EMA
approval
· 2026-02-19
EMA Authorised: Dovprela (previously Pretomanid FGK) (pretomanid) — Mylan IRE Healthcare Limited
Summary
The European Medicines Agency authorised Dovprela (pretomanid) for tuberculosis, including multidrug-resistant tuberculosis, with orphan medicine designation fo…
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Tuberculosis, Multidrug-Resistant. MAH: Mylan IRE Healthcare Limited. Decision date: 19/01/2026. Orphan medicine