Health
Weight-loss experts predict 5 major treatment changes likely to emerge in 2026
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Big moves are continuing in the weight loss landscape in the new year following breakthrough research of GLP-1 medications and other methods.
Weight-loss experts spoke with Fox News Digital about their predictions for the most major changes to come in 2026.
No. 1: Shift to whole-body treatment
Dr. Peter Balazs, a hormone and weight loss specialist in New York and New Jersey, shared that the most important shift is likely to label GLP-1 drugs as “multi-system metabolic modulators” rather than “simple weight loss drugs.”
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“The treatment goal is no longer just BMI reduction, but total cardiometabolic risk mitigation, with effects now documented across the liver, heart, kidneys and vasculature,” he said.
“We are seeing a significant reduction in major adverse cardiovascular events … and progression of renal disease,” he went on.
The focus of GLP-1 drugs will widen beyond weight loss and diabetes, according to experts’ predictions. (iStock)
Philip Rabito, M.D., a specialist in endocrinology, weight loss and wellness in New York City, also shared that “exciting” advancements lie ahead for weight-loss drugs, including GLP-1s and GIPs.
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“These next‑generation agents, along with novel combinations that include glucagon and amylin agonists, are demonstrating even more impressive weight‑loss outcomes than currently available therapies, with the potential for better tolerability and sustained results,” he told Fox News Digital.
“There is also tremendous optimism around new federal agreements with manufacturers that aim to make these medications more widely accessible and affordable for the broad population of patients who need them most.”
No. 2: More convenient dosing
The typical prescription for a GLP-1 medication is a weekly injection, but delivery and dosing may be changing to more convenient methods in 2026, according to Balazs.
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A daily 25 mg pill version of Novo Nordisk’s Wegovy, a semaglutide designed to treat obesity, is now approved and available for chronic weight management, offering a non-injectable option for some patients.
A once-weekly oral GLP-1 is currently in phase 2 trials, as well as an implant that aims for three to six months of drug delivery, Balazs noted.
Incisionless weight-loss procedures will rise as a lower-risk option, according to experts. (iStock)
No. 3: Less invasive surgery
In addition to decreased risk during surgery for GLP-1 users, Balazs also predicted that metabolic surgery without incision will rise as a better option.
“Incisionless endoscopic procedures — like endoscopic sleeve gastroplasty (non-surgical weight-loss procedure that makes the stomach smaller from the inside) and duodenal mucosal resurfacing (non-surgical procedure that resets part of the small intestine to help the body better handle blood sugar) — [may become] more durable and widely available,” he said.
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“These offer significant metabolic benefits with shorter recovery and lower risk than traditional surgery.”
Rabito agreed that “rapid progress” in minimally invasive weight‑loss procedures is “opening powerful new options for patients who are hesitant to pursue traditional bariatric surgery.”
Bariatric surgery remains the most effective weight loss method, one specialist says. (iStock)
This avenue offers “meaningful and durable weight reduction with less risk, shorter recovery times and no external incisions,” the expert added.
Dr. Muhammad Ghanem, bariatric surgeon at the Orlando Health Weight Loss & Bariatric Surgery Institute, reiterated that surgery remains “the most successful modality for the treatment of obesity … with the highest weight loss and most durable outcomes as of yet.”
No. 4: Younger GLP-1 users
As Novo Nordisk’s Wegovy has been indicated for adolescents over 12 years old as an obesity treatment, Balazs commented that pediatric use of weight-loss drugs is “now a clinical reality.”
He predicted that other alternatives are likely to be approved in 2026 for younger users.
No. 5: High-tech, personalized access
Amid the growth of artificial intelligence, Balazs predicted an expansion in the clinical implementation of AI-driven weight-loss methods.
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This could include categorizing obesity into sub-types like “hungry brain,” “emotional hunger” and “slow burn” to personalize how therapy is prescribed while moving away from “trial and error,” he said.
Ghanem agreed that there will likely be a “big focus” on individualized testing for causes of obesity in 2026, as it’s a disease that can have “different causes in different people,” thus requiring different treatments.
AI and other digital opportunities will drive more access for weight-loss patients, experts say. (iStock)
The doctor anticipates that more patients will seek combinations of comprehensive treatments and programs.
“Patients are more aware that now we have a few weapons in our arsenal to combat obesity, and [they] are seeking a multidisciplinary and holistic approach,” Ghanem said.
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Treatment options will also turn digital with the rise of prescription digital therapeutics (PDTs) for weight loss, Balazs predicted.
“These are software applications delivering cognitive behavioral therapy, personalized nutrition and metabolic coaching through algorithms, often integrated with continuous glucose monitors, and reimbursed as medical treatments,” he said.
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Ghanem added that body composition analyzers, like DEXA scans, will likely be more widely used as awareness grows about the limitations of BMI and weight in assessing obesity.
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Health
Pancreatic cancer patient Ben Sasse sees ‘massive’ tumor reduction with experimental new drug
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Months after revealing his stage 4 cancer diagnosis, former U.S. Sen. Ben Sasse is speaking out about an experimental therapy that could extend his life.
Sasse, a Republican who represented Nebraska between 2015 and 2023, shared in December 2025 that he has metastatic pancreatic cancer, which has spread to multiple organs — including his liver and lungs.
After initially being given three to four months to live, Sasse, 54, entered a clinical trial for a drug called daraxonrasib, an oral therapy (pill) that is designed to block the defective gene that triggers uncontrolled cellular growth.
CANCER SURVIVAL APPEARS TO DOUBLE WITH COMMON VACCINE, RESEARCHERS SAY
The California-based drugmaker, Revolution Medicines, recently shared data from a phase 3 clinical trial of people with metastatic pancreatic cancer who did not respond to standard chemotherapy.
Patients on the treatment lived a median of 13 months, compared to around six months for those who continued with chemo.
Former Sen. Ben Sasse of Nebraska entered a clinical trial for a drug called daraxonrasib, an oral therapy (pill) that is designed to block the defective gene that triggers uncontrolled cellular growth. (Anna Moneymaker/Getty Images)
“I have much, much less pain than I had four months ago when I was diagnosed, and I have a massive 76% reduction in tumor volume over the last four months,” Sasse told “60 Minutes” in a recent interview.
Daraxonrasib works by going after a key growth “switch” in many cancers called RAS, according to Sarbajit Mukherjee, M.D., chief of gastrointestinal medical oncology at Miami Cancer Institute, part of Baptist Health South Florida.
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“In pancreatic cancer, that switch is stuck in the ‘on’ position in the vast majority of tumors, constantly telling the cancer cells to grow and spread,” the doctor, who was not involved in the trial and did not treat Sasse, told Fox News Digital.
“Daraxonrasib is designed to bind to RAS in its active state and turn down that signal, which can slow or shrink the cancer.”
“The drug is in the final stages of clinical trials, where it has been shown to double the survival of those previously treated for metastatic pancreatic cancer.”
Pancreatic cancer is difficult to diagnose early because there are generally no symptoms — or only subtle gastrointestinal symptoms — until it is already widespread, according to Dr. Marc Siegel, Fox News senior medical analyst.
“This is the first-of-its-kind targeted therapy for pancreatic cancer,” Siegel, who also was not involved in the research or the senator’s treatment, told Fox News Digital. “The drug is in the final stages of clinical trials, where it has been shown to double the survival of those previously treated for metastatic pancreatic cancer.”
Sasse, shown above, announced his diagnosis late last year. An expert noted that the survival boost seen from the clinical trial is a “big difference” for a disease that typically has much shorter survival times. (Win McNamee/Getty Images)
Mukherjee noted that the survival boost seen in the trial is a “big difference” for a disease that typically has much shorter survival times.
“From my perspective, as someone who treats pancreatic cancer every day, daraxonrasib is the first targeted pill in this disease that truly feels like a step change rather than a small incremental improvement,” he said.
“It opens the door to much more personalized strategies going forward. For a cancer where progress has been painfully slow, it could reshape how we care for patients with advanced disease.”
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While current chemotherapy options can shrink pancreatic tumors and help people live longer, they are “tough,” Mukherjee noted — “and once they stop working, our options are limited and survival is usually measured in just a few more months.”
Early data also suggest that when daraxonrasib is combined with standard chemotherapy as the first treatment, there is more shrinkage of tumors and more patients doing well at six months than they typically would only with chemotherapy.
Sasse shared in December 2025 that he has metastatic pancreatic cancer, which has spread to multiple organs, including his liver and lungs. (Meghan McCarthy/Palm Beach Daily News/USA TODAY NETWORK via Imagn Images)
If the drug is approved, it will likely become an important option for patients when standard chemotherapy stops working, Mukherjee suggested.
“Ongoing trials are now asking whether it should also be used as part of the very first treatment plan,” he added.
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Although the drug is described as “well-tolerated” compared to chemotherapy, the doctor noted that, like any strong cancer drug, daraxonrasib has side effects.
“The ones we see most often include rash, diarrhea, mouth sores and fatigue, with patients needing regular blood tests and close follow‑up while on treatment,” Mukherjee said.
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In the clinical trials, most of these problems have been managed by adjusting the dose or adding supportive medications.
