EU/3/25/3031 - orphan designation for treatment of limb-girdle muscular dystrophy
adeno-associated virus sector serotype rh74 containing the human SGCG gene
OrphanHuman
Overview
This medicine was designated as an orphan medicine for the treatment of limb-girdle muscular dystrophy in the European Union on 27 February 2025.
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:
Key facts
- Active substance
- adeno-associated virus sector serotype rh74 containing the human SGCG gene
- Intended use
- Treatment of limb-girdle muscular dystrophy
- Orphan designation status
- Positive
- EU designation number
- EU/3/25/3031
- Date of designation
- Sponsor
Sarepta Therapeutics Ireland Limited
EMA list of opinions on orphan medicinal product designation
EMA publishes information on orphan medicinal product designation adopted by the Committee for Orphan Medicinal Products (COMP) on the IRIS online platform:
Patients' organisations
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.
EU register of orphan medicines
The list of medicines that have received an orphan designation in the EU is available on the European Commission's website: