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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.

Amycretin

Novo Nordisk · GLP-1 and amylin receptor agonist (single molecule) · Peptide · Investigational
Region
Q2 2026Q3 2026Q4 2026Q1 2027Q2 2027Q3 2027Q4 2027Q1 2028
USFDA
TodayNo verified events yet
UKMHRA
No verified events yet
EUEMA / European Commission
No verified events yet

No verified events recorded 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.

No verified records yet for Amycretin. See coverage.

All Amycretin records (accessible list)

Amycretin

Investigational single-molecule GLP-1 and amylin agonist in subcutaneous and oral formulations; results are formulation-specific.

United Kingdom

No verified events recorded yet. Regulator: MHRA.

United States

No verified events recorded yet. Regulator: FDA.

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.