Anpheros Search · Treatment

Onasemnogene abeparvovec

Also known as: Zolgensma · Itvisma

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In short

In the European Union, the product Itvisma is indicated for the treatment of 5q spinal muscular atrophy (SMA) with a bi-allelic mutation in the SMN1 gene in patients 2 years of age and older. Also in the European Union, the product Zolgensma is indicated for the treatment of patients with 5q SMA with a bi-allelic mutation in the SMN1 gene and either a clinical diagnosis of SMA Type 1 or up to 3 copies of the SMN2 gene. Onasemnogene abeparvovec is listed by the cited source as having an approved use for unspecified spinal muscular atrophy.

Source: European Medicines Agency (EMA), Itvisma — EPAR, 02/10/2026. © European Medicines Agency. · Source: European Medicines Agency (EMA), Zolgensma — EPAR, 21/08/2026. © European Medicines Agency. · Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

RxNorm
2170226 onasemnogene abeparvovec
EMA
EMEA/H/C/004750, EMEA/H/C/006498

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

EMA (EU) Itvisma

Itvisma is indicated for the treatment of 5q spinal muscular atrophy (SMA) with a bi-allelic mutation in the SMN1 gene in patients 2 years of age and older.

Source: European Medicines Agency (EMA), Itvisma — EPAR, 02/10/2026. © European Medicines Agency.

Document date: 02/10/2026 · Official document →

EMA (EU) Zolgensma

Zolgensma is indicated for the treatment of: patients with 5q spinal muscular atrophy (SMA) with a bi-allelic mutation in the SMN1 gene and a clinical diagnosis of SMA Type 1, or patients with 5q SMA with a bi-allelic mutation in the SMN1 gene and up to 3 copies of the SMN2 gene.

Source: European Medicines Agency (EMA), Zolgensma — EPAR, 21/08/2026. © European Medicines Agency.

Document date: 21/08/2026 · Official document →

Related terms in the cited sources

Has an official indication for

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What people report

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External resources

Questions

What is Onasemnogene abeparvovec approved for in the European Union?

Itvisma is indicated for the treatment of 5q spinal muscular atrophy (SMA) with a bi-allelic mutation in the SMN1 gene in patients 2 years of age and older. (Source: European Medicines Agency (EMA), Itvisma — EPAR, 02/10/2026. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Itvisma — EPAR, 02/10/2026. © European Medicines Agency.
  • Source: European Medicines Agency (EMA), Zolgensma — EPAR, 21/08/2026. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →