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EMA approval · 2026-07-17

EMA Authorised: Hukyndra (adalimumab) — Stada Arzneimittel AG

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Summary

EU authorization of Hukyndra (adalimumab) by Stada Arzneimittel AG for multiple inflammatory diseases including rheumatoid arthritis and inflammatory bowel dise…

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Diseases / indications

Drugs mentioned

  • Hukyndra (adalimumab)

Snippet

Status: Authorised. Therapeutic area: Arthritis, Psoriatic;Arthritis, Juvenile Rheumatoid;Arthritis, Rheumatoid;Colitis, Ulcerative;Crohn Disease;Hidradenitis Suppurativa;Psoriasis;Spondylitis, Ankylosing;Uveitis. MAH: Stada Arzneimittel AG. Decision date: 15/07/2026