Boehringer Ingelheim reports Phase III SYNCHRONIZE-2 data showing survodutide weight reduction and glycemic improvements in adults with obesity and type 2 diabetes

The 76-week trial met its co-primary endpoints, with up to 13.1% average weight loss using the efficacy estimand and improvements in HbA1c, waist circumference and insulin sensitivity.

Boehringer Ingelheim reported positive Phase III SYNCHRONIZE-2 results for investigational survodutide (BI 456906) in adults living with obesity or overweight and type 2 diabetes. After 76 weeks, participants achieved up to 13.1% average weight loss using the efficacy estimand versus 3.1% with placebo, while the trial also showed improvements in HbA1c, waist circumference and insulin sensitivity. The company said the results were presented at the 62nd Annual Meeting of the European Association for the Study of Diabetes and simultaneously published in The New England Journal of Medicine; survodutide has not been approved for use and its efficacy and safety have not been established.

SYNCHRONIZE-2 met its co-primary endpoints, with up to 13.1% average weight loss using the efficacy estimand after 76 weeks versus 3.1% with placebo.
Survodutide-treated participants showed improvements in HbA1c, waist circumference and insulin-sensitivity measures alongside weight reduction.
The most commonly reported adverse events were gastrointestinal and mostly mild to moderate; GI-related treatment discontinuation was 18% with survodutide versus 1.2% with placebo.
Survodutide remains investigational and has not been approved for use; its efficacy and safety have not been established.

What did the SYNCHRONIZE-2 Phase III trial report?

The trial met its co-primary endpoints. After 76 weeks, average weight loss reached up to 13.1% using the efficacy estimand versus 3.1% with placebo, and up to 79.3% of adults treated with survodutide achieved at least 5% body weight reduction versus 32.7% with placebo.
What cardiometabolic changes were reported with survodutide?

The release reports an HbA1c reduction of up to 1.21% from a 7.4% baseline, reductions in waist circumference, improvements in fasting glucose and insulin-sensitivity measures, and a higher proportion of participants reverting to normoglycemia during treatment compared with placebo.
Is survodutide approved for use?

No. Survodutide is an investigational glucagon/GLP-1 receptor dual agonist and has not been approved for use; its efficacy and safety have not been established.
What adverse events were most commonly reported in SYNCHRONIZE-2?

The most commonly reported adverse events were gastrointestinal events, mostly mild to moderate in severity, including nausea, vomiting, diarrhea and constipation. Treatment discontinuation due to gastrointestinal adverse events was 18% with survodutide and 1.2% with placebo.

(PRESS RELEASE) INGELHEIM, Germany, 2-Oct-2026 — /EuropaWire/ —

The Phase III SYNCHRONIZE-2 trial met its co-primary endpoints, with participants achieving body weight reduction of up to 13.1% after 76 weeks of survodutide treatment versus 3.1% in the placebo arm among people with type 2 diabetes, a population in which weight loss is typically more challenging.¹
Detailed findings indicated improvements in key cardiometabolic markers, including an HbA1c reduction of up to 1.21% from a 7.4% baseline, together with improvements in waist circumference and insulin sensitivity.¹
The results were presented at the 62nd Annual Meeting of the European Association for the Study of Diabetes (EASD) and simultaneously published in The New England Journal of Medicine, alongside new findings from a SYNCHRONIZE-1 body-composition sub study.^1,2,3

Boehringer Ingelheim reported positive results from the Phase III SYNCHRONIZE-2 trial evaluating the investigational glucagon/GLP-1 receptor dual agonist survodutide (BI 456906) in adults living with obesity or overweight and type 2 diabetes (T2D).¹ The study met its co-primary endpoints of percentage change in body weight from baseline and body weight reduction of at least 5% from baseline under both the treatment-regimen* and efficacy estimands†.¹ Following 76 weeks of treatment, average sustained weight loss reached up to 13.1% using the efficacy estimand, compared with 3.1% in the placebo arm (p<0.0001)‡.¹ Up to 79.3% of adults receiving survodutide achieved body weight reduction of at least 5% using the efficacy estimand, versus 32.7% with placebo (p<0.0001).¹ Full SYNCHRONIZE-2 findings were presented at the 62nd Annual Meeting of the European Association for the Study of Diabetes (EASD) and simultaneously published in The New England Journal of Medicine.^1,2

Secondary endpoint findings also showed improvements in cardiometabolic health markers. Participants treated with survodutide recorded an HbA1c reduction of up to 1.21% using the efficacy estimand, compared with a 0.03% reduction for placebo (p<0.0001) from a baseline HbA1c of 7.4%.¹ Waist circumference decreased by 11.1 cm under the efficacy estimand versus 3.5 cm with placebo (p<0.0001).^1,4 Insulin sensitivity also improved, reflected in lower fasting glucose and favorable changes in insulin resistance (HOMA-IR) and insulin secretion (HOMA-β) versus placebo. During treatment, up to 29.5% of participants receiving survodutide reverted to normoglycemia (HbA1c<5.7%) compared with 4.0% in the placebo arm under the efficacy estimand.¹ Boehringer Ingelheim said these findings support the potential of glucagon/GLP-1 dual agonism to improve metabolic health, including glycemic control, in people living with obesity and T2D.

