Ibrutinib (English Wikipedia)
Analysis of information sources in references of the Wikipedia article "Ibrutinib" in English language version.
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abbvie.com
news.abbvie.com
- "Imbruvica (ibrutinib) Now Approved to Treat Waldenstrom's Macroglobulinemia in Europe". AbbVie. 10 July 2015. Archived from the original on 13 July 2020. Retrieved 21 April 2020.
- "Imbruvica (ibrutinib) Approved by U.S. FDA for the First-line Treatment of Chronic Lymphocytic Leukemia". AbbVie (Press release). 4 March 2016. Archived from the original on 22 April 2020. Retrieved 21 April 2020.
- "U.S. FDA Expands Imbruvica (ibrutinib) Label to Include Overall Survival Data in Previously Untreated Chronic Lymphocytic Leukemia (CLL) and New Indication for Small Lymphocytic Lymphoma (SLL) Patients". AbbVie (Press release). 9 May 2016. Archived from the original on 22 April 2020. Retrieved 21 April 2020.
- "U.S. FDA Approves Imbruvica (ibrutinib) as First Treatment Specifically Indicated for Relapsed/Refractory Marginal Zone Lymphoma (MZL) - a Rare Type of Non-Hodgkin's Lymphoma". AbbVie (Press release). 19 January 2017. Retrieved 21 April 2020.
- "U.S. FDA Approves Imbruvica (ibrutinib) as First Approved Treatment Specifically for Adults with Chronic Graft-Versus-Host-Disease (cGVHD) -- A Serious, Potentially Life-Threatening Condition -- After Failure of One or More Lines of Systemic Therapy". AbbVie (Press release). 2 August 2017. Retrieved 21 April 2020.
- "AbbVie Announces Imbruvica (ibrutinib) Plus Rituximab Approval by U.S. FDA as First Chemotherapy-Free Combination Treatment in Adults with Waldenström's Macroglobulinemia, a Rare Type of Blood Cancer". AbbVie (Press release). 27 August 2018. Retrieved 21 April 2020.
- "AbbVie Announces U.S. FDA Approval of Imbruvica (ibrutinib) Plus Obinutuzumab (GAZYVA) - First Chemotherapy-Free, Anti-CD20 Combination Regimen Approved for Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL) in Previously Untreated Patients". AbbVie (Press release). 28 January 2019. Retrieved 21 April 2020.
ajmc.com
- "CMS Releases List of 10 Drugs Subject to Price Negotiation Under IRA". AJMC. 29 August 2023. Retrieved 17 March 2024.
bloomberg.com
- Langreth R, Coffey B (26 February 2015). "Cancer Drug Once Bought for $7 Million May Now Fetch $18 Billion". Bloomberg.com.
cancernetwork.com
- Azvolinsky A. "FDA Approves Ibrutinib for Chronic Lymphocytic Leukemia". Cancer Network. Archived from the original on 22 February 2014. Retrieved 14 February 2014.
chicagotribune.com
- Sachdev A (26 May 2015). "AbbVie closes $21 billion deal for Pharmacyclics". Chicago Tribune.
doi.org
- Xiao L, Salem JE, Clauss S, Hanley A, Bapat A, Hulsmans M, et al. (December 2020). "Ibrutinib-Mediated Atrial Fibrillation Attributable to Inhibition of C-Terminal Src Kinase". Circulation. 142 (25): 2443–2455. doi:10.1161/CIRCULATIONAHA.120.049210. PMC 9661397. PMID 33092403.
- Kaur V, Mehta P, Johnsurd J, Govindarajan R (November 2014). "Ibrutinib-associated tumor lysis syndrome in a patient with chronic lymphocytic leukemia". Blood. 124 (23): 3503–3505. doi:10.1182/blood-2014-08-591875. PMID 25431479.
- de Vries R, Smit JW, Hellemans P, Jiao J, Murphy J, Skee D, et al. (February 2016). "Stable isotope-labelled intravenous microdose for absolute bioavailability and effect of grapefruit juice on ibrutinib in healthy adults". British Journal of Clinical Pharmacology. 81 (2): 235–245. doi:10.1111/bcp.12787. PMC 4833163. PMID 26382728.
- Brown JR (March 2013). "Ibrutinib (PCI-32765), the first BTK (Bruton's tyrosine kinase) inhibitor in clinical trials". Current Hematologic Malignancy Reports. 8 (1): 1–6. doi:10.1007/s11899-012-0147-9. PMC 3584329. PMID 23296407.
- Pavlasova G, Borsky M, Seda V, Cerna K, Osickova J, Doubek M, et al. (September 2016). "Ibrutinib inhibits CD20 upregulation on CLL B cells mediated by the CXCR4/SDF-1 axis". Blood. 128 (12): 1609–1613. doi:10.1182/blood-2016-04-709519. PMC 5291297. PMID 27480113.
- Ponader S, Chen SS, Buggy JJ, Balakrishnan K, Gandhi V, Wierda WG, et al. (February 2012). "The Bruton tyrosine kinase inhibitor PCI-32765 thwarts chronic lymphocytic leukemia cell survival and tissue homing in vitro and in vivo". Blood. 119 (5): 1182–1189. doi:10.1182/blood-2011-10-386417. PMC 4916557. PMID 22180443.
- de Rooij MF, Kuil A, Geest CR, Eldering E, Chang BY, Buggy JJ, et al. (March 2012). "The clinically active BTK inhibitor PCI-32765 targets B-cell receptor- and chemokine-controlled adhesion and migration in chronic lymphocytic leukemia". Blood. 119 (11): 2590–2594. doi:10.1182/blood-2011-11-390989. PMID 22279054.
- Sheridan C (March 2012). "Companies in rapid pursuit of Btk immunokinase". Nature Biotechnology. 30 (3): 199–200. doi:10.1038/nbt0312-199. PMID 22398595. S2CID 205266502.
drugs.com
- "Ibrutinib (Imbruvica) Use During Pregnancy". Drugs.com. 3 December 2019. Retrieved 28 March 2020.
europa.eu
ema.europa.eu
- "Imbruvica EPAR". European Medicines Agency (EMA). 8 July 2021. Retrieved 14 July 2021.
fda.gov
fda.gov
- "FDA approves Imbruvica for rare blood cancer". U.S. Food and Drug Administration (FDA) (Press release). 13 November 2013. Archived from the original on 13 November 2013.
This article incorporates text from this source, which is in the public domain. - "FDA expands approved use of Imbruvica for rare form of non-Hodgkin lymphoma" (Press release). U.S. Food and Drug Administration (FDA). 29 January 2015. Archived from the original on 1 February 2015. This article incorporates text from this source, which is in the public domain.
- "FDA approves treatment for chronic graft versus host disease" (Press release). U.S. Food and Drug Administration (FDA). 2 August 2017. Retrieved 28 March 2020. This article incorporates text from this source, which is in the public domain.
- "FDA expands ibrutinib indications to chronic GVHD". U.S. Food and Drug Administration (FDA). 2 August 2017. Retrieved 21 April 2020.
- "FDA approves ibrutinib for pediatric patients with chronic graft versus host disease, including a new oral suspension". U.S. Food and Drug Administration (FDA). 24 August 2022. Retrieved 24 August 2022.
- "FDA approves ibrutinib plus rituximab for chronic lymphocytic leukemia". U.S. Food and Drug Administration (FDA). 21 April 2020. Retrieved 21 April 2020. This article incorporates text from this source, which is in the public domain.
accessdata.fda.gov
- "Imbruvica (ibrutinib) Capsules". U.S. Food and Drug Administration (FDA). 8 April 2015. Retrieved 21 April 2020.
- "Drug Approval Package: Imbruvica (ibrutinib)". U.S. Food and Drug Administration (FDA). 26 October 2018. Retrieved 22 April 2020.
forbes.com
- Shaywitz D (5 April 2013). "The Wild Story Behind A Promising Experimental Cancer Drug". Forbes.
foreignaffairs.co.nz
- "MIL-OSI Australia: $250 million investment in life changing cancer medicines – ForeignAffairs.co.nz". Foreignaffairs.co.nz. 16 July 2018. Archived from the original on 20 July 2018. Retrieved 20 July 2018.
handle.net
hdl.handle.net
- World Health Organization (2021). World Health Organization model list of essential medicines: 22nd list (2021). Geneva: World Health Organization. hdl:10665/345533. WHO/MHP/HPS/EML/2021.02.
hpfb-dgpsa.ca
dhpp.hpfb-dgpsa.ca
- "Regulatory Decision Summary for Imbruvica". Drug and Health Products Portal. 4 August 2023. Retrieved 2 April 2024.
medicines.org.uk
- "Imbruvica 140 mg Film-Coated Tablets - Summary of Product Characteristics (SmPC)". (emc). 16 January 2020. Retrieved 28 March 2020.
- "UK Ibrutinib label". UK Electronic Medicines Compendium. 25 August 2016. Archived from the original on 30 July 2019. Retrieved 20 November 2016.
medixocentre.com
- "Cost-effectiveness Ibrutinib [Imbruvica] In India, USA, UK, And Australia – Medixocentre.com". Medixocentre.com. 10 February 2020. Retrieved 15 February 2020.
nih.gov
pubmed.ncbi.nlm.nih.gov
- Xiao L, Salem JE, Clauss S, Hanley A, Bapat A, Hulsmans M, et al. (December 2020). "Ibrutinib-Mediated Atrial Fibrillation Attributable to Inhibition of C-Terminal Src Kinase". Circulation. 142 (25): 2443–2455. doi:10.1161/CIRCULATIONAHA.120.049210. PMC 9661397. PMID 33092403.
- Kaur V, Mehta P, Johnsurd J, Govindarajan R (November 2014). "Ibrutinib-associated tumor lysis syndrome in a patient with chronic lymphocytic leukemia". Blood. 124 (23): 3503–3505. doi:10.1182/blood-2014-08-591875. PMID 25431479.
- de Vries R, Smit JW, Hellemans P, Jiao J, Murphy J, Skee D, et al. (February 2016). "Stable isotope-labelled intravenous microdose for absolute bioavailability and effect of grapefruit juice on ibrutinib in healthy adults". British Journal of Clinical Pharmacology. 81 (2): 235–245. doi:10.1111/bcp.12787. PMC 4833163. PMID 26382728.
- Brown JR (March 2013). "Ibrutinib (PCI-32765), the first BTK (Bruton's tyrosine kinase) inhibitor in clinical trials". Current Hematologic Malignancy Reports. 8 (1): 1–6. doi:10.1007/s11899-012-0147-9. PMC 3584329. PMID 23296407.
- Pavlasova G, Borsky M, Seda V, Cerna K, Osickova J, Doubek M, et al. (September 2016). "Ibrutinib inhibits CD20 upregulation on CLL B cells mediated by the CXCR4/SDF-1 axis". Blood. 128 (12): 1609–1613. doi:10.1182/blood-2016-04-709519. PMC 5291297. PMID 27480113.
- Ponader S, Chen SS, Buggy JJ, Balakrishnan K, Gandhi V, Wierda WG, et al. (February 2012). "The Bruton tyrosine kinase inhibitor PCI-32765 thwarts chronic lymphocytic leukemia cell survival and tissue homing in vitro and in vivo". Blood. 119 (5): 1182–1189. doi:10.1182/blood-2011-10-386417. PMC 4916557. PMID 22180443.
- de Rooij MF, Kuil A, Geest CR, Eldering E, Chang BY, Buggy JJ, et al. (March 2012). "The clinically active BTK inhibitor PCI-32765 targets B-cell receptor- and chemokine-controlled adhesion and migration in chronic lymphocytic leukemia". Blood. 119 (11): 2590–2594. doi:10.1182/blood-2011-11-390989. PMID 22279054.
- Sheridan C (March 2012). "Companies in rapid pursuit of Btk immunokinase". Nature Biotechnology. 30 (3): 199–200. doi:10.1038/nbt0312-199. PMID 22398595. S2CID 205266502.
ncbi.nlm.nih.gov
- Xiao L, Salem JE, Clauss S, Hanley A, Bapat A, Hulsmans M, et al. (December 2020). "Ibrutinib-Mediated Atrial Fibrillation Attributable to Inhibition of C-Terminal Src Kinase". Circulation. 142 (25): 2443–2455. doi:10.1161/CIRCULATIONAHA.120.049210. PMC 9661397. PMID 33092403.
- de Vries R, Smit JW, Hellemans P, Jiao J, Murphy J, Skee D, et al. (February 2016). "Stable isotope-labelled intravenous microdose for absolute bioavailability and effect of grapefruit juice on ibrutinib in healthy adults". British Journal of Clinical Pharmacology. 81 (2): 235–245. doi:10.1111/bcp.12787. PMC 4833163. PMID 26382728.
- Brown JR (March 2013). "Ibrutinib (PCI-32765), the first BTK (Bruton's tyrosine kinase) inhibitor in clinical trials". Current Hematologic Malignancy Reports. 8 (1): 1–6. doi:10.1007/s11899-012-0147-9. PMC 3584329. PMID 23296407.
- Pavlasova G, Borsky M, Seda V, Cerna K, Osickova J, Doubek M, et al. (September 2016). "Ibrutinib inhibits CD20 upregulation on CLL B cells mediated by the CXCR4/SDF-1 axis". Blood. 128 (12): 1609–1613. doi:10.1182/blood-2016-04-709519. PMC 5291297. PMID 27480113.
- Ponader S, Chen SS, Buggy JJ, Balakrishnan K, Gandhi V, Wierda WG, et al. (February 2012). "The Bruton tyrosine kinase inhibitor PCI-32765 thwarts chronic lymphocytic leukemia cell survival and tissue homing in vitro and in vivo". Blood. 119 (5): 1182–1189. doi:10.1182/blood-2011-10-386417. PMC 4916557. PMID 22180443.
dailymed.nlm.nih.gov
- "Imbruvica- ibrutinib capsule Imbruvica- ibrutinib tablet, film coated". DailyMed. 8 April 2020. Retrieved 21 April 2020.
semanticscholar.org
api.semanticscholar.org
tga.gov.au
- "Prescription medicines: registration of new chemical entities in Australia, 2015". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 10 April 2023.
washingtonpost.com
- Johnson CY (18 April 2018). "Science hinted that cancer patients could take less of a $148,000-a-year drug. Its maker tripled the price of a pill". The Washington Post. Retrieved 19 April 2018.
- Johnson CY (15 May 2018). "After outcry, drugmakers decide not to triple the price of a cancer pill". The Washington Post. Retrieved 13 June 2018.
web.archive.org
- "UK Ibrutinib label". UK Electronic Medicines Compendium. 25 August 2016. Archived from the original on 30 July 2019. Retrieved 20 November 2016.
- "FDA approves Imbruvica for rare blood cancer". U.S. Food and Drug Administration (FDA) (Press release). 13 November 2013. Archived from the original on 13 November 2013. This article incorporates text from this source, which is in the public domain.
- "FDA expands approved use of Imbruvica for rare form of non-Hodgkin lymphoma" (Press release). U.S. Food and Drug Administration (FDA). 29 January 2015. Archived from the original on 1 February 2015. This article incorporates text from this source, which is in the public domain.
- Azvolinsky A. "FDA Approves Ibrutinib for Chronic Lymphocytic Leukemia". Cancer Network. Archived from the original on 22 February 2014. Retrieved 14 February 2014.
- "Imbruvica (ibrutinib) Now Approved to Treat Waldenstrom's Macroglobulinemia in Europe". AbbVie. 10 July 2015. Archived from the original on 13 July 2020. Retrieved 21 April 2020.
- "Imbruvica (ibrutinib) Approved by U.S. FDA for the First-line Treatment of Chronic Lymphocytic Leukemia". AbbVie (Press release). 4 March 2016. Archived from the original on 22 April 2020. Retrieved 21 April 2020.
- "U.S. FDA Expands Imbruvica (ibrutinib) Label to Include Overall Survival Data in Previously Untreated Chronic Lymphocytic Leukemia (CLL) and New Indication for Small Lymphocytic Lymphoma (SLL) Patients". AbbVie (Press release). 9 May 2016. Archived from the original on 22 April 2020. Retrieved 21 April 2020.
- "MIL-OSI Australia: $250 million investment in life changing cancer medicines – ForeignAffairs.co.nz". Foreignaffairs.co.nz. 16 July 2018. Archived from the original on 20 July 2018. Retrieved 20 July 2018.
wsj.com
- Walker J (1 January 2016). "Patients Struggle With High Drug Prices: Out-of-pocket costs for pricey new drugs leave even some insured and relatively affluent patients with hard choices on how to afford them". The Wall Street Journal. Retrieved 31 January 2019.
- Rockoff JD, Loftus P (5 March 2015). "AbbVie to Buy Pharmacyclics in $21 Billion Deal". The Wall Street Journal.