Tisagenlecleucel (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Tisagenlecleucel" in English language version.

refsWebsite

Global rank English rank

27web.archive.org

1^st place

8fda.gov

447^th place

338^th place

4tga.gov.au

3,984^th place

2,622^nd place

4nih.gov

4^th place

3nytimes.com

7^th place

2doi.org

2^nd place

1hres.ca

low place

1europa.eu

68^th place

117^th place

1aacr.org

low place

1fiercebiotech.com

low place

8,828^th place

1harvard.edu

18^th place

17^th place

1npr.org

92^nd place

72^nd place

1lifescienceleader.com

low place

1ascopost.com

low place

1theguardian.com

12^th place

11^th place

1nice.org.uk

3,258^th place

2,666^th place

1genengnews.com

low place

6,625^th place

1reuters.com

49^th place

47^th place

1biopharma-reporter.com

low place

1outsourcing-pharma.com

low place

1handle.net

102^nd place

76^th place

aacr.org

leadingdiscoveries.aacr.org

Clark H (5 January 2024). "Dr. Carl H. June: Forging a Path for Cancer Cell Therapy". Leading Discoveries Magazine. Retrieved 5 June 2024.

ascopost.com

"FDA Expands Tisagenlecleucel Approval - The ASCO Post". www.ascopost.com. Archived from the original on 27 November 2018. Retrieved 11 June 2019.

biopharma-reporter.com

"Cryoport's CEO on cell therapies' market 'robust demand'". biopharma-reporter.com. 22 April 2019. Archived from the original on 24 October 2020. Retrieved 18 October 2019.

doi.org

Awasthi R, Maier HJ, Zhang J, Lim S (2023). "Kymriah® (Tisagenlecleucel) – an overview of the clinical development journey of the first approved CAR-T therapy". Human Vaccines & Immunotherapeutics. 19 (1). doi:10.1080/21645515.2023.2210046. PMC 10294746. PMID 37185251.
Ledford H (July 2017). "Engineered cell therapy for cancer gets thumbs up from FDA advisers". Nature. 547 (7663): 270. Bibcode:2017Natur.547..270L. doi:10.1038/nature.2017.22304. PMID 28726836.

europa.eu

ema.europa.eu

"Kymriah EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 21 October 2020. Retrieved 15 August 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.

fda.gov

"Kymriah (tisagenlecleucel)". U.S. Food and Drug Administration. 7 July 2022. Archived from the original on 19 November 2022. Retrieved 19 November 2022.
"FDA approval brings first gene therapy to the United States". U.S. Food & Drug Administration (FDA) (Press release). Archived from the original on 24 April 2019. Retrieved 31 August 2017.
"BLA 125646 Tisagenlecleucel - Novartis Briefing document to FDA ODAC" (PDF). Food and Drug Administration. Archived (PDF) from the original on 16 July 2017. Retrieved 16 July 2017.
"FDA approves tisagenlecleucel". U.S. Food and Drug Administration. 31 May 2022. Archived from the original on 5 December 2023. Retrieved 1 June 2022. This article incorporates text from this source, which is in the public domain.
"FDA Requires Boxed Warning for T cell Malignancies Following Treatment with BCMA-Directed or CD19-Directed Autologous Chimeric Antigen Receptor (CAR) T cell Immunotherapies". U.S. Food and Drug Administration (FDA). 18 April 2024. Archived from the original on 19 April 2024. Retrieved 19 April 2024. This article incorporates text from this source, which is in the public domain.
"Kymriah (tisagenlecleucel)". U.S. Food and Drug Administration (FDA). 1 April 2018. Archived from the original on 21 December 2019. Retrieved 1 April 2020.
"FDA approval brings first gene therapy to the United States". U.S. Food and Drug Administration (FDA) (Press release). Archived from the original on 24 April 2019. Retrieved 6 September 2017.

nctr-crs.fda.gov

"FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 October 2023.

fiercebiotech.com

"Novartis gets second CAR-T candidate FDA 'breakthrough' tag". www.fiercebiotech.com. Fierce Biotech. 18 April 2017. Archived from the original on 20 April 2017. Retrieved 19 April 2017.

genengnews.com

"FDA Panel Unanimously Recommends Approval for Novartis' CAR T-Cell Therapy CTL019". GEN. GEN Genetic Engineering & Biotechnology News. 13 July 2017. Archived from the original on 16 July 2017. Retrieved 16 July 2017.

handle.net

hdl.handle.net

World Health Organization (2018). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 79". WHO Drug Information. 32 (1). hdl:10665/330941.

harvard.edu

ui.adsabs.harvard.edu

Ledford H (July 2017). "Engineered cell therapy for cancer gets thumbs up from FDA advisers". Nature. 547 (7663): 270. Bibcode:2017Natur.547..270L. doi:10.1038/nature.2017.22304. PMID 28726836.

hres.ca

hpr-rps.hres.ca

"Summary Basis of Decision (SBD) for Kymriah". Health Canada. 23 October 2014. Archived from the original on 31 May 2022. Retrieved 29 May 2022.

lifescienceleader.com

Harris E (27 November 2019). "Challenges Facing The Cell And Gene Sector's Regulation Landscape". Life Science Leader. Pennsylvania, United States: VertMarkets. Archived from the original on 14 December 2019. Retrieved 13 December 2019. After Kymriah (Novartis), Yescarta (Gilead), and Luxturna (Spark) were approved in the U.S. in 2017, they were subsequently approved in 2018 in the EU. Kymriah also has received approval in Australia and an additional indication in the U.S.{{cite magazine}}: CS1 maint: overridden setting (link)

nice.org.uk

"Overview | Tisagenlecleucel for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more systemic therapies | Guidance | NICE". www.nice.org.uk. 13 March 2019. Archived from the original on 28 July 2021. Retrieved 3 August 2021.

nih.gov

pubmed.ncbi.nlm.nih.gov

Awasthi R, Maier HJ, Zhang J, Lim S (2023). "Kymriah® (Tisagenlecleucel) – an overview of the clinical development journey of the first approved CAR-T therapy". Human Vaccines & Immunotherapeutics. 19 (1). doi:10.1080/21645515.2023.2210046. PMC 10294746. PMID 37185251.
Ledford H (July 2017). "Engineered cell therapy for cancer gets thumbs up from FDA advisers". Nature. 547 (7663): 270. Bibcode:2017Natur.547..270L. doi:10.1038/nature.2017.22304. PMID 28726836.

dailymed.nlm.nih.gov

"Kymriah- tisagenlecleucel injection, suspension". DailyMed. 14 June 2019. Archived from the original on 22 October 2020. Retrieved 1 April 2020.

ncbi.nlm.nih.gov

Awasthi R, Maier HJ, Zhang J, Lim S (2023). "Kymriah® (Tisagenlecleucel) – an overview of the clinical development journey of the first approved CAR-T therapy". Human Vaccines & Immunotherapeutics. 19 (1). doi:10.1080/21645515.2023.2210046. PMC 10294746. PMID 37185251.

npr.org

Stein R (12 July 2017). "'Living Drug' That Fights Cancer By Harnessing The Immune System Clears Key Hurdle". NPR. Archived from the original on 8 February 2018. Retrieved 13 July 2017.{{cite news}}: CS1 maint: overridden setting (link)

nytimes.com

"FDA Panel Backs Novartis' Pioneering New Cancer Gene Therapy". The New York Times. Reuters. 12 July 2017. Archived from the original on 14 July 2017.
Grady D (12 July 2017). "F.D.A. Panel Recommends Approval for Gene-Altering Leukemia Treatment". The New York Times. Archived from the original on 22 November 2017. Retrieved 1 April 2020.{{cite web}}: CS1 maint: overridden setting (link)
Grady D (30 August 2017). "F.D.A. Approves First Gene-Altering Leukemia Treatment, Costing $475,000". The New York Times. Archived from the original on 28 January 2018. Retrieved 6 September 2017.{{cite news}}: CS1 maint: overridden setting (link)

outsourcing-pharma.com

"Cryoport talks compliance, biopharma expansion, and Brexit". outsourcing-pharma.com. 13 November 2018. Archived from the original on 30 November 2020. Retrieved 18 October 2019.

