List of gene therapies (English Wikipedia)
Analysis of information sources in references of the Wikipedia article "List of gene therapies" in English language version.
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businesswire.com
- "Sarepta Therapeutics Announces FDA Approval of Elevidys, the First Gene Therapy to Treat Duchenne Muscular Dystrophy" (Press release). Sarepta Therapeutics. 22 June 2023. Retrieved 22 June 2023 – via Business Wire.
europa.eu
ema.europa.eu
- "First gene therapy to treat severe haemophilia A" (Press release). European Medicines Agency (EMA). 24 June 2022. Archived from the original on 26 June 2022. Retrieved 26 June 2022.
- "Roctavian: Pending EC decision". European Medicines Agency (EMA). 23 June 2022. Archived from the original on 26 June 2022. Retrieved 26 June 2022.
ec.europa.eu
- "Roctavian". Union Register of medicinal products. 25 August 2022. Retrieved 6 September 2022.
fda.gov
- "FDA approves CAR-T cell therapy to treat adults with certain types of large B-cell lymphoma" (Press release). U.S. Food and Drug Administration (FDA). 24 March 2020. Retrieved 16 December 2022.
- "FDA Approves First Topical Gene Therapy for Treatment of Wounds in Patients with Dystrophic Epidermolysis Bullosa". U.S. Food and Drug Administration (FDA) (Press release). 19 May 2023. Retrieved 28 May 2023.
This article incorporates text from this source, which is in the public domain. - "FDA Approves First Cell-Based Gene Therapy to Treat Adult and Pediatric Patients with Beta-thalassemia Who Require Regular Blood Transfusions" (Press release). U.S. Food and Drug Administration (FDA). 17 August 2022. Retrieved 16 December 2022.
- "FDA Approves First Cell-Based Gene Therapy For Adult Patients with Relapsed or Refractory MCL" (Press release). U.S. Food and Drug Administration (FDA). 24 July 2020. Retrieved 24 July 2020.
- "FDA approves brexucabtagene autoleucel for relapsed or refractory B-cell precursor acute lymphoblastic leukemia". U.S. Food and Drug Administration (FDA). 1 October 2021. Retrieved 2 October 2021.
- "FDA approves ciltacabtagene autoleucel for relapsed or refractory multiple myeloma". U.S. Food and Drug Administration (FDA). 7 March 2022. Retrieved 16 March 2022.
- "FDA Approves First Gene Therapy for Treatment of Certain Patients with Duchenne Muscular Dystrophy" (Press release). U.S. Food and Drug Administration (FDA). 22 June 2023. Retrieved 22 June 2023. This article incorporates text from this source, which is in the public domain.
- "Skysona". U.S. Food and Drug Administration (FDA). 24 October 2022. Retrieved 16 December 2022.
- "FDA Approves First Gene Therapy to Treat Adults with Hemophilia B" (Press release). U.S. Food and Drug Administration (FDA). 22 November 2022. Retrieved 16 December 2022.
- "FDA Approves First Gene Therapies to Treat Patients with Sickle Cell Disease". U.S. Food and Drug Administration (FDA) (Press release). 8 December 2023. Archived from the original on 8 December 2023. Retrieved 8 December 2023.
- "Abecma". U.S. Food and Drug Administration (FDA). 21 April 2021. Retrieved 16 December 2022.
- "FDA Approves First Gene Therapy for the Treatment of High-Risk, Non-Muscle-Invasive Bladder Cancer" (Press release). U.S. Food and Drug Administration (FDA). 16 December 2022. Retrieved 16 December 2022.
- "FDA approves innovative gene therapy to treat pediatric patients with spinal muscular atrophy, a rare disease and leading genetic cause of infant mortality" (Press release). U.S. Food and Drug Administration (FDA). 24 March 2020. Retrieved 16 December 2022.
- "Imlygic (talimogene laherparepvec)". U.S. Food and Drug Administration (FDA). 6 July 2022. Retrieved 16 December 2022.
- "FDA approves tisagenlecleucel for B-cell ALL and tocilizumab for cytokine release syndrome". U.S. Food and Drug Administration (FDA). 30 August 2017. Retrieved 16 December 2022.
- "FDA approves novel gene therapy to treat patients with a rare form of inherited vision loss". U.S. Food and Drug Administration (Press release). 24 March 2020. Retrieved 16 December 2022.
web.archive.org
- "FDA Approves First Gene Therapies to Treat Patients with Sickle Cell Disease". U.S. Food and Drug Administration (FDA) (Press release). 8 December 2023. Archived from the original on 8 December 2023. Retrieved 8 December 2023.
- "First gene therapy to treat severe haemophilia A" (Press release). European Medicines Agency (EMA). 24 June 2022. Archived from the original on 26 June 2022. Retrieved 26 June 2022.
- "Roctavian: Pending EC decision". European Medicines Agency (EMA). 23 June 2022. Archived from the original on 26 June 2022. Retrieved 26 June 2022.