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Research → decisions → accessEvidence checked 13 Sep 2026

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A clearer view of the milestones shaping peptide and GLP-1 medicines in the UK, US and EU: confirmed decisions, company targets and clearly labelled estimates, each with its source. What we track · How estimates are made.

Dulaglutide

Eli Lilly · GLP-1 receptor agonist · Peptide (Fc fusion)
Region
Q2 2026Q3 2026Q4 2026Q1 2027Q2 2027Q3 2027Q4 2027Q1 2028
UKMHRA
No verified events yet
EUEMA / European Commission
No verified events yet
Confirmed eventCompany targetRegulator targetEditorial estimateTiming unknown or undatedSafety update

Dashed line: today, 13 Sep 2026. Future windows are conditional. Approval, launch and funded access are separate milestones.

Confirmed · 18 Sep 2014United States

FDA approves Trulicity (dulaglutide) for type 2 diabetes

Original approval of BLA 125469 on 18 September 2014 for glycaemic control in adults with type 2 diabetes.

Why it matters. A once-weekly GLP-1 agonist without a weight-management indication; the workbook's 'FDA expiry 2024' refers to patent status, not to the approval, and is quarantined.

Event
Approval
Indication
Type 2 diabetes (glycaemic control) (Adjunct to diet and exercise)
Product
Trulicity, once-weekly injection
Authority
FDA
Event date
18 Sep 2014
Published
13 Sep 2026
Last checked
13 Sep 2026
Record version
v1
US Food and Drug Administration (Drugs@FDA) ↗ Report a correction Follow Dulaglutide Confirmed

All Dulaglutide records (accessible list)

Dulaglutide

Once-weekly GLP-1 receptor agonist for type 2 diabetes.

United Kingdom

No verified events recorded yet. Regulator: MHRA.

United States

· Approval Confirmed

FDA approves Trulicity (dulaglutide) for type 2 diabetes

Trulicity (once-weekly injection) · Type 2 diabetes (glycaemic control)

Original approval of BLA 125469 on 18 September 2014 for glycaemic control in adults with type 2 diabetes.

Why it matters: A once-weekly GLP-1 agonist without a weight-management indication; the workbook's 'FDA expiry 2024' refers to patent status, not to the approval, and is quarantined.

Source: US Food and Drug Administration (Drugs@FDA)

Last checked 13 Sep 2026 · Report a correction

European Union

No verified events recorded yet. Regulator: EMA / European Commission.

This list is the complete, accessible view of the tracker; the board above draws from exactly the same records. Every entry is labelled Confirmed (official record), Company target (a dated sponsor statement), Regulator target (an official decision date, not a guarantee), GLPInfo estimate (an editorial range with assumptions) or Timing unknown. An approval is never inferred from a target date passing.