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RFK Jr's new vaccine panel opens with scandal after citing non-existent study

RFK Jr's new vaccine panel opens with scandal after citing non-existent study

News2425-06-2025
RFK Jr dismissed all 17 members of the Advisory Committee on Immunisation Practices (ACIP) and appointed eight new members.
The panel's first meeting opened under controversy when a planned presentation cited a completely non-existent 2008 study.
The new panel plans to revisit long-settled vaccine science.
A medical panel appointed by US Health Secretary Robert F Kennedy Jr opened its first meeting on Wednesday under a cloud of controversy after a presentation it planned to review cited a non-existent study.
The Advisory Committee on Immunisation Practices (ACIP), an independent body that reviews scientific evidence to recommend which groups should receive vaccines and when, rarely makes headlines.
But its work has come under fresh scrutiny after Kennedy - who spent two decades spreading vaccine misinformation before becoming President Donald Trump's top health official - abruptly dismissed all 17 sitting ACIP members earlier this month, accusing them of pharmaceutical industry conflicts of interest.
He then appointed eight new members, including scientist Robert Malone, widely known for spreading false claims during the Covid-19 pandemic, and Martin Kulldorff, chair of the panel and a co-signatory of the Great Barrington Declaration, which called for an end to lockdowns in October 2020 - months before Covid vaccines became available.
The posted agenda signalled the panel would revisit long-settled debates around thimerosal, a vaccine preservative, and highlight rare side-effects linked to measles shots, with no planned discussion of their enormous public health benefits.
READ | US Senate votes in Trump's controversial pick Robert F Kennedy Jr as secretary of health
Lyn Redwood, a nurse and former leader of Children's Health Defence - an anti-vaccine group once chaired by RFK Jr - is set to present on thimerosal.
Scientists reviewing her slides found she had cited a non-existent 2008 study by RF Berman titled "Low-level neonatal thimerosal exposure: Long-term consequences in the brain." In fact, no such study exists.
While Berman did publish a paper that year, it appeared in a different journal and found no evidence linking thimerosal to autism.
The presentation was quietly removed and replaced without explanation.
Revisiting established science
Opening the meeting, Kulldorff lamented his firing by Harvard University for refusing the Covid vaccine.
He also announced the formation of a new working group to re-examine the wisdom of Hepatitis B shots for babies "at the day of birth."
Experts met the announcement with scepticism.
"The rationale for Hepatitis B vaccination prior to hospital discharge (not day or birth) for neonates is well documented and established - but it's another pet cause of the anti-vaccine movement so not surprising it's being mentioned," Amesh Adalja, an infectious disease expert at Johns Hopkins University told AFP.
Similarly, thimerosal is a mercury-based preservative long used in medicines, with no evidence of harm at low doses.
"Study after study showed that the ethylmercury in those vaccines never contributed in any important way to the burden of mercury that one is exposed to, living on this planet," vaccine expert Paul Offit of the Children's Hospital of Philadelphia told AFP.
Still, vaccine makers agreed to remove it from paediatric vaccines in 1999 in response to public concern. It remains in some flu shots.
Measles running rampant
For childhood immunisations, US parents can opt for a combined measles, mumps, rubella, and varicella (MMRV) shot or two separate injections - one for MMR and the other for varicella.
The combination spares children an extra jab but carries a slightly higher risk of febrile seizures, a rare and typically harmless side-effect.
Separating the shots is already recommended for the first dose at 12-47 months, leaving experts puzzled as to why the issue is being revisited.
"This working group may also look at new research concerning the optimal timing of the
measles, mumps and rubella (MMR) vaccine to resolve religious objections that some parents have concerning the MMR vaccine being used here in the United States," said Kulldorff.
The US, which declared measles eliminated in 2000, is currently experiencing its worst outbreak in decades, with more than 1 200 cases and three confirmed deaths.
The panel's recommendations could have broad consequences, shaping school vaccine mandates and insurance coverage.
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Implantable Device Shows Promise for Preventing Hypoglycemia
Implantable Device Shows Promise for Preventing Hypoglycemia

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Implantable Device Shows Promise for Preventing Hypoglycemia

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Former K-9 Maple is busy as a bee sniffing out threats to Michigan State University colonies
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Former K-9 Maple is busy as a bee sniffing out threats to Michigan State University colonies