“Obesity and type 2 diabetes are deeply intertwined, with excess weight increasing the risk of T2D. For people living with these conditions, sustained weight loss is often a biological struggle rather than a lack of willpower,” said Dr. Sean Wharton, M.D., PharmD, Coordinating Investigator of the SYNCHRONIZE-2 trial. “These results are encouraging because, in obesity medicine, clinicians increasingly recognize the opportunity to address multiple interconnected health conditions together. Seeing improvements in glycemic control and insulin sensitivity alongside weight loss provides evidence that tackling obesity can positively influence broader metabolic health. This brings new optimism to people seeking more effective ways to improve their overall health.”

T2D and obesity are interrelated metabolic conditions, with the liver playing a central role in disease progression.^5,6 Survodutide, an investigational glucagon/GLP-1 receptor (GCGR) dual agonist, is designed to target multiple underlying metabolic drivers by improving glycemic control, reducing appetite and supporting reductions in liver fat.^7,8,9 Although glucagon is traditionally associated with raising blood glucose, the company said survodutide’s dual mechanism may help improve insulin sensitivity and glucose management through its effects on liver fat reduction.^7,10 The specific balance of GCGR and GLP-1R agonism may help preserve glycemic control. Survodutide has not been approved for use, and its efficacy and safety have not been established.

“The growing body of evidence from our SYNCHRONIZE Phase III program continues to strengthen our understanding of survodutide’s potential in people living with obesity, including those with type 2 diabetes. The SYNCHRONIZE-2 results demonstrate meaningful weight loss alongside improvements in glycemic control and other key markers of metabolic health, reinforcing our belief that obesity should be addressed as a complex chronic disease with interconnected health consequences,” said Shashank Deshpande, Chairman of the Board of Managing Directors and Head of Human Pharma, Boehringer Ingelheim. “We remain committed to advancing innovative treatment approaches that address the diverse needs of people living with obesity across different stages of disease and risk profiles.”

As expected with GLP-1 based therapies and in line with previously reported survodutide trials, the most commonly reported adverse events in SYNCHRONIZE-2 were gastrointestinal (GI) events and were mostly mild to moderate in severity.¹ The more frequent events were nausea, vomiting, diarrhea and constipation.¹ Treatment discontinuation due to GI adverse events occurred in 18% of people receiving survodutide compared with 1.2% in the placebo arm.¹

Discontinuations generally occurred during dose escalation, when the study protocol allowed limited flexibility for managing adverse events.¹ Current and upcoming trials allow more flexible, patient-centered titration strategies intended to support tolerability.^11,12

Additional analyses from a SYNCHRONIZE-1 sub study involving people living with obesity without T2D (n=75) were presented with the SYNCHRONIZE-2 results.³ MRI-based body-composition assessments showed preferential reductions in metabolically active visceral and liver fat.³ The overall pattern suggested a shift away from excessive abdominal fat accumulation. Building on previously reported lean-mass findings,¹³ a new muscle-specific analysis found that muscle accounted for no more than 10% of total tissue lost.³ The reductions in visceral and liver fat appeared largely independent of the degree of weight reduction achieved, suggesting that these benefits may extend beyond weight reduction alone.³

Taken together, the SYNCHRONIZE findings suggest survodutide may address multiple dimensions of metabolic dysfunction by delivering weight loss and glycemic improvements while reducing visceral and liver fat. Adipose tissue reduction was greater than the loss of lean body mass, indicating that most body weight reduction was attributable to the loss of adipose tissue.¹³

Boehringer Ingelheim’s survodutide development program spans obesity and related metabolic conditions, MASH and T2D.^{11,12,14,15,16,17,18,19,20} The company expects to present results from its cardiovascular outcomes trial, SYNCHRONIZE-CVOT, later this year to further elucidate survodutide’s cardiovascular safety profile and understanding of its role across the cardiometabolic disease continuum.¹⁷ Boehringer Ingelheim has also launched the Phase III SYNCHRONIZE-T2D trial (NCT07754461) to further investigate survodutide’s effect on glycemic control in adults with T2D who manage their condition with diet and exercise alone or in combination with diabetes medications, including insulin.²⁰

* The treatment-regimen estimand is the estimated treatment effect, regardless of whether the patient adheres to the treatment, discontinues, or initiates other therapies.

†The efficacy estimand is the estimated treatment effect assuming patients remained on treatment for the entire study duration.

‡P-values for efficacy estimand are nominal.

