EU orphan designations
Every medicine the European Commission has designated as an orphan medicine for a rare disease, on the EMA's recommendation, with its current status.
Matching designations
4 matches| Substance | Intended use | Status | Designated |
|---|---|---|---|
| 5-(3,4-Dichloro-phenyl)-N-((1R,2R)-2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamide EU/3/23/2791 |
Treatment of Alport syndrome | Active (positive) | 20 Jun 2023 |
| nicotinamide mononucleotide EU/3/23/2786 |
Treatment of sickle cell disease | Active (positive) | 20 Jun 2023 |
| N-[(2S)-2,3-dihydroxypropyl]-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide hydrochloride EU/3/10/824 |
Treatment of acute myeloid leukaemia | Withdrawn | 17 Dec 2010 |
| N-[(2S)-2,3-dihydroxypropyl]-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide hydrochloride EU/3/09/685 |
Treatment of pancreatic cancer | Withdrawn | 8 Oct 2009 |
How this page is built
Every row is copied from the EMA's orphan designations data, reproduced with acknowledgement of the source. Each substance links to its official EMA page.
- EMA orphan designations data (JSON report) ↗ active substance, intended use, EU designation number, date of designation, status and the link to each designation page
A daily job downloads the EMA's orphan designations JSON report and lists every designation, newest first. No AI drafting and no editorial pass. See our editorial standards. The the EMA data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.