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Trulicity

Dulaglutide

A once-weekly GLP-1 injection for type-2 diabetes.

Generic name
Dulaglutide
Brand name
Trulicity
Route
Subcutaneous
Marketed by
Eli Lilly
FDA pharmacologic class
GLP-1 Receptor Agonist; Glucagon-like Peptide-1 (GLP-1) Agonists
First FDA approval
18 Sep 2014

Where Dulaglutide is approved

All regulators →

Of the three regulators tracked here, the first to approve Dulaglutide was the US, on 18 Sep 2014. It is approved in 3 of the 3 regulators tracked here.

USUnited States (FDA)
18 Sep 2014
Trulicity
BLA125469 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
21 Nov 2014
Trulicity
EMA product page
First centralised authorisation
CACanada (Health Canada)
10 Nov 2015
Trulicity
Notice of Compliance 17461
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

What health systems spend on Dulaglutide

All medicines →
ENNHS England
£42.7m
523,816 items dispensed, Aug 2025 to Jul 2026
-20% on the previous 12 months
Net ingredient cost, community prescriptions
USUS Medicaid
$1.93bn
1,940,795 prescriptions in 2025 · Trulicity
-10% on 2024
Amount Medicaid reimbursed, before rebates

From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.

How Dulaglutide works

All drug targets →
  • Glucagon-like peptide 1 receptor agonist Agonist
    Target: GLP1R glucagon like peptide 1 receptor
    ChEMBL only
Diseases it has been tested for in clinical trials, by furthest phase
  • Chronic kidney diseasePhase 3
  • Middle cerebral artery stenosisPhase 2/3
  • PolydipsiaPhase 2
  • Cystic fibrosis-related diabetesPhase 2
  • Nicotine dependencePhase 2
  • Type 1 diabetes mellitusPhase 2
  • Irregular menstruationPhase 1/2
  • Insulin secretionPhase 1

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL2108027, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3), ligand 7638, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Dulaglutide

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • IE
    Ireland: 4 products on the HPRA list
    Each product record links to the HPRA, which publishes the leaflet and SmPC.
  • EU
    European Union: Trulicity
    EMA product information: package leaflet and summary of product characteristics in every EU language.
  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Reference identifiers for Dulaglutide

ATC code
A10BJ05
ChEMBL
CHEMBL2108027
DrugBank
DB09045
CAS number
923950-08-7
FDA UNII
WTT295HSY5
Wikidata
Q21011228
Wikipedia
Dulaglutide

Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.

What Trulicity is used for

TRULICITY ® is indicated: As an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients 10 years of age and older with type 2 diabetes mellitus. To reduce the risk of major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke) in adults with type 2 diabetes mellitus who have established cardiovascular disease or multiple cardiovascular risk factors. TRULICITY ® is a glucagon-like peptide-1 (GLP-1) receptor agonist indicated ( 1 ): As an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients 10 years of age and older with type 2 diabetes mellitus. To reduce the risk of major adverse cardiovascular events in adults with type 2 diabetes mellitus who have established cardiovascular disease or multiple cardiovascular risk factors. Limitations of Use: Has not been studied …

How it works

12.1 Mechanism of Action TRULICITY contains dulaglutide, which is a human GLP-1 receptor agonist with 90% amino acid sequence homology to endogenous human GLP-1 (7-37). Dulaglutide activates the GLP-1 receptor, a membrane-bound cell-surface receptor coupled to adenylyl cyclase in pancreatic beta cells. Dulaglutide increases intracellular cyclic AMP (cAMP) in beta cells leading to glucose-dependent insulin release. Dulaglutide also decreases glucagon secretion and slows gastric emptying.

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How this page is built

The facts on this page are pulled directly from official U.S. FDA datasets — they are not written from memory. Each field below names the dataset it came from, so you can check it yourself.

Plain-English summaries and drug-class explainers are written and reviewed by Sreepriya Prasannan (MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany). Data is retrieved automatically from the sources above and cross-checked with AI-assisted verification (Anthropic's Claude) — brand and generic names are matched against the exact FDA product record so that a combination product or a different formulation cannot be mistaken for the drug on this page. An editor reviews the result before publication. We describe this in full in our editorial standards and corrections policy. The FDA data on this page was last retrieved on 9 Oct 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.