Page contents Key factsDecisionRelated medicine informationKey facts Invented name Ultomiris Active Substance ravulizumab Therapeutic area Uro-nephrology Decision number P/0388/2023 PIP number EMEA-001943-PIP06-23 Pharmaceutical form(s) Concentrate for solution for infusion Condition(s) / indication(s) Prevention of kidney injury in high-risk patients with chronic kidney disease undergoing cardiopulmonary bypass Route(s) of administration Intravenous use Contact for public enquiries Alexion Europe SASE-mail: pip.enquiries.eu@alexion.comTel: +33 147100615 Decision type W: decision granting a waiver in all age groups for all conditions or indications DecisionP/0388/2023 : EMA decision of 7 September 2023 on the granting of a product specific waiver for ravulizumab (Ultomiris), (EMEA-001943-PIP06-23)Reference Number: EMA/389665/2023 English (EN) (211.61 KB - PDF)First published: 19/09/2024ViewRelated medicine informationUltomirisShare this page