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Congressional committees push back on Trump's proposed NOAA budget cuts

Congressional committees push back on Trump's proposed NOAA budget cuts

Yahoo23-07-2025
Lawmakers from both parties have so far rejected steep cuts to the National Oceanic and Atmospheric Administration (NOAA) proposed by the Trump administration and reiterated their support for a fully staffed National Weather Service (NWS) during recent committee meetings, which included key appropriations markup sessions.
While the House and Senate spending bills for fiscal year 2026 are still in the early stages of the legislative process, initial drafts indicate bipartisan pushback against the significant cuts outlined in the administration's budget proposal, released earlier this year.
For fiscal year 2026, which begins Oct. 1, the Trump administration proposed cutting NOAA's budget by roughly 25%, including the elimination of its research division, the Office of Oceanic and Atmospheric Research (OAR) and making major reductions to other key offices such as the National Centers for Environmental Information (NCEI), the world's largest provider of weather and climate data.
MORE: After Texas flood, elected leaders say cuts to FEMA, NOAA could affect weather response
The budget proposal stated, "The FY 2026 budget eliminates all funding for climate, weather, and ocean Laboratories and Cooperative Institutes. It also does not fund Regional Climate Data and Information, Climate Competitive Research, the National Sea Grant College Program, Sea Grant Aquaculture Research, or the National Oceanographic Partnership Program."
The House Appropriations Subcommittee on Commerce, Justice, Science and Related Agencies advanced a spending bill with bipartisan support last week that would fund NOAA at levels mostly in line with budgets of previous years.
The fiscal year 2026 Commerce, Justice, Science appropriations bill provides roughly $5.8 billion to NOAA in 2026, a 6% decrease from the previous year. However, it restores a majority of funding for NOAA's Operations, Research and Facilities (ORF) account, which includes OAR. While specific spending details have not yet been released, this would likely spare many critical research labs and climate institutes from potential cuts.
During the July 15 markup session, Subcommittee Chairman Hal Rogers, R-Ky., expressed his support for the National Weather Service, emphasizing the recent toll of devastating flooding hitting the country.
"Flooding has inflicted much pain on this nation over the last few months," he said. "From my district in Kentucky to Texas, now is the time to ensure the National Weather Service is equipped with the funding it needs to warn and protect our citizens."
MORE: Senate considers Neil Jacobs, 'Sharpiegate' scientist, as NOAA administrator
At the start of the markup session, Rosa DeLauro, D-Conn., the subcommittee's ranking Democrat, voiced concerns over both the proposed NOAA budget and recent staffing and funding cuts at the National Weather Service.
"Weather forecasts are not waste, fraud and abuse," she said. "I ask my colleagues, did anyone come to your town halls and complain that the National Weather Service has too many meteorologists? Too many people issuing advisories, watches and warnings on severe storms?"
DeLauro also cited concerns from Bill Turner, Connecticut's state emergency management director, who said the situation is "a very fragile house of cards right now, and we need them to continue… It really could be catastrophic in a lot of ways for our state if they go down that path of stopping the National Weather Service and their functionality."
The bill now advances to the full committee for a markup on Thursday, July 24.
The Senate's version of the bill allocates approximately $6.14 billion to NOAA for fiscal year 2026, just below the $6.18 billion approved for 2025. While this represents a modest overall decrease, the Senate Committee on Appropriations voted to boost spending for the agency's Operations, Research and Facilities (ORF) account, adding $68.7 million. The increase means more available funding that could go to key offices such as OAR, NWS and NESDIS (National Environmental Satellite, Data, and Information Service).
MORE: Hurricane season is here and meteorologists are losing a vital tool for forecasting them
The current Senate bill explicitly signals support for NOAA's mission, including weather and climate research.
"The Committee strongly supports Climate Laboratories and Cooperative Institutes for their critical role in delivering high-quality weather information and driving economic benefits across the United States," the bill states.
