. Michelle Lujan Grisham.

The bill from Democratic legislators in Albuquerque, Santa Fe and Los Alamos lifts restrictions on public access to devices that can test for drug impurities. It also gives state health health officials new authority to intervene and rein in the spread of diseases like HIV and hepatitis that can be transmitted through intravenous drug use.

Overdoses in New Mexico increasingly are linked to the ingestion of drugs laced with fentanyl. States including Arizona already have decriminalized test strips designed to detect fentanyl.

New Mexico routinely leads the American West in rates of opioid-related drug overdose deaths. It also has been on the forefront of strategies to reduce the toll of drug use and addiction, from the distribution of overdose antidote drugs to legal immunity provisions for people who may implicate themselves in crimes by seeking overdose treatment for themselves or others.

https://apnews.com/article/business-health-new-mexico-albuquerque-santa-fe-dc44c1be7a0657580cfb1f17c2c9de44

Monday, February 28, 2022

Bayer Beat Expectations in 4Q; Guides for Increased Earnings, Sales in 2022

 Bayer AG on Tuesday posted earnings and sales that beat consensus expectations, and guided for increased earnings and sales in the year ahead.

The German pharmaceutical-and-agricultural company reported net profit of 1.16 billion euros ($1.30 billion) for the last quarter of the year, up from EUR308 million in the same quarter the year prior and beating analysts' expectations of EUR731 million.

Earnings before interest, taxes, depreciation and amortization before special items came in at EUR2.40 billion, also up from the previous year, when it was EUR2.39 billion.

Sales grew to EUR11.12 billion from EUR10 billion the year prior, beating consensus expectations of EUR10.47 billion.

Looking ahead, the company said it expects to significantly increase sales, earnings and free cash flow in 2022. Sales are expected to be about EUR46 billion in the year ahead, while Ebitda before special items should be about EUR12 billion, Bayer said.

Core earnings per share are expected to be about EUR7, while free cash flow is seen at about EUR2 billion to EUR2.5 billion, after deducting settlement payments.

Bayer said it would propose to maintain its dividend unchanged to EUR2.

https://www.marketscreener.com/quote/stock/BAYER-AG-436063/news/Bayer-Beat-Expectations-in-4Q-Guides-for-Increased-Earnings-Sales-in-2022-39618912/

Glaxo: Daprodustat Drug Gets EU Marketing Authorization

 GlaxoSmithKline PLC said Tuesday that its drug Daprodustat has received marketing authorization by the European Medicines Agency.

The company said its application was accepted for review by the EMA.

The drug Daprodustat, aimed at treating anaemia of chronic kidney disease, is currently approved in Japan, the FTSE 100-listed company said.

https://www.marketscreener.com/quote/stock/GLAXOSMITHKLINE-PLC-9590199/news/GlaxoSmithKline-Says-Daprodustat-Drug-Gets-EU-Marketing-Authorization-39619011/

AstraZeneca, Neurimmune Sign Exclusive Commercialization Global Deal

 AstraZeneca PLC said Tuesday that its rare disease group Alexion has closed an exclusive global deal and license agreement with Neurimmune AG to commercialize NI006, an investigational antibody in Phase 1b aimed at treating a cardiomyopathy.

The Anglo-Swedish pharma giant said that Alexion has agreed to make an upfront payment to Neurimmune of $30 million, adding that Neurimmune will continue to be responsible to complete the current phase of the trial while Alexion pays certain trial costs.

"Alexion will make additional contingent milestone payments of up to $730 million upon achievement of certain development, regulatory and commercial milestones. It will also pay low-to-mid teen royalties on net sales of any approved medicine resulting from the collaboration," the FTSE 100 listed company said.

https://www.marketscreener.com/quote/stock/ASTRAZENECA-PLC-4000930/news/AstraZeneca-Neurimmune-Sign-Exclusive-Commercialization-Global-Deal-39619154/

Poison Control Centers Warn About Toxic Chemical In At-Home COVID-19 Test Kits

 by Jack Phillips via The Epoch Times (emphasis ours),

Some at-home rapid COVID-19 tests contain a toxic chemical that may be harmful to both children and adults, according to health officials.

A Flowflex COVID-19 Lateral Flow (LFT) self-test kit, containing a SARS-CoV-2 Antigen Rapid Test, arranged for a photograph, in London on Feb. 20, 2022. (Justin Tallis/AFP via Getty Images)

The Cincinnati Drug and Poison Information Center reported an uptick in accidental exposures to a possibly toxic substance in at-home COVID-19 test kits, according to a blog post. Meanwhile, the National Poison Control Center issued a warning about the chemical.

“It is important to know that the extraction vial in many rapid antigen kits includes the chemical sodium azide as a preservative agent,” the center said. “The BinaxNow, BD Veritor, Flowflex, and Celltrion DiaTrust COVID-19 rapid antigen kits all contain this chemical.”

Sodium azide is a colorless, odorless powder that testers dip cotton swabs into. The chemical is found in herbicides, pest control agents, and airbags for cars.

Small doses of sodium azide can lower blood pressure, and larger doses may cause more serious health effects,” an advisory from Health Canada also said. “ProClin is also found in many kits. It contains chemicals that can cause skin and eye irritation, as well as allergic reactions.”

Some hospitals around the United States say they have received a surge in phone calls about exposures to the chemical.

“We started getting our first exposures to these test kits around early November,” said Sheila Goertemoeller, pharmacist and clinical toxicologist for the Cincinnati Children’s Hospital Medical Center. “It was, really, all ages.”

“Mostly, I’ve been very worried about our young children.”

Accidental exposure is occurring among both children and adults, said Dr. Kelly Johnson-Arbor, with the National Capital Poison Center in Washington, told WNEP over the weekend.

“People might mistake them for eye drops. Children might drop it onto their skin. Adults will sometimes mistakenly put them into their eyes,” she said.

“You don’t want to leave it on the skin because it could potentially cause an allergic reaction or a skin rash.

If someone drinks the solution, it’s really important to contact poison control right away. The solutions have different ingredients. Some have non-toxic ingredients and others have more dangerous ingredients.”

Officials told WNEP that there’s no need to throw away the test kits, but people should be mindful when using them.

“Use them properly, dispose of them properly, and it won’t cause an issue,” Dr. Jeffrey Jahre, with St. Luke’s University Health Network, told the outlet.

If you suspect you or someone you know has ingested the chemical, officials recommend not to make the person vomit. For eye exposures, rinse the eyes for 15 to 20 minutes with warm water. For skin exposures, rinse the skin well with tap water. Immediately check the Poison Control Center’s online tool for guidance or call poison control at 1-800-222-1222, the website says.

https://www.zerohedge.com/covid-19/poison-control-centers-warn-about-toxic-chemical-home-covid-19-test-kits

Breakthrough gene-editing technology belongs to Harvard, MIT -U.S. tribunal

 A U.S. tribunal overseeing patent disputes ruled on Monday that patents on the breakthrough gene-editing technology known as CRISPR belong to Harvard University and the Massachusetts Institute of Technology.

The U.S. Patent and Trademark Office's decision is a defeat for the University of California, Berkeley; the University of Vienna and Nobel Prize-winning researcher Emmanuelle Charpentier.

Harvard's and MIT's Broad Institute, which obtained the first CRISPR patent in 2014 and later obtained related patents, said the decision confirmed its patents were properly issued.

CRISPR lets scientists edit genes by using biological scissors that can edit DNA.

The technology is being tested in clinical trials to potentially help cure diseases caused by genetic mutations and abnormalities.

Jennifer Doudna of UC Berkeley and Charpentier of the University of Vienna had been first to seek a CRISPR patent in 2012. Eight years later they shared the Nobel Prize in Chemistry for their CRISPR work.

https://www.userwalls.com/n/breakthrough-gene-editing-technology-belongs-harvard-mit-tribunal-2888460/