EMA Authorised: Takhzyro (lanadelumab) — Takeda Pharmaceuticals International AG Ireland Branch

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Summary

EU authorization for Takhzyro (lanadelumab) by Takeda for hereditary angioedema, with orphan designation and accelerated assessment.

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Diseases / indications

• Hereditary Angioedema

Drugs mentioned

• Takhzyro (lanadelumab)

Snippet

Status: Authorised. Therapeutic area: Angioedemas, Hereditary. MAH: Takeda Pharmaceuticals International AG Ireland Branch. Decision date: 28/05/2026. Orphan medicine. Accelerated assessment