Notes to editors

About obesity and overweight

More than one billion people around the world are living with obesity today (1 in 8 of us) – and by 2030, that number could be more than double what it was in 2010.²¹ Overweight and obesity are complex chronic conditions involving abnormal or excessive fat accumulation that present a risk to a person’s overall health.²²

About survodutide (BI 456906)

Survodutide is a glucagon/GLP-1 receptor dual agonist that activates both the glucagon and GLP-1 receptors, which play a role in controlling metabolic functions.^7,9,23 Survodutide is an investigational agent and has not been approved for use; its efficacy and safety has not been established. It is being evaluated in a robust Phase III clinical development program, including the SYNCHRONIZE studies for people living with overweight or obesity,^{14,15,16,17,18,19} the LIVERAGE studies for people living with MASH and fibrosis,^11,12 and SYNCHRONIZE T2D for adults with T2D.²⁰

Survodutide has potential to treat adults with non-cirrhotic MASH and moderate or advanced fibrosis (stages 2 or 3) and has been recognized by the U.S. FDA, which granted it:

Fast Track designation in May 2021 and;²⁴
Breakthrough Therapy designation in September 2024.²⁵

Survodutide’s potential to treat adults with MASH and fibrosis has also been recognized by:

the European Medicines Agency (EMA), through acceptance to its PRIME scheme in November 2023 and;²⁶
the Center for Drug Evaluation of China’s National Medical Products Administration (NMPA) which granted it Breakthrough Therapy designation in June 2024 and;
the Taiwan Food and Drug Administration which granted it Breakthrough Designation in September 2024.

Survodutide is licensed to Boehringer Ingelheim from Zealand Pharma, with Boehringer solely responsible for development and commercialization globally. Survodutide is part of Boehringer Ingelheim’s research and development portfolio in the cardiovascular, renal and metabolic disease areas.

About the SYNCHRONIZE-2 trial (NCT06066528)

This is a Phase III, double-blind, placebo-controlled 76-week efficacy and safety trial of survodutide among 755 adults living with obesity or overweight and type 2 diabetes.¹⁵ Participants received a weekly injection of survodutide at either a 3.6 mg or 6.0 mg dose, or placebo.¹⁵ The co-primary endpoints of the trial are the percentage change in body weight from baseline to Week 76, and an achievement of body weight reduction ≥5% from baseline to Week 76.¹⁵

There are 22 secondary endpoints, including, achievement of ≥10, ≥15%, and ≥20% body weight reduction, and absolute changes from baseline to Week 76 in:¹⁵

Body weight
Glycosylated hemoglobin A1c (HbA1c)
Waist circumference
Blood pressure
Eating Behavior PRO
Body Mass Index (BMI)
Fasting plasma glucose (FPG)

About the SYNCHRONIZE program

Survodutide has been evaluated in three other global Phase III studies for people living with overweight or obesity.

SYNCHRONIZE-1 enrolled adults without type 2 diabetes.¹⁴
SYNCHRONIZE-MASLD enrolled adults with a confirmed or presumed diagnosis of MASH.¹⁶
SYNCHRONIZE-CVOT enrolled adults with cardiovascular disease, chronic kidney disease, or with risk factors for cardiovascular disease.¹⁷

Survodutide has also been explored in two Phase III in-market trials:

SYNCHRONIZE-JP in Japan and SYNCHRONIZE-CN in China are exploring survodutide for sub-populations of people living with obesity.^18,19 SYNCHRONIZE-JP explores the relative change in liver fat and body composition parameters from baseline to Week 76 when treated with survodutide versus placebo, as a secondary endpoint.¹⁸

As part of the broader evidence program, a set of Phase IIIb studies are being advanced to address key unmet needs in people living with obesity and real-world care, including:

SYNCHRONIZE-HERA will evaluate survodutide in women’s health.
ELEVATE-LIVER will assess the impact of survodutide in the preservation of cardiac function and structure in people living with metabolic dysfunction-associated steatotic liver disease (MASLD) or early metabolic dysfunction-associated steatohepatitis (MASH).
SYNCHRONIZE-START will examine real-world titration approaches, including treatment initiation and switching from GLP-1 RAs, with a focus on tolerability.

About SYNCHRONIZE-T2D

SYNCHRONIZE-T2D will investigate the effect of survodutide on improving glycemic control in adults with T2D who are managing their condition with diet and exercise alone or in combination with diabetes medications, including insulin.²⁰

About LIVERAGE and LIVERAGE-Cirrhosis

LIVERAGE and LIVERAGE-Cirrhosis are global Phase III clinical trials investigating the efficacy and safety of survodutide in adults with MASH and fibrosis stages 2 or 3 and in those with compensated MASH cirrhosis (fibrosis stage 4), respectively.^11,12

LIVERAGE will enroll approximately 1,800 adults, and LIVERAGE-Cirrhosis will enroll approximately 1,590 adults. In each trial, participants are randomized to receive weekly injections of either survodutide, reaching a maximum dose, or placebo.^11,12

About Boehringer Ingelheim

Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry’s top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,300 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at http://www.boehringer-ingelheim.com.

Boehringer Ingelheim’s Intended Audiences Notice

This press release is issued from our Corporate Headquarters in Ingelheim, Germany and is intended to provide information about our global business. Please be aware that information relating to the approval status and labels of approved products may vary from country to country, and a country-specific press release on this topic may have been issued in the countries where we do business.

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