EU/3/20/2269 - orphan designation for treatment of hepatocellular carcinoma
tislelizumab
OrphanHuman
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Please note that this product was withdrawn from the Union Register of orphan medicinal products in March 2024 on request of the sponsor.
This medicine was designated as an orphan medicine for the treatment of hepatocellular carcinoma in the European Union on 22 April 2020.
This means that the developer will receive scientific and regulatory support from EMA to advance their medicine to the stage where they can apply for a marketing authorisation.
Orphan designation does not mean the medicine is available or authorised for use. All medicines, including designated orphan medicines, must be authorised before they can be marketed and made available to patients in the EU.
During the medicine's development, doctors may be able to enrol patients in clinical trials investigating the medicine. For information on ongoing clinical trials in the EU, see:
BeiGene Ireland Limited
| Date | Update |
|---|---|
| 29/11/2023 | The sponsorship was transferred to BeiGene Ireland Limited |
| 13/12/2021 | The sponsorship was transferred to Novartis Europharm Limited |
EMA publishes information on orphan medicinal product designation adopted by the Committee for Orphan Medicinal Products (COMP) on the IRIS online platform:
For contact details of patients’ organisations whose activities are targeted at rare diseases, see:
European Organisation for Rare Diseases (EURORDIS), a non-governmental alliance of patient organisations and individuals active in the field of rare diseases.
Orphanet, a database containing information on rare diseases, which includes a directory of patients’ organisations registered in Europe.
The list of medicines that have received an orphan designation in the EU is available on the European Commission's website: