Anvisa expands indications for Wegovy and Ozempic to cardiovascular risks

Brazil's Anvisa approved on Monday, February 2, 2026, the expansion of therapeutic indications for semaglutide, the active ingredient in Wegovy and Ozempic. Wegovy can now be used to reduce the risk of heart attacks and strokes in adults with cardiovascular disease and overweight, while Ozempic is indicated for type 2 diabetes associated with chronic kidney disease. The agency is also reviewing a request for an oral version of Wegovy.

Brazil's National Health Surveillance Agency (Anvisa) announced on February 2, 2026, the expansion of indications for semaglutide, the active ingredient in Wegovy and Ozempic, produced by Novo Nordisk. Previously limited to obesity treatment, Wegovy is now authorized to reduce the risk of major cardiovascular events, such as heart attacks and strokes (AVC), in adults with established cardiovascular disease and obesity or overweight. This decision is based on studies showing significant reductions in these events when the drug is combined with a low-calorie diet and increased physical activity. In Brazil, around 400,000 deaths per year are caused by heart attacks or strokes.

For Ozempic, the approval extends its use to treating type 2 diabetes mellitus associated with chronic kidney disease. Data from the Brazilian Society of Nephrology in 2024 show that 29% of dialysis patients in the country are diabetic. The study presented by the manufacturer demonstrates that the drug, along with standard therapy, slows the progression of kidney failure and reduces deaths from major adverse cardiovascular events.

Cardiologist Silvio Giopato from the University of Campinas Clinical Hospital highlighted the potential for long-term reduction in heart attack incidence but warned about the high cost of the medications, ranging from R$ 825 to R$ 1,799 depending on dosage, and their unavailability in the public health system (SUS). "It's important to remember that although positive signals start in two to three years, full benefits only occur with continuous use of the medication. Clearly, the economic aspect weighs heavily, making the therapy inaccessible to most of the population," Giopato said.

Additionally, Novo Nordisk filed on January 30 for registration of an oral version of Wegovy, in 25 mg semaglutide tablets. If approved, it would be the first oral GLP-1 agonist for weight management. Clinical studies indicate an average weight loss of 16.6% of body weight, similar to the injectable version, with one-third of participants losing 20% or more. Rybelsus, another semaglutide-based product, is already sold in Brazil but only for type 2 diabetes.

संबंधित लेख

Illustration of oral semaglutide pill bottle with medical items symbolizing weight loss results from obesity trial.
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Oral semaglutide pill yields up to 16.6% weight loss in NEJM obesity trial

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A once-daily 25 mg oral form of semaglutide produced substantial weight loss in adults with obesity in a phase 3 study published in The New England Journal of Medicine, with a 16.6% mean reduction under an adherence-based analysis and 13.6% in the overall analysis. The results were accompanied by improvements in cardiometabolic risk factors and self-reported physical function. Novo Nordisk has submitted the therapy for U.S. approval and says U.S. manufacturing is underway; the FDA is slated to decide in the fourth quarter of 2025.

A prespecified analysis of the SELECT trial reports that weekly semaglutide lowered the risk of heart attacks and strokes by about 20% in adults with established cardiovascular disease and overweight or obesity—even when little weight was lost—suggesting benefits beyond slimming alone.

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Researchers led by Mass General Brigham and the Technical University of Munich report that tirzepatide and semaglutide are associated with significant reductions in heart attacks, strokes and death among adults with type 2 diabetes at elevated cardiovascular risk. Drawing on nearly one million insurance records, the Nature Medicine analysis finds strong and early heart protection from both GLP‑1–based drugs, with only modest differences between them.

UK specialists say strict early access rules for the weight-loss drug tirzepatide (Mounjaro) risk creating a “two-tier” obesity treatment system, with people who can pay privately getting faster access than those relying on the National Health Service.

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Alzheimer's trials are shifting to a multi-target approach inspired by cancer research, even after failures with Novo Nordisk's semaglutide. Only two drugs, Eli Lilly's Kisunla and Eisai and Biogen's Leqembi, are widely approved to slow progression. This evolution treats the brain-wasting disease as a complex system, seeking new ways to halt it amid its global impact.

दिल्ली हाई कोर्ट ने 12 जनवरी को एक फैसले में जायडस लाइफसाइंसेज को वैश्विक दवा कंपनी ब्रिस्टल मायर्स-स्क्विब के कैंसर ड्रग नivolumab का बायोसिमिलर वर्जन बनाने और बेचने की अनुमति दी है। यह फैसला भारत में कैंसर मरीजों के लिए सस्ती इम्यूनोथेरेपी उपचारों का रास्ता खोल सकता है। नivolumab कई प्रकार के कैंसर के खिलाफ प्रभावी है और इसका पेटेंट मई 2026 में समाप्त हो रहा है।

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अमेरिकी खाद्य एवं औषधि प्रशासन (एफडीए) ने थैलेसीमिया वाले वयस्कों में एनीमिया के इलाज के लिए मितापिवाट (एक्वेस्मे ब्रांड नाम से) को मंजूरी दे दी है, जो लाल रक्त कोशिकाओं की ऊर्जा सुधारकर काम करता है। यह गोली नियमित रक्त आधान की आवश्यकता वाले और न वाले दोनों रोगियों के लिए ली जा सकती है। विशेषज्ञों का कहना है कि यह भारत जैसे देशों में रोग प्रबंधन को बदल सकता है जहां थैलेसीमिया का बोझ अधिक है।

 

 

 

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