reuters.com

Miller J (28 November 2019). "Novartis's $90 million Swiss factory to help solve cell therapy bottleneck". Reuters. Archived from the original on 30 November 2019. Retrieved 1 December 2019.{{cite news}}: CS1 maint: overridden setting (link)

tga.gov.au

"Updates to the Prescribing Medicines in Pregnancy database". Therapeutic Goods Administration (TGA). 12 May 2022. Archived from the original on 3 April 2022. Retrieved 13 May 2022.
"KYMRIAH (Novartis Pharmaceuticals Australia Pty LTD) | Therapeutic Goods Administration (TGA)". Archived from the original on 2 January 2024. Retrieved 2 January 2024.
"KYMRIAH (Novartis Pharmaceuticals Australia Pty LTD) | Therapeutic Goods Administration (TGA)". Archived from the original on 2 January 2024. Retrieved 2 January 2024.
"KYMRIAH (Novartis Pharmaceuticals Australia Pty LTD) | Therapeutic Goods Administration (TGA)". Archived from the original on 2 January 2024. Retrieved 2 January 2024.

theguardian.com

Sarah Boseley (5 September 2018). "NHS to treat young cancer patients with expensive 'game changer' drug". The Guardian. Archived from the original on 4 September 2018. Retrieved 5 September 2018.