The bill also addresses staffing concerns at local NWS offices across the country and provides additional funding to ensure they become fully staffed.
The bill's authors write, "Insufficient staffing levels risk compromising public safety and the NWS's mission to protect lives and property. The Committee provides an additional $10,000,000 for Analyze, Forecast and Support and urges the NWS to prioritize recruitment, retention, and training initiatives to ensure all weather forecast offices (WFOs) are fully staffed."
While introducing the bill, Jerry Moran, R- Kan., chairman of the Senate Appropriations Subcommittee on Commerce, Science and Justice, said, "NOAA, and particularly the National Weather Service, is a hugely important component of what this bill funds, and this bill recognizes that importance." He added that the bill "fully funds the National Weather Service" and "eliminates any reduction in the workforce."
However, Brian Schatz, D-Hawaii, raised concerns that the bill still gave too much discretion to the Office of Management and Budget (OMB) to determine the staffing levels needed to fulfill the agency's mission and statutory obligation -- "the Office of Management and Budget which clearly made the judgment that the National Weather Service has too many human beings working," Schatz said.
He introduced an amendment that would have required the administration to maintain full-time staffing at levels in place as of Sept. 30, 2024, but it was rejected along party lines.
The Senate Committee on Appropriations approved the Fiscal Year 2026 Commerce, Justice, Science, and Related Agencies Appropriations Act on July 17 by a vote of 19-10.
MORE: How job cuts at NOAA could impact weather forecasting
What does the Trump Administration want to cut?
The administration's budget proposal calls for eliminating the Office of Oceanic and Atmospheric Research (OAR) as a NOAA Line Office, with several of its functions transferred to the National Weather Service and the National Ocean Service. OAR leads NOAA's weather and climate research and develops many of the forecasting tools meteorologists rely on to produce timely and accurate forecasts.
The proposed budget would include shutting down NOAA's nationwide network of research labs and cooperative institutes. Among them is the Global Systems Laboratory in Boulder, Colorado, where the High-Resolution Rapid Refresh (HRRR) model, a critical tool in modern weather forecasting, was first developed more than a decade ago. The HRRR model helps meteorologists track everything from severe thunderstorms to extreme rainfall to wildfire smoke.
The Global Monitoring Laboratory, also based in Boulder, oversees operations at Mauna Loa Observatory on Hawaii's Big Island. This observatory has maintained the world's longest continuous observation of atmospheric carbon dioxide and has been crucial to our understanding of how human-caused greenhouse gas emissions fuel global warming.
NOAA's Atlantic Oceanographic and Meteorological Laboratory (AOML) in Miami, Florida, plays a vital role in operational hurricane forecasting. The lab develops cutting-edge tropical weather models that have significantly improved forecast accuracy in recent decades. National Hurricane Center (NHC) forecasters set a record for forecast track accuracy in 2024, according to a NOAA report. NHC issued 347 official forecasts during the 2024 Atlantic hurricane season, and its track predictions set accuracy records at every forecast time period.
MORE: DOGE now has access to NOAA's IT systems; reviewing DEI program, sources say
Who will lead NOAA next?
Earlier this month, during a confirmation hearing, Dr. Neil Jacobs, President Donald Trump's nominee to head NOAA, said he supports the administration's proposal to significantly cut the agency's budget arguing the reductions could be achieved by shifting work from research to operations without impacting "mission essential functions."
Jacobs also said if confirmed, he would "ensure that staffing the weather service offices is a top priority," adding that, "It's really important for the people to be there because they have relationships with the people in the local community. They're a trusted source."
NOAA's 2025 budget costs Americans less than $20 per person this year.
ABC News reached out to NOAA for comment, but did not immediately hear back.
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US lenders weighed reputation rules, not politics, in closing accounts, sources say
US lenders weighed reputation rules, not politics, in closing accounts, sources say

