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.

関連記事

Illustration of oral semaglutide pill bottle with medical items symbolizing weight loss results from obesity trial.
AIによって生成された画像

経口セマグルチド錠がNEJMの肥満試験で最大16.6%の体重減少をもたらす

AIによるレポート AIによって生成された画像 事実確認済み

1日1回の25mg経口セマグルチドは、The New England Journal of Medicineに掲載された第3相試験で、肥満の成人において大幅な体重減少を引き起こし、遵守ベースの分析で平均16.6%の減少、全体分析で13.6%の減少を示した。結果は、心代謝リスク要因と自己報告身体機能の改善を伴った。Novo Nordiskは米国承認を申請しており、米国製造が進行中と述べている;FDAは2025年第4四半期に決定を予定している。

SELECT試験の事前指定分析によると、週1回のセマグルチドは、心血管疾患が確立された過体重または肥満の成人において、心臓発作と脳卒中のリスクを約20%低減した—体重減少がわずかであっても—これは、痩せること以上の利点を示唆している。

AIによるレポート 事実確認済み

Mass General Brighamとミュンヘン工科大学主導の研究者らが、チルゼパチドとセマグルチドが、心血管リスクが高い2型糖尿病成人における心筋梗塞、脳卒中、死亡の有意な減少と関連していると報告。約100万件の保険記録を基にした*Nature Medicine*の分析では、両GLP-1系薬剤が強力かつ早期の心臓保護効果を示し、両者の差はわずかだった。

英国の専門家らは、体重減少薬tirzepatide(Mounjaro)の初期アクセス厳格ルールが「二層式」の肥満治療システムを生むリスクがあるとし、私的支払いが可能な人が国民保健サービス(NHS)に頼る人より速いアクセスを得ると述べている。

AIによるレポート

ノボノルディスクのセマグルチド試験の失敗にもかかわらず、アルツハイマー病治療の研究はがん治療のように複雑な経路を標的とするアプローチへ移行している。現在、進行を遅らせる承認された薬はエリ・リリーのキスンラとエーザイおよびバイオジェンのレカンビの2つだけだ。この変化は、世界中で数百万人の脳の消耗性疾患に取り組むための新たな標的と戦略の特定を目指す。

A Delhi High Court verdict on January 12 has allowed Indian pharma company Zydus Lifesciences to manufacture and sell a biosimilar version of Bristol Myers-Squibb's cancer drug Nivolumab. This ruling could pave the way for more affordable immunotherapy treatments for cancer patients in India. Nivolumab is effective against various cancers, with its patent set to expire in May 2026.

AIによるレポート

The US Food and Drug Administration (FDA) has approved mitapivat (brand name Aqvesme) for treating anaemia in adults with thalassaemia, working by improving red blood cell energy. The twice-daily pill can be taken by patients who need regular blood transfusions or those who do not. Experts say it could transform disease management in high-burden countries like India.

 

 

 

このウェブサイトはCookieを使用します

サイトを改善するための分析にCookieを使用します。詳細については、プライバシーポリシーをお読みください。
拒否