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Treatment · Beta thalassemia
Zynteglo (betibeglogene autotemcel)
An approved gene-addition therapy for transfusion-dependent beta thalassemia: the non-editing alternative to Casgevy in the same disease.
Approvedapprovedgene addition
Approved treatmentAt least one medicine using this approach has been authorised by a national regulator for this use.
Simple explanation
Zynteglo adds a working copy of the beta-globin gene into a patient's own blood stem cells using a modified virus, so their body can make normal haemoglobin again. Most people treated in its trials no longer needed blood transfusions. It treats the same condition as Casgevy by a different route.
Go deeper
Betibeglogene autotemcel delivers a functional βA-T87Q-globin gene to autologous CD34+ cells by lentiviral transduction, restoring haemoglobin production in transfusion-dependent beta thalassemia. FDA approved August 2022. Requires the same myeloablative conditioning as editing-based products.
Educational information only
This page is a reference, not medical advice. Research and regulatory status change; check the last-updated date above and confirm anything important against the primary sources listed.
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