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US lenders weighed reputation rules, not politics, in closing accounts, sources say

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Lilly's oral GLP-1, orforglipron, delivers weight loss of up to an average of 27.3 lbs in first of two pivotal Phase 3 trials in adults with obesity
Lilly's oral GLP-1, orforglipron, delivers weight loss of up to an average of 27.3 lbs in first of two pivotal Phase 3 trials in adults with obesity

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Lilly's oral GLP-1, orforglipron, delivers weight loss of up to an average of 27.3 lbs in first of two pivotal Phase 3 trials in adults with obesity

In ATTAIN-1, the investigational once-daily oral pill showed significant efficacy, and a safety and tolerability profile consistent with injectable GLP-1 therapies at 72 weeks Orforglipron achieved the primary and all key secondary endpoints, including demonstrating improvements in a number of cardiovascular risk factors With these results, Lilly is on track to submit orforglipron to global regulatory agencies by year-end and is making substantial investments to meet anticipated demand at launch INDIANAPOLIS, Aug. 7, 2025 /PRNewswire/ -- Eli Lilly and Company (NYSE: LLY) today announced positive topline results from the Phase 3 ATTAIN-1 trial, evaluating orforglipron, an investigational oral glucagon-like peptide-1 (GLP-1) receptor agonist, in 3,127 adults with obesity, or overweight with a weight-related medical problem and without diabetes. At 72 weeks, all three doses of orforglipron, met the primary endpoint and all key secondary endpoints compared to placebo, delivering clinically meaningful weight loss as an adjunct to a healthy diet and physical activity. For the primary endpoint, orforglipron 36 mg, taken once per day without food and water restrictions, lowered weight by an average of 12.4% (27.3 lbs) compared to 0.9% (2.2 lbs) with placebo using the efficacy estimand.1 "Obesity is one of the most pressing global health challenges of our time, driving global chronic disease burden and impacting more than one billion people worldwide," said Kenneth Custer, Ph.D., executive vice president and president of Lilly Cardiometabolic Health. "With orforglipron, we're working to transform obesity care by introducing a potential once-daily oral therapy that could support early intervention and long-term disease management, while offering a convenient alternative to injectable treatments. With these positive data in hand, we are now planning to submit orforglipron for regulatory review by year-end and are prepared for a global launch to address this urgent public health need." In the ATTAIN-1 trial, orforglipron met the primary endpoint of superior body weight reduction compared to placebo. Participants taking the highest dose of orforglipron lost an average of 27.3 lbs (12.4%) at 72 weeks using the efficacy estimand. In a key secondary endpoint, 59.6% of participants taking the highest dose of orforglipron lost at least 10% of their body weight, while 39.6% lost at least 15% of their body weight. In addition to achieving significant weight loss, orforglipron was also associated with reductions in known markers of cardiovascular risk, including non-HDL cholesterol, triglycerides and systolic blood pressure in pooled analyses across all doses. In a pre-specified exploratory analysis, the highest dose of orforglipron reduced high-sensitivity C-reactive protein (hsCRP) levels by 47.7%. Efficacy Estimand ResultsOrforglipron 6 mg Orforglipron 12 mg Orforglipron 36 mg Placebo Primary Endpoint Mean percent change in body weight from of 103.2 kg(227.5 lbs) and 37.0 BMIi -7.8% (-8.0 kg; -17.6 lbs) -9.3% (-9.4 kg; -20.7 lbs) -12.4% (-12.4 kg; -27.3 lbs) -0.9% (-1.0 kg; -2.2 lbs) Key Secondary Endpoints Percentage of participants achievingbody weight reductionsof ≥10%i 35.9 % 45.1 % 59.6 % 8.6 % Percentage of participants achieving body weight reductionsof ≥15%i 16.5 % 24.0 % 39.6 % 3.6 % iSuperiority test was adjusted for multiplicity. For the treatment-regimen estimand,2 each dose of orforglipron led to statistically significant improvements across the primary and all key secondary endpoints. Percent weight reduction: -7.5% (-7.8 kg; 17.2 lbs; 6 mg), -8.4% (-8.6 kg; 19.0 lbs; 12 mg), -11.2% (-11.3 kg; 25.0 lbs; 36 mg), -2.1% (-2.4 kg; 5.3 lbs; placebo) Percentage of participants achieving body weight reductions of ≥10%: 33.3% (6 mg), 40.0% (12 mg), 54.6% (36 mg), 12.9% (placebo) Percentage of participants achieving body weight reductions of ≥15%: 15.1% (6 mg), 20.3% (12 mg), 36.0% (36 mg), 5.9% (placebo) The overall safety profile of orforglipron in ATTAIN-1 was consistent with the established GLP-1 receptor agonist class. The most commonly reported adverse events were gastrointestinal-related and generally mild-to-moderate in severity. The most common adverse events for participants treated with orforglipron (6 mg, 12 mg and 36 mg, respectively) were nausea (28.9%, 35.9% and 33.7%) vs. 10.4% with placebo, constipation (21.7%, 29.8% and 25.4%) vs. 9.3% with placebo, diarrhea (21.0%, 22.8% and 23.1%) vs. 9.6% with placebo, vomiting (13.0%, 21.4% and 24.0%) vs. 3.5% with placebo, and dyspepsia (13.0%, 16.2% and 14.1%) vs. 5.0% with placebo. Treatment discontinuation rates due to adverse events were 5.1% (6 mg), 7.7% (12 mg) and 10.3% (36 mg) for orforglipron vs. 2.6% with placebo. The overall treatment discontinuation rates were 21.9% (6 mg), 22.5% (12 mg) and 24.4% (36 mg) for orforglipron vs. 29.9% with placebo. No hepatic safety signal was observed. The detailed ATTAIN-1 results will be presented next month at the European Association for the Study of Diabetes (EASD) Annual Meeting 2025 and published in a peer-reviewed journal. More results from the ATTAIN Phase 3 clinical trial program will be shared later this year, along with findings from the ACHIEVE Phase 3 clinical trial program evaluating orforglipron for adults with type 2 diabetes. About orforglipron Orforglipron (or-for-GLIP-ron) is an investigational, once-daily small molecule (non-peptide) oral glucagon-like peptide-1 receptor agonist that can be taken any time of the day without restrictions on food and water intake.3 Orforglipron was discovered by Chugai Pharmaceutical Co., Ltd. and licensed by Lilly in 2018. Chugai and Lilly published the preclinical pharmacology data of this molecule together.4 