GLP-1 & incretin

Dulaglutide

A once-weekly GLP-1 receptor agonist approved for type 2 diabetes, with proven cardiovascular benefit in people at high risk.

Strong evidenceApproved drugAdd to compare
01

What it is

Dulaglutide is a long-acting GLP-1 receptor agonist engineered as a fusion protein: two copies of a GLP-1 analogue joined to an antibody fragment that keeps it circulating for days. That construction is why it is injected once a week. It is a prescription medicine (Trulicity) licensed for type 2 diabetes, and its evidence base includes a large cardiovascular outcome trial.

02

How it works

  1. 1

    Activates GLP-1 receptors on pancreatic beta cells, increasing insulin release in a glucose-dependent way.

  2. 2

    Reduces glucagon release from alpha cells when glucose is already high.

  3. 3

    Slows gastric emptying, flattening the rise in glucose after a meal.

  4. 4

    Acts on hypothalamic appetite centres to reduce hunger and food intake.

  5. 5

    The antibody-fragment carrier slows clearance, giving a half-life of roughly four to five days.

03

What it's studied for

Type 2 diabetes (AWARD trial programme)
Cardiovascular outcomes in type 2 diabetes (REWIND)
Kidney outcomes in type 2 diabetes as a secondary endpoint
Weight change as a secondary endpoint
Fatty liver disease (exploratory imaging substudies)
04

Reported and studied effects

  • HbA1c reductions of roughly 0.7 to 1.6 percentage points depending on dose and comparator
  • Modest weight loss, generally 1 to 3 kg in trials
  • A 12% relative reduction in major cardiovascular events in REWIND
  • Slower gastric emptying and lower post-meal glucose excursions

Research protocol notes

Research context only

Research context only - dulaglutide is a prescription medicine and its use is set by a doctor. Licensed dosing starts at 0.75 mg subcutaneously once weekly and may step up to 1.5, 3 or 4.5 mg weekly; trials ran from 26 weeks to over five years. This describes the label and the literature, not a dosing suggestion.

These figures are described so you can understand what researchers did. They are not a dose, a schedule, or a suggestion — and they are not a substitute for a doctor.

05

Possible side effects and contraindications

Safety profile

Possible side effects

  • Nausea, diarrhoea, vomiting and abdominal discomfort, mostly early in treatment
  • Reduced appetite
  • Injection-site reactions
  • Gallbladder disease
  • Pancreatitis (rare)
  • Hypoglycaemia when combined with insulin or a sulfonylurea

Contraindications and cautions

  • Personal or family history of medullary thyroid carcinoma
  • Multiple endocrine neoplasia syndrome type 2
  • Pregnancy
  • Prior serious hypersensitivity to the drug
  • Severe gastroparesis needs specialist assessment

A side-effect list is never complete, and these are not the only situations that warrant caution. Anything unexpected, or anything you are unsure about, should be discussed with a doctor before use.

06

Evidence assessment

Strong evidenceReplicated, large human trials
Replicated, large human trials

The AWARD randomised programme plus the REWIND cardiovascular outcome trial (nearly 10,000 participants), with regulatory approval in the EU and US.

07

References

  1. 01Gerstein et al., Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND), Lancet 2019
  2. 02European Medicines Agency - Trulicity product information

References link to published literature, regulator pages or literature indexes. Where a link points to a search, it collects the peer-reviewed work on that molecule rather than a single study.