“The limitations are important to be transparent about — it is still not yet FDA‑approved, and it is not a cure,” Mukherjee noted.
In addition to the daraxonrasi, Sasse credits his faith for helping him beat his original prognosis. (Drew Angerer/Getty Images)
“Over time, most cancers will eventually find ways to grow around the drug.”
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In addition to daraxonrasib, which he calls a “miracle” drug, Sasse credits his faith for helping him beat his original prognosis.
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“It’s weird to be in your early 50s and get a terminal diagnosis, and people all of a sudden act like you’re 93 or 94, and you have a lot of wisdom,” he said.
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“I don’t know that I have a lot of wisdom, but I have a lot of things that I think we should be reflecting on together.”
Fox News Digital reached out to Sasse for further comment, and to the head of the clinical trial as well.
The Supreme Court appeared divided on Monday during arguments in a dispute that could determine the fate of thousands of lawsuits that claim a widely used weedkiller causes cancer.
The case is the latest turn in a yearslong legal battle over safety concerns with the weedkiller Roundup. Developed by Monsanto in the 1970s, the herbicide is the focus of the lawsuits, which allege that it causes non-Hodgkin lymphoma.
The dispute before the justices stems from a 2019 lawsuit brought by a Missouri gardener, John Durnell, who used Roundup for years. Mr. Durnell claimed in his suit, filed in state court, that glyphosate, a chemical in the weedkiller, caused him to develop cancer.
During Monday’s oral argument, several of the justices expressed skepticism of arguments by Bayer, the German conglomerate that acquired Monsanto in 2018, and the Trump administration, which joined the case in support of the company, that federal rules requiring herbicide safety labeling should bar people from filing state-level claims that accuse companies of failing to warn consumers of dangers.
Chief Justice John G. Roberts Jr. asked a lawyer for the Trump administration whether states would be blocked from taking action if new scientific information raised alarms about a product.
“The states cannot do anything?” the chief justice asked.
Sarah M. Harris, a principal deputy solicitor general, responded that it would be problematic to have each state “jumping the gun” to come to its own conclusion about whether a product caused cancer.
Mr. Durnell’s lawyer argued that the federal Environmental Protection Agency had overreached its regulatory power, a problem that could be rectified by giving a role to the courts, including at the state level. Several of the justices appeared skeptical about that argument too, questioning whether such a ruling would lead to a patchwork of safety regulations throughout the country.
In 2023, a Missouri jury awarded Mr. Durnell $1.25 million in damages. If the court finds for the company, that verdict would be erased and other claims against the company also endangered. If the court finds for Mr. Durnell, not only would his verdict be upheld but it would also clear the way for a flood of other lawsuits to proceed in courts throughout the country.
A ruling is expected by the end of June or early July.
The central issue in the case involves a collision between state and federal power. Bayer has argued that Mr. Durnell’s victory in Missouri is barred by a federal law, the Federal Insecticide, Fungicide and Rodenticide Act. That statute requires herbicides to be registered with the E.P.A. before they can be sold. Companies must submit scientific and safety data to the agency, along with proposed label information, including safety warnings.
The E.P.A. has previously determined that Roundup is safe to use. Bayer argued that the Missouri court ruling conflicted with that federal determination. Paul D. Clement, who represented Bayer, asserted that the federal agency’s decision invalidates the state court decision.
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Bayer has also said it cannot add warnings to Roundup in any state because they would contradict the E.P.A.’s findings.
In a brief to the justices, lawyers for Bayer wrote that the E.P.A. had “repeatedly determined” that glyphosate does not cause cancer, asserting that the company would not be able to “unilaterally alter the label’s precautionary warnings to include a cancer warning.”
The company appealed the jury verdict in the Missouri case and, after the Missouri Court of Appeals upheld the trial court, asked the justices to weigh in.
Early this year, President Trump issued an executive order that cited the Defense Production Act to guarantee production of glyphosate-based herbicides, appearing to elevate Roundup to a national security priority.
Lawyers for Mr. Durnell argued that nothing in the federal law blocked Bayer from adding a cancer warning to its labels and that such a change would not require E.P.A. approval.
Mr. Durnell was represented by Ashley C. Keller and Jonathan F. Mitchell, a prominent conservative appellate lawyer who represented Mr. Trump in his successful 2024 bid to remain on the Colorado ballot. Both lawyers joined the Supreme Court case only in recent months.
Another lawyer, David C. Frederick, had initially filed briefs on Mr. Durnell’s behalf. In the weeks before the argument, Mr. Frederick asked the justices if he could participate in the argument on behalf of more than 11,500 other people whose claims would be affected by the court’s decision. The justices denied the request.
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