Lilly is running Phase 3 studies on orforglipron for the treatment of type 2 diabetes and for weight management in adults with obesity or overweight with at least one weight-related medical problem. It is also being studied as a potential treatment for obstructive sleep apnea (OSA) and hypertension in adults with obesity. About ATTAIN-1 and ATTAIN clinical trial program ATTAIN-1 (NCT05869903) is a Phase 3, 72-week, randomized, double-blind, placebo-controlled trial comparing the efficacy and safety of orforglipron 6 mg, 12 mg and 36 mg as monotherapy to placebo in adults with obesity, or overweight with at least one of the following comorbidities: hypertension, dyslipidemia, OSA or cardiovascular disease, who did not have diabetes. The trial randomized 3,127 participants across the U.S., Brazil, China, India, Japan, South Korea, Puerto Rico, Slovakia, Spain and Taiwan in 3:3:3:4 ratio to receive either 6 mg, 12 mg or 36 mg orforglipron or placebo. The primary objective of the study was to demonstrate that orforglipron (6 mg, 12 mg, 36 mg) is superior to placebo in body weight reduction from baseline after 72 weeks in people with a BMI ≥30.0 kg/m² or a BMI ≥27.0 kg/m² with at least one weight-related comorbidity and a history of at least one self-reported unsuccessful dietary effort to lose body weight. All participants in the orforglipron treatment arms started the study at a dose of orforglipron 1 mg once-daily and then increased the dose in a step-wise approach at four-week intervals to their final randomized maintenance dose of 6 mg (via steps at 1 mg and 3 mg), 12 mg (via steps at 1 mg, 3 mg and 6 mg) or 36 mg (via steps at 1 mg, 3 mg, 6 mg, 12 mg and 24 mg). Dose reduction was only allowed for GI tolerability if other mitigations failed. The ATTAIN Phase 3 global clinical development program for orforglipron has enrolled more than 4,500 people with obesity or overweight across two global registration trials. The program began in 2023 with additional results anticipated this year. About LillyLilly is a medicine company turning science into healing to make life better for people around the world. We've been pioneering life-changing discoveries for nearly 150 years, and today our medicines help tens of millions of people across the globe. Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing new discoveries to solve some of the world's most significant health challenges: redefining diabetes care; treating obesity and curtailing its most devastating long-term effects; advancing the fight against Alzheimer's disease; providing solutions to some of the most debilitating immune system disorders; and transforming the most difficult-to-treat cancers into manageable diseases. With each step toward a healthier world, we're motivated by one thing: making life better for millions more people. That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable. To learn more, visit and or follow us on Facebook, Instagram and LinkedIn. P-LLY Endnotes and References: The efficacy estimand represents efficacy had all randomized participants remained on study intervention (with possible dose interruptions and modifications) for 72 weeks without initiating prohibited weight management treatments. The treatment-regimen estimand represents the estimated average treatment effect regardless of adherence to study intervention or initiation of prohibited weight management treatments. Ma X, Liu R, Pratt EJ, Benson CT, Bhattachar SN, Sloop KW. Effect of Food Consumption on the Pharmacokinetics, Safety, and Tolerability of Once-Daily Orally Administered Orforglipron (LY3502970), a Non-peptide GLP-1 Receptor Agonist. Diabetes Ther. 2024 Apr;15(4):819-832. doi: 10.1007/s13300-024-01554-1. Epub 2024 Feb 24. PMID: 38402332; PMCID: PMC10951152. T. Kawai, B. Sun, H. Yoshino, D. Feng, Y. Suzuki, M. Fukazawa, S. Nagao, D.B. Wainscott, A.D. Showalter, B.A. Droz, T.S. Kobilka, M.P. Coghlan, F.S. Willard, Y. Kawabe, B.K. Kobilka, & K.W. Sloop, Structural basis for GLP-1 receptor activation by LY3502970, an orally active nonpeptide agonist, Proc. Natl. Acad. Sci. U.S.A. 117 (47) 29959-29967, (2020). Cautionary Statement Regarding Forward-Looking Statements This press release contains forward-looking statements (as that term is defined in the Private Securities Litigation Reform Act of 1995) about orforglipron as a potential treatment for adults with obesity or overweight, Lilly's ability to supply orforglipron, if approved, and the timeline for future readouts, presentations, and other milestones relating to orforglipron and its clinical trials and reflects Lilly's current beliefs and expectations. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of drug research, development, and commercialization. Among other things, there is no guarantee that planned or ongoing studies will be completed as planned, that future study results will be consistent with study results to date, that orforglipron will prove to be a safe and effective treatment for obesity or overweight, that orforglipron will receive regulatory approval, or that Lilly will execute its strategy as expected. For further discussion of these and other risks and uncertainties that could cause actual results to differ from Lilly's expectations, see Lilly's Form 10-K and Form 10-Q filings with the United States Securities and Exchange Commission. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release. Trademarks and Trade NamesAll trademarks or trade names referred to in this press release are the property of the company, or, to the extent trademarks or trade names belonging to other companies are references in this press release, the property of their respective owners. Solely for convenience, the trademarks and trade names in this press release are referred to without the ® and ™ symbols, but such references should not be construed as any indicator that the company or, to the extent applicable, their respective owners will not assert, to the fullest extent under applicable law, the company's or their rights thereto. We do not intend the use or display of other companies' trademarks and trade names to imply a relationship with, or endorsement or sponsorship of us by, any other companies. Refer to: Brooke Frost; 317-432-9145 (Media)Michael Czapar; czapar_michael_c@ 317-617-0983 (Investors) View original content to download multimedia: SOURCE Eli Lilly and Company Sign in to access your portfolio

