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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.

Approved approvedgene addition
Approved treatment At 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.

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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.