Arsenic trioxide Accord
arsenic trioxide
Table of contents
Overview
Arsenic trioxide Accord is used to treat adults (aged 18 years or over) with acute promyelocytic leukaemia (APL), a rare form of leukaemia (cancer of the white blood cells) caused by a genetic ‘translocation’ (when there is a swap of genes between two chromosomes). The translocation affects the way the white blood cells grow, and as a result they lack the ability to use retinoic acid (vitamin A). Patients with APL are normally treated with retinoids (substances derived from vitamin A).
Arsenic trioxide Accord is used in:
- Patients with newly diagnosed low or intermediate risk APL where it is used together with the medicine all-trans-retinoic acid.
- Patients with APL whose disease has not responded to previous treatment with a retinoid and cancer medicines, or when their disease has come back after this type of treatment.
Arsenic trioxide Accord contains the active substance arsenic trioxide and is a ‘generic medicine’. This means that Arsenic trioxide Accord contains the same active substance and works in the same way as a ‘reference medicine’ already authorised in the EU called Trisenox.
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Arsenic trioxide Accord : EPAR - Medicine overview (PDF/94.13 KB)
First published: 26/11/2019
EMA/520484/2019 -
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Arsenic trioxide Accord : EPAR - Risk -management-plan summary (PDF/102.37 KB)
First published: 26/11/2019
Authorisation details
Product details | |
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Name |
Arsenic trioxide Accord
|
Agency product number |
EMEA/H/C/005175
|
Active substance |
Arsenic trioxide
|
International non-proprietary name (INN) or common name |
arsenic trioxide
|
Therapeutic area (MeSH) |
Leukemia, Promyelocytic, Acute
|
Anatomical therapeutic chemical (ATC) code |
L01XX27
|
Generic |
This is a generic medicine, which is developed to be the same as a medicine that has already been authorised, called the reference medicine. A generic medicine contains the same active substance(s) as the reference medicine, and is used at the same dose(s) to treat the same disease(s). For more information, see Generic and hybrid medicines. |
Publication details | |
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Marketing-authorisation holder |
Accord Healthcare S.L.U.
|
Revision |
5
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Date of issue of marketing authorisation valid throughout the European Union |
14/11/2019
|
Contact address |
Accord Healthcare S.L.U. |
Product information
10/05/2022 Arsenic trioxide Accord - EMEA/H/C/005175 - IB/0007
This medicine’s product information is available in all official EU languages.
Select ‘available languages’ to access the language you need.
Product information documents contain:
- summary of product characteristics (annex I);
- manufacturing authorisation holder responsible for batch release (annex IIA);
- conditions of the marketing authorisation (annex IIB);
- labelling (annex IIIA);
- package leaflet (annex IIIB).
You can find product information documents for centrally authorised human medicines on this website. For centrally authorised veterinary medicines authorised or updated from February 2022, see the Veterinary Medicines Information website.
Pharmacotherapeutic group
Antineoplastic agents
Therapeutic indication
Arsenic trioxide is indicated for induction of remission, and consolidation in adult patients with:
- Newly diagnosed low-to-intermediate risk acute promyelocytic leukaemia (APL) (white blood cell count, ≤ 10 x 103/μl) in combination with all-trans-retinoic acid (ATRA)
- Relapsed/refractory acute promyelocytic leukaemia (APL)(Previous treatment should have included a retinoid and chemotherapy) characterised by the presence of the t(15;17) translocation and/or the presence of the promyelocytic leukaemia/retinoic-acid-receptor-alpha (PML/RAR-alpha) gene.
The response rate of other acute myelogenous leukaemia subtypes to arsenic trioxide has not been examined.