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Vaccinating young children against Covid-19 may be more challenging this respiratory virus season

Vaccinating young children against Covid-19 may be more challenging this respiratory virus season

CNN2 days ago
Parents in the United States who want to vaccinate their young children against Covid-19 may face a growing set of challenges this fall.
The US Food and Drug Administration might not renew authorization for Pfizer's Covid-19 vaccine for children younger than 5, the US Centers for Disease Control and Prevention told state and local health officials on Friday.
'This decision would affect Pfizer's pediatric COVID-19 vaccine for children aged 6m–4y for the 2025–2026 season,' the CDC's National Center for Immunization and Respiratory Diseases said in an email that was obtained by CNN.
In May, US Health and Human Services Secretary Robert F. Kennedy Jr. announced that the CDC would no longer recommend Covid-19 vaccines for healthy children or pregnant women. The CDC's immunization schedule was updated to reflect that children would be able to get the vaccines after consulting with a health care provider — what's known as 'shared decision-making.'
But without FDA authorization, Pfizer's Covid-19 vaccine would no longer be available to any children younger than 5 and the other option available for healthy children with no underlying conditions in this age group, Moderna's Covid-19 vaccine, would have to be given 'off label' by a willing pharmacist or physician.
This contradicts the intent of shared clinical decision-making, said Dr. Paul Offit, a pediatrician and director of the Vaccine Education Center at Children's Hospital of Philadelphia.
'Shared clinical decision-making assumes that you're making a decision for that child whether they're healthy or not healthy. So now it's confusing,' he said.
Covid-19 vaccines first became available to the American public during the pandemic under emergency use authorization, known as EUA — special permissions used by the FDA during an emergency that are short of full approval.
Pfizer has had full FDA approval for its Covid-19 vaccine for individuals age 12 and older since 2022. The company anticipates that this approval will expand to children ages 5 to 11 for the upcoming respiratory virus season, according to the email that the CDC's National Center for Immunization and Respiratory Diseases sent to state and local health officials on Friday.
But vaccine access for the youngest children, who are most vulnerable to severe illness from a Covid-19 infection, would be significantly more limited if the FDA does not renew emergency authorization for the Pfizer vaccine for children under 5.
Pfizer confirmed to CNN that the FDA has said that it may not renew the emergency use authorization or the Pfizer-BioNTech Covid-19 vaccine for children ages 6 months to 4 years.
'We are currently in discussions with the agency on potential paths forward and have requested that the EUA for this age group remain in place for the 2025-2026 season,' Pfizer said in a statement. 'It is important to note that these deliberations are not related to the safety and efficacy of the vaccine which continues to demonstrate a favorable profile.'
Fatima Khan, co-founder of the nonprofit grassroots group Protect Their Future, which advocates for vaccine access for kids, told CNN in a statement, that 'taking a proven, safe and effective vaccine away from vulnerable children is unconscionable.'
'The science is clear: Infants face Covid-19 hospitalization rates comparable to those over 65. Refusing to authorize it for children under 5 doesn't protect them–it abandons them,' she said. 'Parents have already struggled to safeguard their youngest because of limited vaccine access. Now that protection may disappear entirely this fall just as schools reopen. If this stands, it will be a lasting stain on our public health system and on every leader who left our children behind.'
Moderna also has a Covid-19 vaccine available for children age 11 and younger. It was granted full approval by the FDA in July but only for those who are at 'increased risk for COVID-19 disease.'
Moderna plans to increase vaccine supply for children to 'help mitigate any potential supply gap,' according to the CDC email sent on Friday, but Moderna is still determining the specific volume and timing.
Like flu vaccines, Covid-19 vaccines have typically been updated with formulations that best target the virus strains that are in circulation each season. But the FDA has not yet approved the formulation for the 2025-2026 season.
'I think the bottom line is that children are going to be less likely to get this vaccine, which goes against the data,' Offit said.
At a meeting in April, the CDC's vaccine advisory committee heard evidence that children accounted for about 4% of all Covid-19 hospitalizations over last fall and winter's respiratory virus season.
Rates of Covid-19 hospitalizations among children are highest for the youngest age groups, CDC data shows. Last respiratory virus season, there were 48 Covid-19 hospitalizations for every 100,000 children under 5 – nearly seven times the rate for older children and more than twice the rate for adults under 50.
'It's a war on mRNA vaccines. Why? Because mRNA vaccines are now political,' Offit said. 'It's just a war against the science, war against the data, and we will suffer this. And the thing that I fear the most is: Will we know we're suffering this? Will we have the surveillance capacity to know who's getting hospitalized with Covid, who's dying from Covid?'
Covid-19 levels are on the rise in the US, with transmission increasing in at least 45 states, according to the CDC.
In a statement to CNN, the US Department of Health and Human Services said that the agency does not comment on potential regulatory changes.
'The COVID-19 pandemic ended with the expiration of the federal public health emergency in May 2023,' spokesperson Andrew Nixon said in an email. 'Unless officially announced by HHS, discussion about future agency action should be regarded as pure speculation.'
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Fall vaccines: Here's what you need to know about COVID, flu and RSV shots
Fall vaccines: Here's what you need to know about COVID, flu and RSV shots

