ソトロビマブ (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ソトロビマブ" in Japanese language version.

refsWebsite

Global rank Japanese rank

6nih.gov

4^th place

24^th place

5europa.eu

68^th place

425^th place

4doi.org

2^nd place

6^th place

4fda.gov

447^th place

1,043^rd place

3tga.gov.au

3,984^th place

low place

2gsk.com

low place

5,782^nd place

2harvard.edu

18^th place

107^th place

1pmda.go.jp

6,690^th place

394^th place

1biorxiv.org

5,061^st place

4,832^nd place

biorxiv.org

Cathcart AL, Havenar-Daughton C, Lempp FA, Ma D, Schmid M, Agostini ML, Guarino B, Rosen L, Tucker H, Dillen J, Subramanian S (2021). “The dual function monoclonal antibodies VIR-7831 and VIR-7832 demonstrate potent in vitro and 3 in vivo activity against SARS-CoV-2”. bioRxiv: Preprint. doi:10.1101/2021.03.09.434607.

doi.org

Ledford H (March 2021). “COVID antibody treatments show promise for preventing severe disease”. Nature 591 (7851): 513-514. Bibcode: 2021Natur.591..513L. doi:10.1038/d41586-021-00650-7. PMID 33712752.
Cathcart AL, Havenar-Daughton C, Lempp FA, Ma D, Schmid M, Agostini ML, Guarino B, Rosen L, Tucker H, Dillen J, Subramanian S (2021). “The dual function monoclonal antibodies VIR-7831 and VIR-7832 demonstrate potent in vitro and 3 in vivo activity against SARS-CoV-2”. bioRxiv: Preprint. doi:10.1101/2021.03.09.434607.
Pinto D, Park YJ, Beltramello M, Walls AC, Tortorici MA, Bianchi S, Jaconi S, Culap K, Zatta F, De Marco A, Peter A, Guarino B, Spreafico R, Cameroni E, Case JB, Chen RE, Havenar-Daughton C, Snell G, Telenti A, Virgin HW, Lanzavecchia A, Diamond MS, Fink K, Veesler D, Corti D (July 2020). “Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody”. Nature 583 (7815): 290-295. Bibcode: 2020Natur.583..290P. doi:10.1038/s41586-020-2349-y. PMID 32422645.
Saunders KO (2019). “Conceptual Approaches to Modulating Antibody Effector Functions and Circulation Half-Life” (English). Frontiers in Immunology 10: 1296. doi:10.3389/fimmu.2019.01296. PMC 6568213. PMID 31231397.

europa.eu

ema.europa.eu

"EMA starts rolling review of sotrovimab (VIR-7831) for COVID-19". European Medicines Agency (EMA) (Press release). 7 May 2021. 2021年5月21日閲覧。 Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"EMA issues advice on use of sotrovimab (VIR-7831) for treating COVID-19". European Medicines Agency (EMA) (Press release). 21 May 2021. 2021年5月21日閲覧。 Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
"EMA starts review of VIR-7831 for treating patients with COVID-19". European Medicines Agency (EMA) (Press release). 15 April 2021. 2021年5月21日閲覧。
“Assessment Report: Use of sotrovimab for the treatment of COVID-19”. European Medicines Agency (May 2021). 2021年11月1日閲覧。
“EMA issues advice on use of sotrovimab (VIR-7831) for treating COVID-19”. European Medicines Agency (May 2021). 2021年11月1日閲覧。

fda.gov

"Coronavirus (COVID-19) Update: FDA Authorizes Additional Monoclonal Antibody for Treatment of COVID-19". U.S. Food and Drug Administration (FDA) (Press release). 26 May 2021. 2021年5月26日閲覧。 この記述には、アメリカ合衆国内でパブリックドメインとなっている記述を含む。
“Emergency Use Authorization 100: Sotrovimab”. U.S. Food and Drug Administration (FDA) (28 May 2021). 2021年11月1日閲覧。
“Fact Sheet for Healthcare Providers Emergency Use Authorization (Eua) of Sotrovimab”. U.S. Food and Drug Administration (FDA) (2021年). 2021年11月1日閲覧。
“Frequently Asked Questions on the Emergency Use Authorization of Sotrovimab”. U.S. Food and Drug Administration (FDA) (26 May 2021). 2021年11月1日閲覧。

gsk.com

jp.gsk.com

“モノクローナル抗体「ゼビュディ点滴静注液 500mg」（一般名：ソトロビマブ）、新型コロナウイルス感染症（COVID-19）に対する治療薬として製造販売承認を取得 | GSK グラクソ･スミスクライン株式会社” (英語). jp.gsk.com. 2021年11月1日閲覧。
“新型コロナウイルス感染症（COVID-19）に対する治療薬としてモノクローナル抗体ソトロビマブの製造販売承認を申請 | GSK グラクソ･スミスクライン株式会社” (英語). jp.gsk.com. 2021年11月1日閲覧。

harvard.edu

ui.adsabs.harvard.edu

Ledford H (March 2021). “COVID antibody treatments show promise for preventing severe disease”. Nature 591 (7851): 513-514. Bibcode: 2021Natur.591..513L. doi:10.1038/d41586-021-00650-7. PMID 33712752.
Pinto D, Park YJ, Beltramello M, Walls AC, Tortorici MA, Bianchi S, Jaconi S, Culap K, Zatta F, De Marco A, Peter A, Guarino B, Spreafico R, Cameroni E, Case JB, Chen RE, Havenar-Daughton C, Snell G, Telenti A, Virgin HW, Lanzavecchia A, Diamond MS, Fink K, Veesler D, Corti D (July 2020). “Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody”. Nature 583 (7815): 290-295. Bibcode: 2020Natur.583..290P. doi:10.1038/s41586-020-2349-y. PMID 32422645.

nih.gov

pubmed.ncbi.nlm.nih.gov

Ledford H (March 2021). “COVID antibody treatments show promise for preventing severe disease”. Nature 591 (7851): 513-514. Bibcode: 2021Natur.591..513L. doi:10.1038/d41586-021-00650-7. PMID 33712752.
Pinto D, Park YJ, Beltramello M, Walls AC, Tortorici MA, Bianchi S, Jaconi S, Culap K, Zatta F, De Marco A, Peter A, Guarino B, Spreafico R, Cameroni E, Case JB, Chen RE, Havenar-Daughton C, Snell G, Telenti A, Virgin HW, Lanzavecchia A, Diamond MS, Fink K, Veesler D, Corti D (July 2020). “Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody”. Nature 583 (7815): 290-295. Bibcode: 2020Natur.583..290P. doi:10.1038/s41586-020-2349-y. PMID 32422645.
Saunders KO (2019). “Conceptual Approaches to Modulating Antibody Effector Functions and Circulation Half-Life” (English). Frontiers in Immunology 10: 1296. doi:10.3389/fimmu.2019.01296. PMC 6568213. PMID 31231397.

pmda.go.jp

info.pmda.go.jp

“ゼビュディ点滴静注液500mg 添付文書”. www.info.pmda.go.jp. 2021年11月1日閲覧。

tga.gov.au

“Xevudy”. Therapeutic Goods Administration (TGA) (20 August 2021). 17 September 2021閲覧。
"TGA provisionally approves GlaxoSmithKline's COVID-19 treatment: sotrovimab (Xevudy)". Therapeutic Goods Administration (TGA) (Press release). 20 August 2021. 2021年9月4日閲覧。
“COVID-19 treatment: GlaxoSmithKline Australia Pty Ltd, sotrovimab (Xevudy)”. Therapeutic Goods Administration (TGA) (20 August 2021). 22 October 2021閲覧。