Oxbryta is a medicine used to treat haemolytic anaemia (excess breakdown of red blood cells) in patients aged 12 years and older who have sickle cell disease. Oxbryta can be given on its own or together with another medicine for sickle cell disease called hydroxycarbamide. Sickle cell disease is a genetic disease where individuals produce an abnormal form of haemoglobin (the protein in red blood cells that carries oxygen). The red blood cells become rigid and sticky, and change from being disc-shaped to being crescent-shaped (like a sickle). Sickle cell disease is rare, and Oxbryta was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 18 November 2016. Further information on the orphan designation can be found here: [ema.europa.eu/medicines/human/orphan-designations/eu-3-16-1769](/en/medicines/human/orphan-designations/eu-3-16-1769). Oxbryta contains the active substance voxelotor.
Therapeutic Indication
### Therapeutic indication Oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (SCD) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.
Therapeutic Area (MeSH)
ATC Code
B06AX03
ATC Item
voxelotor
Pharmacotherapeutic Group
Other hematological agents
Active Substance (Summary)
INN / Common Names
| Substance | CAS | Monograph |
|---|---|---|
| Voxelotor | N/A | 沃克沙妥 |
EMA Name
Oxbryta
Medicine Name
Oxbryta
Aliases
N/A