Boston Globe

time5 minutes ago

  • Boston Globe

Fall vaccines: Here's what you need to know about COVID, flu and RSV shots

Amid uncertainty at the federal level, the Globe spoke with experts to guide readers on which vaccines are available, what doctors are recommending, and where to find reliable sources of information. Related : Advertisement COVID-19 Though the CDC's Advisory Committee on Immunization Practices has yet to officially weigh in on the COVID-19 vaccine, Kennedy While the Advertisement The Food and Drug Administration is also weighing whether to revoke its The American Academy of Pediatrics continues to recommend that all children starting at six months receive the COVID vaccine, even if they're healthy, Anders Pring said. According to Anders Pring recommends every child starting at age six months receive the 'primary series,' the two initial doses. For older children, Anders Pring recommends getting an annual booster, just like the flu shot. Naima Joseph, a maternal fetal medicine specialist at Boston Medical Center, recommends pregnant patients also receive the COVID-19 vaccine. Insurance companies are mandated to cover ACIP's recommendations. But since the panel's final recommendation has not been released, insurance companies have promised to accept the guidance from medical societies, Joseph said. 'We are hopeful that given AHIP has stated an intent to continue coverage of vaccines, it won't be a problem,' Joseph said. 'We will continue to partner with clinicians, pharmacists, community health workers to ensure equitable distribution of vaccines.' Advertisement Influenza The CDC still recommends the flu vaccine for everyone six months and older. But, in late June, Kennedy approved the CDC advisory committee's recommendation to Thimerosal, a mercury-based chemical compound, is used like a preservative in multi-dose vials. The ingredient has long been pushed by the anti-vaccine movement as being connected to autism, though that The move should not affect the supply of flu vaccines, doctors said, as thimerosal is used in less than 5 percent of U.S. flu vaccinations. Manufacturers Boston Medical Center is 'proactive in looking at supply chains throughout the year to ensure that we have sufficient stock,' said Cassandra Pierre, an infectious disease physician there. RSV Respiratory syncytial virus, which causes infections of the lungs and respiratory tract, primarily infects young children under 2 years old. It also impacts the elderly, especially those with weakened immune systems and chronic lung conditions. RSV infections are As of Aug. 4, the CDC In June, the federal panel approved a recommendation for Advertisement For pregnant women, the CDC recommends a single dose of the maternal RSV vaccine — in particular, Pfizer's Abrysvo — during weeks 32 through 36 of pregnancy. The RSV vaccine given to mothers allows antibodies to be passed to the baby before birth. Doctors agree that RSV vaccines are recommended for these populations. Pneumonia Pneumonia vaccines are available throughout the year, Pierre said. The It also recommends it for individuals who have underlying health conditions that put them at high risk for severe disease. That includes people with HIV, asthma or significant pulmonary disease, or diabetes, according to Pierre. Where can I find reliable information about vaccines? Pierre said guidance from professional organizations, like the American Academy of Pediatrics and the American Medical Association, are resources to look to. She added state and local boards for public health are 'wonderful unsung gems.' The While such resources exist, doctors ultimately urged patients to consult with their own clinicians. 'From a public health perspective, we as pediatricians love to talk with our patients and work with them,' Anders Pring said. Advertisement Jessica Ma can be reached at

BrainStorm Cell Therapeutics Announces Second Quarter 2025 Financial Results and Provides Corporate Update
BrainStorm Cell Therapeutics Announces Second Quarter 2025 Financial Results and Provides Corporate Update

Yahoo

timean hour ago

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BrainStorm Cell Therapeutics Announces Second Quarter 2025 Financial Results and Provides Corporate Update

Conference call and webcast scheduled for 8:30 a.m. Eastern Time Today, Thursday, August 14, 2025 NEW YORK, Aug. 14, 2025 /PRNewswire/ -- BrainStorm Cell Therapeutics Inc. (OTCQB: BCLI), a leading developer of adult stem cell therapeutics for neurodegenerative diseases, today announced financial results for the second quarter ended June 30, 2025, and provided a corporate update. "BrainStorm remains focused on executing our clinical development plan for NurOwn®. We reached an important milestone in Q2 with FDA clearance to initiate our Phase 3b trial, designed to generate confirmatory data to support a potential BLA submission," said Chaim Lebovits, President and CEO. "We are also advancing key operational activities, including discussions with clinical sites as well as ongoing engagement with our selected CDMO partners to ensure readiness for clinical drug supply. We are encouraged by the ongoing interest and support from clinicians and the ALS community, and we remain confident that, if approved, NurOwn has the potential to make a meaningful difference for patients and their families." Mr. Lebovits continued, "We support the FDA's consideration of the Citizen Petition, which may provide a fresh opportunity for an objective evaluation of the scientific evidence. We continue to stand behind the integrity and rigor of our data and will continue to engage with clinicians and the ALS community." Recent Highlights NurOwn (MSC-NTF) for ALS FDA has cleared the company to initiate the Phase 3b clinical trial of NurOwn® The Phase 3b trial, known as ENDURANCE, is expected to enroll approximately 200 participants at leading academic medical centers and will consist of a 24-week randomized, double-blind, placebo-controlled phase, followed by a 24-week open-label extension in which all participants will receive NurOwn. The primary endpoint is the change from baseline to week 24 in the ALS Functional Rating Scale-Revised (ALSFRS-R). Successful completion of the double blind portion of the study (Part A) is expected to generate the clinical data needed to support a new BLA submission. Details of the trial, including a list of anticipated participating clinical sites, are available on ID NCT06973629. A Citizens Petition submitted to the FDA by ALS Community requesting a new review of the NurOwn data The company acknowledges that the FDA's consideration of the petition provides a new opportunity to reaffirm NurOwn's potential as a therapy for ALS. BrainStorm was not involved in drafting or submitting this petition or its contents. New survival data from NurOwn Expanded Access Program show that 100% of participants (10/10) in the EAP survived more than 5 years from the onset of ALS symptoms, compared to published estimates indicating that approximately 10% of individuals with ALS would survive beyond 5 years. The single death in the cohort occurred following elective euthanasia. The median survival observed in the EAP cohort was 6.8 years (range: 6 to 7 years) from symptom onset. Although the EAP cohort included participants earlier in their disease course, these results are encouraging and support further study. Manufacturing Partnership with Minaris BrainStorm has signed a Letter of Intent (LOI) with Minaris Advanced Therapies, a global contract development and manufacturing organization (CDMO) specializing in cell and gene therapies, to manufacture NurOwn for the upcoming Phase 3b clinical trial. NurOwn® data selected as Breakthrough Science for Presentation at ISCT 2025 Meeting The new pharmacogenomic data were delivered in an oral presentation at the International Society for Cell & Gene Therapy (ISCT) 2025 Annual Meeting in May 2025, in New Orleans. The data highlight the impact of the UNC13A genotype on clinical outcomes for ALS patients treated with NurOwn. The presentation was featured in the ISCT public announcement regarding the meeting, which indicated that the data were "carefully reviewed and selected by the ISCT 2025 Planning Faculty, to explore the latest breakthroughs in the clinical translation of Mesenchymal Stem/Stromal Cells and how they will shape the future of cell therapies." Financial Results for the Second quarter Ended June 30, 2025 Cash, cash equivalents, and restricted cash were approximately $1.03 million as of June 30, 2025. Research and development expenditures, net, for the quarter ended June 30, 2025 were $1.1 million, compared to $0.9 million for the quarter ended June 30, 2024. General and administrative expenses for the quarter ended June 30, 2025 were approximately $1.4 million, compared to approximately $2.1 million for the quarter ended June 30, 2024. Net loss for the quarter ended June 30, 2025, was approximately $2.9 million, as compared to a net loss of approximately $2.5.4 million for the quarter ended June 30, 2024. Net loss per share for the three months ended June 30, 2025, and 2024 was $0.34 and $0.60, respectively. Conference Call and Webcast Participant Numbers: Toll Free 877-545-0320 International 973-528-0002 Participant Access Code 601260 Webcast The replay of the conference call can be accessed by dialing the numbers below and will be available until August 28. Replay Numbers: Toll Free 877-481-4010 International 919-882-2331 Reply Passcode 52831 About NurOwn® The NurOwn® technology platform (autologous MSC-NTF cells) represents a promising investigational therapeutic approach to targeting disease pathways important in neurodegenerative disorders. MSC-NTF cells are produced from autologous, bone marrow-derived mesenchymal stem cells (MSCs) that have been expanded and differentiated ex vivo. MSCs are converted into MSC-NTF cells by growing them under patented conditions that induce the cells to secrete high levels of neurotrophic factors (NTFs). Autologous MSC-NTF cells are designed to effectively deliver multiple NTFs and immunomodulatory cytokines directly to the site of damage to elicit a desired biological effect and ultimately slow or stabilize disease progression. About BrainStorm Cell Therapeutics Inc. BrainStorm Cell Therapeutics Inc. (OTCQB: BCLI) is a leading developer of autologous adult stem cell therapies for debilitating neurodegenerative diseases. The company's proprietary NurOwn® platform uses autologous mesenchymal stem cells (MSCs) to produce neurotrophic factor-secreting cells (MSC-NTF cells), designed to deliver targeted biological signals that modulate neuroinflammation and promote neuroprotection. NurOwn® is BrainStorm's lead investigational therapy for amyotrophic lateral sclerosis (ALS) and has received Orphan Drug designation from both the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). A Phase 3 trial in ALS (NCT03280056) has been completed, and a second Phase 3b trial is set to launch under a Special Protocol Assessment (SPA) agreement with the FDA. The NurOwn clinical program has generated valuable insights into ALS disease biology, including pharmacogenomic response associated with the UNC13A genotype, biomarker data collected at seven longitudinal time points, and a comprehensive analysis of the "Floor Effect" — a critical challenge in measuring clinical outcomes in advanced ALS. BrainStorm has published its findings in multiple peer-reviewed journals. In addition to ALS, BrainStorm has completed a Phase 2 open-label multicenter trial (NCT03799718) of MSC-NTF cells in progressive multiple sclerosis (MS), supported by a grant from the National MS Society. BrainStorm is also advancing a proprietary, allogeneic exosome-based platform designed to deliver therapeutic proteins and nucleic acids. The company recently received a Notice of Allowance from the U.S. Patent and Trademark Office for a foundational patent covering its exosome technology, further strengthening BrainStorm's growing IP portfolio in this emerging area of regenerative medicine. To learn more, visit Notice Regarding Forward-Looking Statements This press release contains "forward-looking statements" that are subject to substantial risks and uncertainties, including statements regarding meetings with the U.S. Food and Drug Administration (FDA), Special Protocol Assessment (SPA), the clinical development of NurOwn as a therapy for the treatment of ALS, the future availability of NurOwn to patients, and the future success of BrainStorm. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as "anticipate," "believe," "contemplate," "could," "estimate," "expect," "intend," "seek," "may," "might," "plan," "potential," "predict," "project," "target," "aim," "should," "will" "would," or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on BrainStorm's current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. These potential risks and uncertainties include, without limitation, management's ability to successfully achieve its goals, BrainStorm's ability to raise additional capital, BrainStorm's ability to continue as a going concern, prospects for future regulatory approval of NurOwn, whether BrainStorm's future interactions with the FDA will have productive outcomes, and other factors detailed in BrainStorm's annual report on Form 10-K and quarterly reports on Form 10-Q available at These factors should be considered carefully, and readers should not place undue reliance on BrainStorm's forward-looking statements. The forward-looking statements contained in this press release are based on the beliefs, expectations, and opinions of management as of the date of this press release. We do not assume any obligation to update forward-looking statements to reflect actual results or assumptions if circumstances or management's beliefs, expectations or opinions should change, unless otherwise required by law. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance, or achievements. CONTACTS Investors:Michael WoodPhone: +1 646-597-6983mwood@ Media: Uri Yablonka, Chief Business OfficerPhone: +1 917-284-2911uri@ CELL THERAPEUTICS INC. AND SUBSIDIARIES INTERIM CONDENSED CONSOLIDATED BALANCE SHEETS U.S. dollars in thousands (Except share data) June 30,December 31, 20252024 UnauditedAudited U.S. $ in thousands ASSETSCurrent Assets: Cash and cash equivalents$ 824$ 187 Other accounts receivable 106 63 Prepaid expenses and other current assets 585 135 Total current assets$ 1,515$ 385Long-Term Assets: Prepaid expenses and other long-term assets $ 24$ 22 Restricted Cash 201 184 Operating lease right of use asset (Note 3) 495 807 Property and Equipment, Net 331 434 Total Long-Term Assets$ 1,051$ 1,447Total assets$ 2,566$ 1,832LIABILITIES AND STOCKHOLDERS' EQUITY (DEFICIT)Current Liabilities: Accounts payables$ 5,997$ 6,080 Accrued expenses 367 619 Short-term loans (Note 7) 101 300 Operating lease liability (Note 3) 381 549 Employees related liability 1,682 1,430 Total current liabilities$ 8,528$ 8,978Long-Term Liabilities: Operating lease liability (Note 3) 95 171 Warrants liability (Note 4) - 447 Total long-term liabilities$ 95$ 618Total liabilities$ 8,623$ 9,596Stockholders' Deficit: Stock capital: (Note 5) 16 14 Common Stock of $0.00005 par value - Authorized: 250,000,000 shares at June 30, 2025 and at December 31, 2024 respectively; Issued and outstanding: 10,120,109 and 6,141,762 shares at June 30, 2025 and December 31, 2024 respectively Additional paid-in-capital 226,446 218,974 Treasury stocks (116) (116) Accumulated deficit (232,403) (226,636) Total stockholders' deficit$ (6,057)$ (7,764)Total liabilities and stockholders' deficit$ 2,566$ 1,832 BRAINSTORM CELL THERAPEUTICS INC. AND SUBSIDIARIES INTERIM CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS (UNAUDITED) U.S. dollars in thousands (Except share data) Six months ended Three months ended June 30, June 30, 2025202420252024 UnauditedUnaudited Operating expenses:Research anddevelopment, net$ 2,424$ 1,883$ 1,120$ 922 General and administrative 3,238 3,573 1,453 2,060Operating loss (5,662) (5,456) (2,573) (2,982)Financial income (expense), net (284) 43 (330) 30Gain (loss) on change in fair value of Warrants liability (Note 4) 179 529 - (411)Net loss$ (5,767)$ (5,942)$ (2,903)$ (2,541)Basic and diluted net lossper share from continuing operations$ (0.77)$ (1.35)$ (0.34)$ (0.60)Weighted average numberof shares outstanding usedin computing basic and diluted net loss per share 7,487,495 4,531,801 8,620,400 4,747,699 Logo - View original content to download multimedia: SOURCE BrainStorm Cell Therapeutics Inc.

Whoop there it is: FDA wants to regulate wearable firm's blood pressure tool
Whoop there it is: FDA wants to regulate wearable firm's blood pressure tool

Boston Globe

time2 hours ago

  • Boston Globe

Whoop there it is: FDA wants to regulate wearable firm's blood pressure tool

Get Starting Point A guide through the most important stories of the morning, delivered Monday through Friday. Enter Email Sign Up But in a response sent Aug. 4, Whoop rejected the FDA's assessment, saying the software didn't meet the definition of a medical device and the company would continue to offer the feature to users. The company, which shared the letter with The Boston Globe, also argued the move went against the goals of the Trump administration. Advertisement 'Seeking to regulate the feature as a medical device also runs counter to the stated policy of the Secretary of the Department of Health and Human Services, Robert F. Kennedy Jr., of 'clearing away regulatory barriers so innovation can thrive,'' Whoop said in the letter. Advertisement Whoop's refusal to comply with the FDA's request is uncommon, legal experts said. The FDA, which oversees the safety of medical devices and pharmaceuticals, is usually the ultimate decider of what comes under its jurisdiction and which devices can be sold to help people manage or treat health conditions. Chris Robertson, a Boston University law professor who teaches FDA law, said any communication from the FDA to a company is typically enough to make the company get in line with federal standards. 'You're playing with fire here,' Robertson said. 'That means that Whoop is taking a real calculated gamble.' Wearable technology sits in a grey area when it comes to regulation. The wearables market, estimated by one market intelligence group to be worth $84 billion in 2024, is rapidly expanding, and companies are racing to add new features that give users unique health measurements. Related : Smart wristbands, watches and rings that assess heart rates don't have to get cleared as medical devices. But Whoop competitors, such as Apple and Fitbit, have sought FDA approval for certain software tools in recent years. The crux of Whoop's argument rests on the 21st Century Cures Act, a 2016 law that exempts wellness software features from the definition of a medical device, so long as those features aren't related to the diagnosis, prevention, or treatment of a disease. Blood Pressure Insights, Whoop said, is only intended to be used as a way to gauge a person's performance, quality of sleep, and stress levels . The FDA, however, has rejected Whoop's characterization of the blood pressure tool. In its letter, the agency said the product qualifies as a medical device because its measurements are 'inherently associated with the diagnosis of a disease or condition,' such as hypertension, or high blood pressure. Advertisement Whoop has registered one of its products with the FDA, securing medical device approval for its Heart Screener tool. That tool measures the heart's electrical activity to alert users to potentially abnormal heart rates and atrial fibrillation, a common type of abnormal heart rhythm. The FDA said it doesn't comment on 'ongoing investigations, compliance matters or enforcement activities except with the company involved.' Related : The confrontation is reminiscent of the clash more than a decade ago between the FDA and the personal genomics platform 23andMe, said health law expert Frances Miller, who also teaches at Boston University. The FDA and 23andMe went back and forth on whether the company's health test — which the company claimed could tell customers their risk of conditions like gallstones, heart disease, or arthritis — constituted a medical device. In 2013, the FDA sent a warning letter to 23andMe much like the one it sent Whoop, and 23andMe ultimately capitulated. But the landscape looks different today, Miller said. The FDA has experienced significant cuts under President Trump, and federal agencies as a whole have lost power. In addition, Kennedy has publicly stated his vision that 'every American is wearing a wearable within four years.' Whether Whoop will win its fight against regulation is unclear, Miller said. 'I could have given you a very confident answer a year and a half ago,' Miller said. 'Not now. They're pushing the envelope.' Marin Wolf can be reached at

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