Ofatumumab (English Wikipedia)

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

refsWebsite

Global rank English rank

32web.archive.org

1^st place

9europa.eu

68^th place

117^th place

8nih.gov

4^th place

6fda.gov

447^th place

338^th place

5doi.org

2^nd place

3canada.ca

1,712^th place

1,063^rd place

2drugs.com

399^th place

333^rd place

2medicines.org.uk

3,823^rd place

2,387^th place

2semanticscholar.org

11^th place

8^th place

2tga.gov.au

3,984^th place

2,622^nd place

1handle.net

102^nd place

76^th place

1bioprocessonline.com

low place

1medscape.com

719^th place

636^th place

1genmab.com

low place

1gsk.com

low place

1fdanews.com

low place

1epmmagazine.com

low place

1novartis.com

low place

1globenewswire.com

2,614^th place

1,549^th place

bioprocessonline.com

"Genmab To Transfer Ofatumumab From GSK To Novartis". www.bioprocessonline.com. Archived from the original on 29 September 2022. Retrieved 31 October 2022.

canada.ca

health-products.canada.ca

"Arzerra Product information 86740". Drug Product Database. 25 April 2012. Archived from the original on 22 August 2020. Retrieved 21 August 2020.
"Arzerra Product information 86741". Drug Product Database. 25 April 2012. Archived from the original on 22 August 2020. Retrieved 21 August 2020.

canada.ca

"Health product highlights 2021: Annexes of products approved in 2021". Health Canada. 3 August 2022. Archived from the original on 25 March 2024. Retrieved 25 March 2024.

doi.org

Hauser SL, Bar-Or A, Cohen JA, Comi G, Correale J, Coyle PK, et al. (August 2020). "Ofatumumab versus Teriflunomide in Multiple Sclerosis". The New England Journal of Medicine. 383 (6): 546–557. doi:10.1056/nejmoa1917246. hdl:11573/1473907. PMID 32757523. S2CID 221015936.
Arneth BM (June 2019). "Impact of B cells to the pathophysiology of multiple sclerosis". Journal of Neuroinflammation. 16 (1): 128. doi:10.1186/s12974-019-1517-1. PMC 6593488. PMID 31238945.
Lin TS (2010). "Ofatumumab: a novel monoclonal anti-CD20 antibody". Pharmacogenomics and Personalized Medicine. 3: 51–59. doi:10.2147/PGPM.S6840. PMC 3513208. PMID 23226042.
Anonymous Referee #2 (26 September 2016). "Interactive comment on "Sensitivity of the Variability of Mineral Aerosol Simulations to Meteorological Forcing Datasets" by Molly B. Smith et al". Atmospheric Chemistry and Physics. doi:10.5194/acp-2016-638-rc1.
Teeling JL, Mackus WJ, Wiegman LJ, van den Brakel JH, Beers SA, French RR, et al. (July 2006). "The biological activity of human CD20 monoclonal antibodies is linked to unique epitopes on CD20". Journal of Immunology. 177 (1): 362–371. doi:10.4049/jimmunol.177.1.362. PMID 16785532. S2CID 24974085.

drugs.com

"Ofatumumab (Arzerra) Use During Pregnancy". Drugs.com. 29 January 2020. Archived from the original on 29 November 2020. Retrieved 22 August 2020.
"Arzerra (ofatumumab) FDA Approval History". Drugs.com. 26 October 2009. Archived from the original on 1 September 2020. Retrieved 21 August 2020.

epmmagazine.com

"Novartis to transition use of Arzerra to compassionate use outside US". EPM Magazine. 22 January 2018. Archived from the original on 28 August 2021. Retrieved 21 August 2020.

europa.eu

ema.europa.eu

"Arzerra EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 8 August 2020. Retrieved 21 August 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"Kesimpta EPAR". European Medicines Agency (EMA). 25 January 2021. Archived from the original on 16 April 2021. Retrieved 16 April 2021.
"Arzerra : EPAR - Product Information" (PDF). European Medicines Agency. 7 March 2013. Archived from the original (PDF) on 4 February 2014. Retrieved 24 January 2014.
"Kesimpta EPAR" (PDF). European Medicines Agency (EMA). Archived (PDF) from the original on 21 October 2022. Retrieved 31 October 2022.
"Arzerra EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 8 August 2020. Retrieved 31 October 2022.
"Kesimpta - Summary of Product Characteristics (SPC)" (PDF). European Medicines Agency (EMA). Archived (PDF) from the original on 21 October 2022. Retrieved 31 October 2022.
"Arzerra: Withdrawn application". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 28 October 2020. Retrieved 21 August 2020.
"Arzerra: Withdrawal of the marketing authorisation in the European Union" (PDF). European Medicines Agency. 28 February 2019. Archived (PDF) from the original on 28 August 2021. Retrieved 21 August 2020.

ec.europa.eu

"Kesimpta Product information". Union Register of medicinal products. Archived from the original on 5 March 2023. Retrieved 3 March 2023.

fda.gov

accessdata.fda.gov

"Prescribing Information Kesimpta" (PDF). U.S. Food and Drug Administration (FDA). Archived (PDF) from the original on 22 April 2022. Retrieved 31 October 2022.
"Drug Approval Package:Arzerra (Ofatumumab) Injection Application: 125326". U.S. Food and Drug Administration (FDA). 21 January 2010. Archived from the original on 10 April 2021. Retrieved 21 August 2020.
"Ofatumumab (Kesimpta) FDA approval letter" (PDF). Archived (PDF) from the original on 12 April 2021. Retrieved 22 August 2020.

fda.gov

"Boxed Warning and new recommendations to decrease risk of hepatitis B". U.S. Food and Drug Administration. 21 June 2019. Archived from the original on 28 April 2020. Retrieved 11 September 2021.
"Arzerra (ofatumumab) Information". U.S. Food and Drug Administration (FDA). 3 November 2018. Archived from the original on 31 October 2022. Retrieved 31 October 2022.

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.

fdanews.com

"Novartis Withdraws Chronic Leukemia Drug Arzerra From Non-U.S. Markets". FDANews. 30 January 2018. Archived from the original on 28 August 2021. Retrieved 21 August 2020.

genmab.com

ir.genmab.com

"Genmab - Global Agreement for Humax-CD20". Genmab - Global Agreement for Humax-CD20. Retrieved 31 October 2022.

globenewswire.com

"Genmab Announces Plan to Transition Arzerra (ofatumumab) to an Oncology Access Program for Chronic Lymphocytic Leukemia Patients in the U.S. Copenhagen Stock Exchange:GEN" (Press release). Genmab A/S. 20 August 2020. Archived from the original on 16 April 2021. Retrieved 16 April 2021 – via GlobeNewswire.

gsk.com

"GSK completes divestment of rights to ofatumumab for auto-immune indications to Novartis". GSK (Press release). Archived from the original on 7 October 2022. Retrieved 31 October 2022.

handle.net

hdl.handle.net

Hauser SL, Bar-Or A, Cohen JA, Comi G, Correale J, Coyle PK, et al. (August 2020). "Ofatumumab versus Teriflunomide in Multiple Sclerosis". The New England Journal of Medicine. 383 (6): 546–557. doi:10.1056/nejmoa1917246. hdl:11573/1473907. PMID 32757523. S2CID 221015936.

medicines.org.uk

"Arzerra (acetate formulation) -Summary of Product Characteristics (SPC)". electronic Medicines Compendium. GlaxoSmithKline UK. 27 November 2013. Archived from the original on 4 March 2016. Retrieved 24 January 2014.
"Kesimpta 20 mg solution for injection in pre-filled pen - Patient Information Leaflet (PIL)". (emc). 14 April 2021. Archived from the original on 16 April 2021. Retrieved 16 April 2021.

medscape.com

reference.medscape.com

"Arzerra (ofatumumab) dosing, indications, interactions, and more". Medscape Reference. WebMD. Archived from the original on 2 February 2014. Retrieved 24 January 2014.

nih.gov

pubmed.ncbi.nlm.nih.gov

Hauser SL, Bar-Or A, Cohen JA, Comi G, Correale J, Coyle PK, et al. (August 2020). "Ofatumumab versus Teriflunomide in Multiple Sclerosis". The New England Journal of Medicine. 383 (6): 546–557. doi:10.1056/nejmoa1917246. hdl:11573/1473907. PMID 32757523. S2CID 221015936.
Arneth BM (June 2019). "Impact of B cells to the pathophysiology of multiple sclerosis". Journal of Neuroinflammation. 16 (1): 128. doi:10.1186/s12974-019-1517-1. PMC 6593488. PMID 31238945.
Lin TS (2010). "Ofatumumab: a novel monoclonal anti-CD20 antibody". Pharmacogenomics and Personalized Medicine. 3: 51–59. doi:10.2147/PGPM.S6840. PMC 3513208. PMID 23226042.
Teeling JL, Mackus WJ, Wiegman LJ, van den Brakel JH, Beers SA, French RR, et al. (July 2006). "The biological activity of human CD20 monoclonal antibodies is linked to unique epitopes on CD20". Journal of Immunology. 177 (1): 362–371. doi:10.4049/jimmunol.177.1.362. PMID 16785532. S2CID 24974085.

dailymed.nlm.nih.gov

"Arzerra- ofatumumab injection, solution". DailyMed. 22 June 2020. Archived from the original on 14 February 2021. Retrieved 21 August 2020.
"Kesimpta- ofatumumab injection, solution". DailyMed. 20 August 2020. Archived from the original on 14 February 2021. Retrieved 23 August 2020.

ncbi.nlm.nih.gov

Arneth BM (June 2019). "Impact of B cells to the pathophysiology of multiple sclerosis". Journal of Neuroinflammation. 16 (1): 128. doi:10.1186/s12974-019-1517-1. PMC 6593488. PMID 31238945.
Lin TS (2010). "Ofatumumab: a novel monoclonal anti-CD20 antibody". Pharmacogenomics and Personalized Medicine. 3: 51–59. doi:10.2147/PGPM.S6840. PMC 3513208. PMID 23226042.

novartis.com

"FDA approves Novartis Kesimpta (ofatumumab), the first and only self-administered, targeted B-cell therapy for patients with relapsing multiple sclerosis" (Press release). Novartis. 20 August 2020. Archived from the original on 24 September 2020. Retrieved 21 August 2020.

semanticscholar.org

api.semanticscholar.org

Hauser SL, Bar-Or A, Cohen JA, Comi G, Correale J, Coyle PK, et al. (August 2020). "Ofatumumab versus Teriflunomide in Multiple Sclerosis". The New England Journal of Medicine. 383 (6): 546–557. doi:10.1056/nejmoa1917246. hdl:11573/1473907. PMID 32757523. S2CID 221015936.
Teeling JL, Mackus WJ, Wiegman LJ, van den Brakel JH, Beers SA, French RR, et al. (July 2006). "The biological activity of human CD20 monoclonal antibodies is linked to unique epitopes on CD20". Journal of Immunology. 177 (1): 362–371. doi:10.4049/jimmunol.177.1.362. PMID 16785532. S2CID 24974085.

tga.gov.au

"AusPAR: Ofatumumab". Therapeutic Goods Administration (TGA). 19 August 2021. Archived from the original on 11 September 2021. Retrieved 10 September 2021.

ebs.tga.gov.au

"Summary for ARTG Entry:196945 Arzerra ofatumumab (rmc) 100mg/5mL injection concentrate vial". Therapeutic Goods Administration (TGA). Archived from the original on 28 August 2021. Retrieved 23 August 2020.

web.archive.org

"Ofatumumab (Arzerra) Use During Pregnancy". Drugs.com. 29 January 2020. Archived from the original on 29 November 2020. Retrieved 22 August 2020.
"AusPAR: Ofatumumab". Therapeutic Goods Administration (TGA). 19 August 2021. Archived from the original on 11 September 2021. Retrieved 10 September 2021.
"Summary for ARTG Entry:196945 Arzerra ofatumumab (rmc) 100mg/5mL injection concentrate vial". Therapeutic Goods Administration (TGA). Archived from the original on 28 August 2021. Retrieved 23 August 2020.
"Health product highlights 2021: Annexes of products approved in 2021". Health Canada. 3 August 2022. Archived from the original on 25 March 2024. Retrieved 25 March 2024.
"Arzerra (acetate formulation) -Summary of Product Characteristics (SPC)". electronic Medicines Compendium. GlaxoSmithKline UK. 27 November 2013. Archived from the original on 4 March 2016. Retrieved 24 January 2014.
"Kesimpta 20 mg solution for injection in pre-filled pen - Patient Information Leaflet (PIL)". (emc). 14 April 2021. Archived from the original on 16 April 2021. Retrieved 16 April 2021.
"Arzerra- ofatumumab injection, solution". DailyMed. 22 June 2020. Archived from the original on 14 February 2021. Retrieved 21 August 2020.
"Kesimpta- ofatumumab injection, solution". DailyMed. 20 August 2020. Archived from the original on 14 February 2021. Retrieved 23 August 2020.
"Arzerra EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 8 August 2020. Retrieved 21 August 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"Kesimpta EPAR". European Medicines Agency (EMA). 25 January 2021. Archived from the original on 16 April 2021. Retrieved 16 April 2021.
"Kesimpta Product information". Union Register of medicinal products. Archived from the original on 5 March 2023. Retrieved 3 March 2023.
"Arzerra : EPAR - Product Information" (PDF). European Medicines Agency. 7 March 2013. Archived from the original (PDF) on 4 February 2014. Retrieved 24 January 2014.
"Genmab To Transfer Ofatumumab From GSK To Novartis". www.bioprocessonline.com. Archived from the original on 29 September 2022. Retrieved 31 October 2022.
"Boxed Warning and new recommendations to decrease risk of hepatitis B". U.S. Food and Drug Administration. 21 June 2019. Archived from the original on 28 April 2020. Retrieved 11 September 2021.
"Kesimpta EPAR" (PDF). European Medicines Agency (EMA). Archived (PDF) from the original on 21 October 2022. Retrieved 31 October 2022.
"Prescribing Information Kesimpta" (PDF). U.S. Food and Drug Administration (FDA). Archived (PDF) from the original on 22 April 2022. Retrieved 31 October 2022.
"Arzerra EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 8 August 2020. Retrieved 31 October 2022.
"Arzerra (ofatumumab) Information". U.S. Food and Drug Administration (FDA). 3 November 2018. Archived from the original on 31 October 2022. Retrieved 31 October 2022.
"Kesimpta - Summary of Product Characteristics (SPC)" (PDF). European Medicines Agency (EMA). Archived (PDF) from the original on 21 October 2022. Retrieved 31 October 2022.
"Arzerra (ofatumumab) dosing, indications, interactions, and more". Medscape Reference. WebMD. Archived from the original on 2 February 2014. Retrieved 24 January 2014.
"Drug Approval Package:Arzerra (Ofatumumab) Injection Application: 125326". U.S. Food and Drug Administration (FDA). 21 January 2010. Archived from the original on 10 April 2021. Retrieved 21 August 2020.
"Arzerra (ofatumumab) FDA Approval History". Drugs.com. 26 October 2009. Archived from the original on 1 September 2020. Retrieved 21 August 2020.
"Arzerra Product information 86740". Drug Product Database. 25 April 2012. Archived from the original on 22 August 2020. Retrieved 21 August 2020.
"Arzerra Product information 86741". Drug Product Database. 25 April 2012. Archived from the original on 22 August 2020. Retrieved 21 August 2020.
"GSK completes divestment of rights to ofatumumab for auto-immune indications to Novartis". GSK (Press release). Archived from the original on 7 October 2022. Retrieved 31 October 2022.
"Arzerra: Withdrawn application". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 28 October 2020. Retrieved 21 August 2020.
"Arzerra: Withdrawal of the marketing authorisation in the European Union" (PDF). European Medicines Agency. 28 February 2019. Archived (PDF) from the original on 28 August 2021. Retrieved 21 August 2020.
"Novartis Withdraws Chronic Leukemia Drug Arzerra From Non-U.S. Markets". FDANews. 30 January 2018. Archived from the original on 28 August 2021. Retrieved 21 August 2020.
"Novartis to transition use of Arzerra to compassionate use outside US". EPM Magazine. 22 January 2018. Archived from the original on 28 August 2021. Retrieved 21 August 2020.
"FDA approves Novartis Kesimpta (ofatumumab), the first and only self-administered, targeted B-cell therapy for patients with relapsing multiple sclerosis" (Press release). Novartis. 20 August 2020. Archived from the original on 24 September 2020. Retrieved 21 August 2020.
"Ofatumumab (Kesimpta) FDA approval letter" (PDF). Archived (PDF) from the original on 12 April 2021. Retrieved 22 August 2020.
"Genmab Announces Plan to Transition Arzerra (ofatumumab) to an Oncology Access Program for Chronic Lymphocytic Leukemia Patients in the U.S. Copenhagen Stock Exchange:GEN" (Press release). Genmab A/S. 20 August 2020. Archived from the original on 16 April 2021. Retrieved 16 April 2021 – via GlobeNewswire.