Landmark Trials in Endocrinology & Metabolism

Practice-changing trials

Practice-changing landmark trials in endocrinology and metabolism, organized for rapid clinical review, exam preparation, teaching, and evidence-based patient care.

Landmark Cardiovascular Outcomes

Look AHEAD: Intensive Lifestyle Intervention Does Not Reduce Cardiovascular Events in Obese Type 2 Diabetes

The Look AHEAD trial demonstrated that intensive lifestyle intervention targeting weight loss in overweight or obese adults with type 2 diabetes did not reduce cardiovascular events over 9.6 years despite clear differences in weight, fitness, and glycaemic control, establishing a critical negative result that informed the rationale for pharmacological obesity treatment with greater weight loss efficacy.

Landmark GLP-1 Receptor Agonists

SCALE: Liraglutide 3.0 mg for Obesity — The Trial That Opened the GLP-1 Weight Management Era

The SCALE trial established liraglutide 3.0 mg as the first GLP-1 receptor agonist approved for chronic weight management, demonstrating a mean weight reduction of 8.0% versus 2.6% with placebo and a 79% reduction in progression from prediabetes to type 2 diabetes in a 160-week extension analysis, setting the clinical and regulatory template for GLP-1 receptor agonist obesity pharmacotherapy.

Landmark Cardiovascular Outcomes

SELECT: Semaglutide 2.4 mg Reduces Cardiovascular Events by 20% in Obese Non-Diabetic Patients with CVD

The SELECT trial demonstrated that semaglutide 2.4 mg reduces 3-point MACE by 20% in overweight or obese adults with pre-existing cardiovascular disease and no diabetes, becoming the first obesity pharmacotherapy trial to demonstrate a hard cardiovascular endpoint benefit and establishing GLP-1 receptor agonism as a cardiovascular intervention in non-diabetic obesity.

Landmark GLP-1 Receptor Agonists

SURMOUNT-1: Tirzepatide Achieves up to 20.9% Weight Loss in Obesity — Entering Surgical Territory

SURMOUNT-1 demonstrated that tirzepatide, a dual GIP/GLP-1 receptor agonist, produces dose-dependent mean weight reductions of 15.0–20.9% in adults with obesity without type 2 diabetes, with 57% of participants at the 15 mg dose losing 20% or more of body weight, setting a new pharmacological efficacy benchmark comparable in magnitude to bariatric surgery outcomes.

Landmark GLP-1 Receptor Agonists

STEP 1: Semaglutide 2.4 mg Produces Unprecedented 14.9% Weight Loss in Obesity Without Diabetes

STEP 1 demonstrated that once-weekly semaglutide 2.4 mg produced a mean weight reduction of 14.9% compared with 2.4% with placebo in adults with obesity without type 2 diabetes, with a third of participants losing more than 20% of body weight, setting a new benchmark for pharmacological weight management and preceding the cardiovascular outcomes evidence from SELECT.

Landmark Diabetes Complications

DAPA-CKD: Dapagliflozin Reduces Kidney Failure by 39% in Albuminuric CKD Regardless of Diabetes Status

DAPA-CKD demonstrated that dapagliflozin reduced the composite of a sustained 50% or greater eGFR decline, end-stage kidney disease, or renal or cardiovascular death by 39% in patients with albuminuric CKD with or without type 2 diabetes, extending nephroprotective SGLT2 inhibition beyond diabetic nephropathy to a broad CKD population for the first time.

Landmark Heart Failure & Renal Protection

EMPEROR-Reduced: Empagliflozin Reduces Heart Failure Hospitalisation and Preserves Renal Function in HFrEF

EMPEROR-Reduced confirmed that empagliflozin reduces cardiovascular death or hospitalisation for heart failure by 25% in patients with HFrEF irrespective of diabetes status, while also demonstrating a 50% reduction in a renal composite outcome and a markedly slower rate of eGFR decline, adding critical confirmatory evidence for SGLT2 inhibitors as standard-of-care in HFrEF.

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