web.archive.org

"Updates to the Prescribing Medicines in Pregnancy database". Therapeutic Goods Administration (TGA). 12 May 2022. Archived from the original on 3 April 2022. Retrieved 13 May 2022.
"KYMRIAH (Novartis Pharmaceuticals Australia Pty LTD) | Therapeutic Goods Administration (TGA)". Archived from the original on 2 January 2024. Retrieved 2 January 2024.
"KYMRIAH (Novartis Pharmaceuticals Australia Pty LTD) | Therapeutic Goods Administration (TGA)". Archived from the original on 2 January 2024. Retrieved 2 January 2024.
"KYMRIAH (Novartis Pharmaceuticals Australia Pty LTD) | Therapeutic Goods Administration (TGA)". Archived from the original on 2 January 2024. Retrieved 2 January 2024.
"Summary Basis of Decision (SBD) for Kymriah". Health Canada. 23 October 2014. Archived from the original on 31 May 2022. Retrieved 29 May 2022.
"Kymriah- tisagenlecleucel injection, suspension". DailyMed. 14 June 2019. Archived from the original on 22 October 2020. Retrieved 1 April 2020.
"Kymriah (tisagenlecleucel)". U.S. Food and Drug Administration. 7 July 2022. Archived from the original on 19 November 2022. Retrieved 19 November 2022.
"Kymriah EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 21 October 2020. Retrieved 15 August 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"FDA approval brings first gene therapy to the United States". U.S. Food & Drug Administration (FDA) (Press release). Archived from the original on 24 April 2019. Retrieved 31 August 2017.
"BLA 125646 Tisagenlecleucel - Novartis Briefing document to FDA ODAC" (PDF). Food and Drug Administration. Archived (PDF) from the original on 16 July 2017. Retrieved 16 July 2017.
"FDA approves tisagenlecleucel". U.S. Food and Drug Administration. 31 May 2022. Archived from the original on 5 December 2023. Retrieved 1 June 2022. This article incorporates text from this source, which is in the public domain.
"FDA Panel Backs Novartis' Pioneering New Cancer Gene Therapy". The New York Times. Reuters. 12 July 2017. Archived from the original on 14 July 2017.
"FDA Requires Boxed Warning for T cell Malignancies Following Treatment with BCMA-Directed or CD19-Directed Autologous Chimeric Antigen Receptor (CAR) T cell Immunotherapies". U.S. Food and Drug Administration (FDA). 18 April 2024. Archived from the original on 19 April 2024. Retrieved 19 April 2024. This article incorporates text from this source, which is in the public domain.
Grady D (12 July 2017). "F.D.A. Panel Recommends Approval for Gene-Altering Leukemia Treatment". The New York Times. Archived from the original on 22 November 2017. Retrieved 1 April 2020.{{cite web}}: CS1 maint: overridden setting (link)
"Novartis gets second CAR-T candidate FDA 'breakthrough' tag". www.fiercebiotech.com. Fierce Biotech. 18 April 2017. Archived from the original on 20 April 2017. Retrieved 19 April 2017.
Stein R (12 July 2017). "'Living Drug' That Fights Cancer By Harnessing The Immune System Clears Key Hurdle". NPR. Archived from the original on 8 February 2018. Retrieved 13 July 2017.{{cite news}}: CS1 maint: overridden setting (link)
"Kymriah (tisagenlecleucel)". U.S. Food and Drug Administration (FDA). 1 April 2018. Archived from the original on 21 December 2019. Retrieved 1 April 2020.
"FDA approval brings first gene therapy to the United States". U.S. Food and Drug Administration (FDA) (Press release). Archived from the original on 24 April 2019. Retrieved 6 September 2017.
Harris E (27 November 2019). "Challenges Facing The Cell And Gene Sector's Regulation Landscape". Life Science Leader. Pennsylvania, United States: VertMarkets. Archived from the original on 14 December 2019. Retrieved 13 December 2019. After Kymriah (Novartis), Yescarta (Gilead), and Luxturna (Spark) were approved in the U.S. in 2017, they were subsequently approved in 2018 in the EU. Kymriah also has received approval in Australia and an additional indication in the U.S.{{cite magazine}}: CS1 maint: overridden setting (link)
Grady D (30 August 2017). "F.D.A. Approves First Gene-Altering Leukemia Treatment, Costing $475,000". The New York Times. Archived from the original on 28 January 2018. Retrieved 6 September 2017.{{cite news}}: CS1 maint: overridden setting (link)
"FDA Expands Tisagenlecleucel Approval - The ASCO Post". www.ascopost.com. Archived from the original on 27 November 2018. Retrieved 11 June 2019.
Sarah Boseley (5 September 2018). "NHS to treat young cancer patients with expensive 'game changer' drug". The Guardian. Archived from the original on 4 September 2018. Retrieved 5 September 2018.
"Overview | Tisagenlecleucel for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more systemic therapies | Guidance | NICE". www.nice.org.uk. 13 March 2019. Archived from the original on 28 July 2021. Retrieved 3 August 2021.
"FDA Panel Unanimously Recommends Approval for Novartis' CAR T-Cell Therapy CTL019". GEN. GEN Genetic Engineering & Biotechnology News. 13 July 2017. Archived from the original on 16 July 2017. Retrieved 16 July 2017.
Miller J (28 November 2019). "Novartis's $90 million Swiss factory to help solve cell therapy bottleneck". Reuters. Archived from the original on 30 November 2019. Retrieved 1 December 2019.{{cite news}}: CS1 maint: overridden setting (link)
"Cryoport's CEO on cell therapies' market 'robust demand'". biopharma-reporter.com. 22 April 2019. Archived from the original on 24 October 2020. Retrieved 18 October 2019.
"Cryoport talks compliance, biopharma expansion, and Brexit". outsourcing-pharma.com. 13 November 2018. Archived from the original on 30 November 2020. Retrieved 18 October 2019.