Page contentsKey factsDecisionRelated contentKey facts Invented name Vabysmo Active Substance Faricimab Therapeutic area Eye disorders Decision number P/0006/2024 PIP number EMEA-002817-PIP05-23 Pharmaceutical form(s) Solution for injection Condition(s) / indication(s) Treatment of choroidal neovascularisation secondary to pathologic myopia Route(s) of administration Intravitreal use Contact for public enquiries Roche Registration GmbH E-mail: global.eu_regulatory_office@roche.comTel: +41 616879411 Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 12/01/2024DecisionP/0006/2024 : EMA decision of 12 January 2024 on the granting of a product-specific waiver for faricimab (Vabysmo), (EMEA-002817-PIP05-23)AdoptedReference Number: EMA/8520/2024 English (EN) (220.6 KB - PDF)First published: 17/03/2025ViewRelated contentVabysmoShare this page