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    GLP-1

    Retatrutide

    None of the 30 tracked EU+ jurisdictions lists Retatrutide as authorised. This page summarises approval status, brands, shortages and recent regulatory changes by country.

    Protocol detail references

    Related regulatory compounds

    Country-by-country approval and availability

    30 EU+ jurisdictions covered.

    🇩🇪
    Germany

    No approved pharmaceutical form available.

    Phase III
    France

    No approved pharmaceutical form available.

    Phase III
    🇮🇹
    Italy

    No approved pharmaceutical form available.

    Phase III
    🇪🇸
    Spain

    No approved pharmaceutical form available.

    Phase III
    🇳🇱
    Netherlands

    No approved pharmaceutical form available.

    Phase III
    🇬🇷
    Greece

    No approved pharmaceutical form available.

    Phase III
    🇸🇪
    Sweden

    No approved pharmaceutical form available.

    Phase III
    🇩🇰
    Denmark

    No approved pharmaceutical form available.

    Phase III
    🇫🇮
    Finland

    No approved pharmaceutical form available.

    Phase III
    🇦🇹
    Austria

    No approved pharmaceutical form available.

    Phase III
    🇧🇪
    Belgium

    No approved pharmaceutical form available.

    Phase III
    🇱🇺
    Luxembourg

    No approved pharmaceutical form available.

    Phase III
    🇵🇹
    Portugal

    No approved pharmaceutical form available.

    Phase III
    🇮🇪
    Ireland

    No approved pharmaceutical form available.

    Phase III
    🇵🇱
    Poland

    No approved pharmaceutical form available.

    Phase III
    🇨🇿
    Czech Republic

    No approved pharmaceutical form available.

    Phase III
    🇸🇰
    Slovakia

    No approved pharmaceutical form available.

    Phase III
    🇭🇺
    Hungary

    No approved pharmaceutical form available.

    Phase III
    🇸🇮
    Slovenia

    No approved pharmaceutical form available.

    Phase III
    🇭🇷
    Croatia

    No approved pharmaceutical form available.

    Phase III
    🇪🇪
    Estonia

    No approved pharmaceutical form available.

    Phase III
    🇱🇻
    Latvia

    No approved pharmaceutical form available.

    Phase III
    🇱🇹
    Lithuania

    No approved pharmaceutical form available.

    Phase III
    🇷🇴
    Romania

    No approved pharmaceutical form available.

    Phase III
    🇧🇬
    Bulgaria

    No approved pharmaceutical form available.

    Phase III
    🇨🇾
    Cyprus

    No approved pharmaceutical form available.

    Phase III
    🇲🇹
    Malta

    No approved pharmaceutical form available.

    Phase III
    🇬🇧
    United Kingdom

    No approved pharmaceutical form available.

    Phase III
    🇨🇭
    Switzerland

    No approved pharmaceutical form available.

    Phase III
    🇳🇴
    Norway

    No approved pharmaceutical form available.

    Phase III

    Updates for Retatrutide

    • 2026-03-19 · 🇪🇺 EU

      Retatrutide: TRIUMPH-4 published — 28.7% weight loss

      March 2026: full Phase 3 TRIUMPH-4 results from Eli Lilly were published, showing 28.7% average body weight loss — the highest ever recorded in an obesity clinical trial. Seven additional TRIUMPH trials are expected throughout 2026, with NDA filing to the FDA expected in late 2026.

    • 2025-08-15 · 🇪🇺 EU

      Retatrutide: remains investigational — Phase 3 ongoing

      Retatrutide (Eli Lilly, LY3437943) remains unapproved by FDA/EMA. TRIUMPH (obesity) and TRANSCEND (cardiovascular) Phase 3 programs are ongoing with regulatory submission expected from 2026 onwards.

    • 2024-10-08 · 🇪🇺 EU

      Retatrutide: Phase III interim data published

      Eli Lilly published Phase III interim showing average -24% body weight at 48 weeks.

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