Onasemnogene abeparvovec
| Gene therapy | |
|---|---|
| Target gene | SMN1 |
| Vector | Adeno-associated virus serotype 9 |
| Clinical data | |
| Trade names | Zolgensma |
| Other names | AVXS-101, onasemnogene abeparvovec-xioi |
| AHFS/Drugs.com | Professional Drug Facts |
| License data | |
| Pregnancy category | |
| Routes of administration | Intravenous |
| ATC code | |
| Legal status | |
| Legal status | |
| Identifiers | |
| CAS Number | |
| PubChem CID | |
| DrugBank | |
| UNII | |
| KEGG | |
Onasemnogene abeparvovec, sold under the brand name Zolgensma, is a gene therapy used to treat spinal muscular atrophy (SMA),[5][6] a disease causing muscle function loss in children. It involves a one-time infusion of the medication into a vein.[5] It works by providing a new copy of the SMN gene that produces the SMN protein.[5]
SMA stems from an SMN1 gene mutation, causing SMN protein deficiency vital for motor neuron survival. Onasemnogene abeparvovec, a biologic drug utilizing AAV9 virus capsids containing an SMN1 transgene, is administered to motor neurons, boosting SMN protein levels. Common side effects include vomiting and elevated liver enzymes, while more severe reactions involve liver issues and low platelet count.[5][7]
Developed by AveXis and acquired by Novartis, onasemnogene abeparvovec gained various FDA designations and approvals globally. Controversies included data manipulation concerns and delayed reporting to regulatory agencies. Onasemnogene abeparvovec's price is high, earning it the title of the world's most expensive medication at the time of commercial approval.[9] This has later been exceeded by other gene therapies like Hemgenix. Several countries such as Japan,[10][11] Netherlands,[12] Canada,[13] Brazil[14] and others negotiated a lower price for Zolgensma for their public healthcare systems.
- ^ a b "Zolgensma". Therapeutic Goods Administration (TGA). 10 March 2021. Archived from the original on 9 September 2021. Retrieved 8 September 2021.
- ^ a b "AusPAR: Onasemnogene abeparvovec". Therapeutic Goods Administration (TGA). 22 April 2021. Archived from the original on 9 September 2021. Retrieved 8 September 2021.
- ^ "Summary Basis of Decision (SBD) for Zolgensma". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- ^ "Zolgensma 2 x 1013 vector genomes/mL solution for infusion - Summary of Product Characteristics (SmPC)". (emc). 30 June 2020. Archived from the original on 28 October 2020. Retrieved 30 July 2020.
- ^ a b c d e "Zolgensma- onasemnogene abeparvovec-xioi kit full prescribing information". DailyMed. 24 May 2019. Archived from the original on 19 November 2019. Retrieved 18 November 2019.
- ^ a b Cite error: The named reference
FDA Zolgensmawas invoked but never defined (see the help page). - ^ a b "Zolgensma EPAR". European Medicines Agency (EMA). 24 March 2020. Archived from the original on 17 July 2020. Retrieved 30 July 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- ^ "Zolgensma Product information". Union Register of medicinal products. Retrieved 3 March 2023.
- ^ Cite error: The named reference
pharmanews18401was invoked but never defined (see the help page). - ^ Cite error: The named reference
:1was invoked but never defined (see the help page). - ^ Cite error: The named reference
:2was invoked but never defined (see the help page). - ^ "Archive | BeNeLuxA". beneluxa.org. Retrieved 25 April 2025.
- ^ Wexler M (14 October 2021). "Novartis Wraps Zolgensma Price, Access Negotiations for SMA in Canada". smanewstoday.com. Retrieved 25 April 2025.
- ^ Ivama-Brummell AM, Wagner AK, Pepe VL, Naci H (March 2022). "Ultraexpensive gene therapies, industry interests and the right to health: the case of onasemnogene abeparvovec in Brazil". BMJ Global Health. 7 (3): e008637. doi:10.1136/bmjgh-2022-008637. PMC 8915307. PMID 35277426.