Page contentsPage contents Key facts Decision Key facts Active substance teprotumumab Therapeutic area Ophthalmology Decision number P/0381/2023 PIP number EMEA-001973-PIP02-23 Pharmaceutical form(s) Powder for concentrate for solution for infusionSolution for injection Condition(s) / indication(s) Treatment of thyroid eye disease Route(s) of administration Intravenous useSubcutaneous use Contact for public enquiries Amgen Europe B.V. E-mail: medinfointernational@amgen.comTel. +44 (0)1223 420305 Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 07/09/2023 Compliance check done No Decision P/0381/2023 : EMA decision of 7 September 2023 on the granting of a product specific waiver for teprotumumab, (EMEA-001973-PIP02-23)Reference Number: EMA/389821/2023 English (EN) (189.59 KB - PDF)First published: 19/09/2024 View Share this page