Breakthrough study finds deficiency of this common nutrient could contribute to Alzheimer's
Breakthrough study finds deficiency of this common nutrient could contribute to Alzheimer's

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Breakthrough study finds deficiency of this common nutrient could contribute to Alzheimer's

A deficiency of the metal lithium in the body could be a key factor contributing to the development of dementia in Alzherimer's patients, a groundbreaking new study reveals. The decade-long research, published in the journal Nature, shows for the first time that lithium occurs naturally in the brain and maintains the normal function of all its major cell types, preventing nerves from degradation. Scientists from Harvard Medical School found that lithium loss in the human brain is one of the earliest changes leading to Alzheimer's, while in mice, a similar lithium depletion accelerated memory decline. A reduced lithium level was found in some cases due to the metal's impaired uptake and its binding to amyloid plaques, which are known to be smoking gun signs of Alzheimer's. Researchers also showed that a new type of lithium compound – lithium orotate – can avoid capture by amyloid plaques and restore memory in mice. In the study, scientists used an advanced type of mass spectroscopy chemical analysis method to measure trace levels of about 30 different metals in the brain and blood samples from a range of people, including cognitively healthy people, those in an early stage of dementia, and those with advanced Alzheimer's. The analysis revealed that lithium was the only metal with markedly different levels across groups, which also seemed to change at the earliest stages of memory loss. 'Lithium turns out to be like other nutrients we get from the environment, such as iron and vitamin C,' study senior author Bruce Yankner said. 'It's the first time anyone's shown that lithium exists at a natural level that's biologically meaningful without giving it as a drug,' Dr Yankner said. Although lithium compounds have been historically in use to treat a range of mental conditions like bipolar disorder and major depressive disorder, in these cases, they are given at much higher concentrations that could even be toxic to older people. Scientists have now found that lithium orotate is effective at one-thousandth this dose – enough to mimic the natural level of lithium in the brain. The latest findings with lithium orotate, however, needs to be confirmed in humans via clinical trials. Yet, researchers suspect that measuring lithium levels could help screen people for early Alzheimer's. The findings revise the theory of Alzheimer's disease, which affects nearly 400 million people worldwide, offering a new strategy for early diagnosis, prevention, and treatment. Decades of studies have shown that Alzheimer's disease involves an array of brain abnormalities, including clumps of the protein amyloid beta, tangles of the protein tau, and a loss of the brain's protective protein REST. However, these abnormalities have never fully explained the condition. For instance, it remains unclear why some people with Alzheimer's-like changes in the brain never go on to develop dementia or cognitive decline. Recent treatments developed to target amyloid beta plaques also don't seem to reverse memory loss, only modestly reducing the rate of cognitive decline. Now, scientists say lithium could be the critical missing link. 'The idea that lithium deficiency could be a cause of Alzheimer's disease is new and suggests a different therapeutic approach,' Dr Yankner said. 'You have to be careful about extrapolating from mouse models, and you never know until you try it in a controlled human clinical trial... But so far the results are very encouraging,' he added. Solve the daily Crossword

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