Elivaldogene autotemcel

Elivaldogene autotemcel
Clinical data
Trade namesSkysona
Other namesLenti-D, eli-cel
Routes of
administration
Intravenous
ATC code
  • None
Legal status
Legal status
  • EU: Rx-only [1]
Identifiers
DrugBank
UNII
KEGG

Elivaldogene autotemcel, sold under the brand name Skysona, is a gene therapy used to treat cerebral adrenoleukodystrophy (CALD).[1] It is being developed by Bluebird bio.

Elivaldogene autotemcel is made specifically for each recipient, using the recipient's hematopoietic stem cells.[2]

History

Elivaldogene autotemcel was designated an orphan drug by the European Medicines Agency (EMA) in 2012.[3]

Elivaldogene autotemcel was granted orphan drug, rare pediatric disease, and breakthrough therapy designations by the U.S. Food and Drug Administration (FDA).[4]

On 20 May 2021, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended the granting of a marketing authorization for elivaldogene autotemcel.[5][2] The applicant was Bluebird Bio (Netherlands) B.V.[2] In July 2021, the European Commission approved elivaldogene autotemcel under the tradename Skysona for CALD patients who have certain genetic mutations and don't have a sibling who is a match for a stem cell transplant.[6]

Society and culture

Names

Elivaldogene autotemcel is the recommended international nonproprietary name (INN).[7]

References

  1. 1 2 "Skysona EPAR". European Medicines Agency. Retrieved 22 November 2021.
  2. 1 2 3 "Skysona: Pending EC decision". European Medicines Agency (EMA). 21 May 2021. Retrieved 1 June 2021. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  3. "EU/3/12/1003". European Medicines Agency (EMA). Retrieved 1 June 2021.
  4. "Bluebird Bio Presents Long-Term Data for elivaldogene autotemcel (eli-cel, Lenti-D) Gene Therapy for Cerebral Adrenoleukodystrophy (CALD)" (Press release). Bluebird Bio. 15 March 2021. Retrieved 1 June 2021 via Business Wire.
  5. "First gene therapy to treat children with rare inherited neurological disease". European Medicines Agency (EMA) (Press release). 21 May 2021. Retrieved 1 June 2021. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  6. Fidler, Ben (21 July 2021). "Bluebird, with little fanfare, is first to bring a second gene therapy to market". Industry Dive. Retrieved 22 November 2021.
  7. World Health Organization (2020). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 83" (PDF). WHO Drug Information. 34 (1).

Further reading


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