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Belite Bio Reports Second Quarter 2025 Financial Results and Provides a Corporate Update
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Associated Press

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Belite Bio Reports Second Quarter 2025 Financial Results and Provides a Corporate Update

SAN DIEGO, Aug. 11, 2025 (GLOBE NEWSWIRE) -- Belite Bio, Inc (NASDAQ: BLTE), a clinical-stage drug development company focused on advancing novel therapeutics targeting degenerative retinal diseases that have significant unmet medical needs, today announced its financial results for the second quarter ended June 30, 2025, and provided a general business update. 'This quarter, we remained on track with the strategic objectives we outlined at the start of the year, including the completion of enrollment in our pivotal Phase 3 PHOENIX trial — an important milestone in our development efforts for people living with geographic atrophy,' said Dr. Tom Lin, Chairman and CEO of Belite Bio. 'We also received Breakthrough Therapy Designation for Tinlarebant for the treatment of Stargardt disease from the FDA, underscoring its potential as the first-ever treatment for this patient population and acknowledging the significant unmet need for people living with this debilitating disease. 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For the six months ended June 30, 2025, general and administration expenses were $12.7 million compared to $3.0 million for the same period in 2024. The increase in general and administrative expenses in both the quarter and year-to-date was primarily due to an increase in share-based compensation expenses. Other Income: For the three months ended June 30, 2025, other income was $1.3 million compared to $1.0 million for the same period in 2024. For the six months ended June 30, 2025, other income was $2.5 million compared to $1.4 million for the same period in 2024. The increase in both the quarter and year-to-date was attributed to interest from time deposits and U.S. treasury bills. Net Loss: For the three months ended June 30, 2025, the Company reported a net loss of $16.3 million, compared to a net loss of $9.5 million for the same period in 2024. For the six months ended June 30, 2025, the Company reported a net loss of $30.6 million, compared to a net loss of $17.4 million for the same period in 2024. Webcast Information Belite Bio will host a webcast on Monday, August 11, 2025, at 4:30 p.m. Eastern Time to discuss the Company's financial results and provide a business update. To join the webcast, please visit A replay will be available for approximately 90 days following the event. About Belite Bio Belite Bio is a clinical-stage drug development company focused on advancing novel therapeutics targeting degenerative retinal diseases that have significant unmet medical need, such as Stargardt disease type 1 (STGD1) and Geographic Atrophy (GA) in advanced dry age-related macular degeneration (AMD), in addition to specific metabolic diseases. Belite's lead candidate, Tinlarebant, an oral therapy intended to reduce the accumulation of toxins in the eye, is currently being evaluated in a Phase 3 study (DRAGON) and a Phase 2/3 study (DRAGON II) in adolescent STGD1 subjects and a Phase 3 study (PHOENIX) in subjects with GA. For more information, follow us on X, Instagram, LinkedIn, and Facebook or visit us at Important Cautions Regarding Forward Looking Statements This press release contains forward-looking statements about future expectations and plans, as well as other statements regarding matters that are not historical facts. These statements include but are not limited to statements regarding the potential implications of clinical data for patients, and Belite Bio's advancement of, and anticipated preclinical activities, clinical development, regulatory milestones, and commercialization of its product candidates, and any other statements containing the words 'expect', 'hope' and similar expressions. Actual results may differ materially from those indicated in the forward-looking statements as a result of various important factors, including but not limited to Belite Bio's ability to demonstrate the safety and efficacy of its drug candidates; the clinical results for its drug candidates, which may not support further development or regulatory approval; the timing to complete relevant clinical trials and/or to receive the interim/final data of such clinical trials; the timing to submit trial data to regulatory authorities for drug approval; the content and timing of decisions made by the relevant regulatory authorities regarding regulatory approval of Belite Bio's drug candidates; the potential efficacy of Tinlarebant, as well as those risks more fully discussed in the 'Risk Factors' section in Belite Bio's filings with the U.S. Securities and Exchange Commission. All forward-looking statements are based on information currently available to Belite Bio, and Belite Bio undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required by law. Media and Investor Relations Contact: Jennifer Wu [email protected] Julie Fallon [email protected]

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