Adalimumab (English Wikipedia)
Analysis of information sources in references of the Wikipedia article "Adalimumab" in English language version.
refsWebsite
Global rank
English rank
1st place
1st place
3,984th place
2,622nd place
11th place
8th place
low place
low place
49th place
47th place
low place
low place
102nd place
76th place
3,912th place
2,496th place
low place
low place
2,614th place
1,549th place
615th place
407th place
1,697th place
1,040th place
low place
low place
3,823rd place
2,387th place
719th place
636th place
5th place
5th place
5,893rd place
3,320th place
low place
low place
2,662nd place
1,839th place
low place
low place
54th place
48th place
518th place
331st place
low place
low place
993rd place
920th place
low place
low place
low place
low place
low place
6,625th place
low place
low place
350th place
206th place
low place
low place
low place
low place
12th place
11th place
low place
low place
low place
low place
low place
low place
low place
low place
low place
low place
30th place
24th place
low place
low place
712th place
526th place
low place
low place
2,275th place
1,288th place
9,177th place
5,024th place
7th place
7th place
aafp.org
- Welch B (15 December 2008). "Adalimumab (Humira) for the Treatment of Rheumatoid Arthritis". American Family Physician. 78 (12): 1406–1408. ISSN 0002-838X. Archived from the original on 24 November 2020. Retrieved 9 September 2019.
abbott.com
- "Five-Year Data Demonstrate Initial Use Of Abbott's Humira (Adalimumab) Plus Methotrexate May Prevent Further Joint Damage In Early Rheumatoid Arthritis Patients" (Press release). Abbott. Archived from the original on 22 March 2010. Retrieved 27 July 2009.
abbottinvestor.com
- "Abbott Completes Separation Of Research-Based Pharmaceuticals Business" (Press release). Abbott Laboratories. Archived from the original on 8 August 2020. Retrieved 9 September 2019.
- "Abbott Laboratories' Investigational Fully Human Anti-Tnf Therapy, D2E7 (Adalimumab), Shows Promise In Reducing The Signs And Symptoms Of Rheumatoid Arthritis" (Press release). 12 November 2001. Archived from the original on 4 December 2019. Retrieved 9 September 2019.
- "Abbott Opens New Biotechnology Manufacturing Facility In Puerto Rico" (Press release). Abbott. 10 April 2007. Archived from the original on 30 May 2009. Retrieved 27 July 2009.
- "Abbott's Humira (adalimumab) Receives FDA Approval For Moderate to Severe Chronic Plaque Psoriasis" (Press release). Abbott Laboratories. 18 January 2008. Archived from the original on 7 August 2020. Retrieved 9 September 2019.
abbvie.com
news.abbvie.com
- "AbbVie Reports Full-Year and Fourth-Quarter 2017 Financial Results". AbbVie (Press release). Archived from the original on 12 April 2018. Retrieved 8 March 2018.
alvotech.com
investors.alvotech.com
- "Alvotech and Bioventure Announce Approval of AVT02 (adalimumab) as Simlandi in Saudi Arabia". Alvotech. 24 January 2023. Archived from the original on 26 February 2024. Retrieved 26 February 2024.
basf.us
www2.basf.us
- "BASF to focus more strongly on innovative chemistry, a highly efficient Verbund and a global presence" (Press release). Archived from the original on 12 February 2013. Retrieved 9 December 2012.
bbc.co.uk
news.bbc.co.uk
- "Biotech firm wins royalty fight". BBC News Online. 20 December 2004. Archived from the original on 27 August 2021. Retrieved 23 April 2010.
biopharma-reporter.com
- Hargreaves B (16 October 2018). "First wave of Humira biosimilars enters EU market". BioPharma-Reporter. Archived from the original on 15 August 2020. Retrieved 26 November 2018.
boehringer-ingelheim.us
- "Boehringer Ingelheim Pharmaceuticals, Inc. receives FDA approval for Cyltezo (adalimumab-adbm), a biosimilar to Humira, for the treatment of multiple chronic inflammatory diseases" (Press release). Boehringer Ingelheim Pharmaceuticals. 29 August 2017. Archived from the original on 24 July 2019. Retrieved 19 March 2019.
business-standard.com
- "Torrent launches world's second biosimilar of generic auto-immune drug". Business Standard. 11 January 2016. Archived from the original on 26 February 2016. Retrieved 1 March 2016.
businessweek.com
- Decker S (23 February 2011). "Abbott Wins Reversal of J&J's $1.67 Billion Patent Victory". Bloomberg Businessweek. Archived from the original on 6 May 2011.
businesswire.com
- "JAMP and Alvotech Announce Canadian Approval of Simlandi, a High-Concentration Biosimilar to Humira, Providing Access to Previously Unavailable Versions in Canada" (Press release). Alvotech. 10 January 2022. Archived from the original on 26 February 2024. Retrieved 26 February 2024 – via Business Wire.
- "Celltrion USA Announces U.S. FDA Approval of Yuflyma (adalimumab-aaty), a High-Concentration and Citrate-Free Formulation of Humira (adalimumab) Biosimilar" (Press release). Celltrion. 24 May 2023. Archived from the original on 25 May 2023. Retrieved 28 May 2023 – via Business Wire.
cadilapharma.com
- "Cadila Pharmaceuticals launches Cadalimab (Adalimumab biosimilar) for India". Cadila Pharmaceuticals (Press release). 28 August 2020. Archived from the original on 30 November 2022. Retrieved 11 February 2023.
cambridgenetwork.co.uk
- "Cambridge Antibody Technology prevails in High Court proceedings regarding Humira". www.cambridgenetwork.co.uk. Cambridge Network. 20 December 2004. Archived from the original on 9 January 2021. Retrieved 5 January 2021.
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.
clincalc.com
- "The Top 300 of 2021". ClinCalc. Archived from the original on 15 January 2024. Retrieved 14 January 2024.
- "Adalimumab - Drug Usage Statistics". ClinCalc. Archived from the original on 8 July 2020. Retrieved 14 January 2024.
dddmag.com
- "Humira Lifts AbbVie 2.8% in Q2". Discovery and Development. Associated Press. 25 July 2014. Archived from the original on 27 July 2014. Retrieved 27 July 2014.
doi.org
- Peyrin-Biroulet L, Danese S, Cummings F, Atreya R, Greveson K, Pieper B, et al. (August 2019). "Anti-TNF biosimilars in Crohn's Disease: a patient-centric interdisciplinary approach". Expert Review of Gastroenterology & Hepatology. 13 (8): 731–738. doi:10.1080/17474124.2019.1645595. PMID 31322440.
- Navarro-Sarabia F, Ariza-Ariza R, Hernandez-Cruz B, Villanueva I (July 2005). "Adalimumab for treating rheumatoid arthritis". The Cochrane Database of Systematic Reviews (3): CD005113. doi:10.1002/14651858.CD005113.pub2. PMID 16034967.
- Brunner HI, Nanda K, Toth M, Foeldvari I, Bohnsack J, Milojevic D, et al. (October 2020). "Safety and Effectiveness of Adalimumab in Patients With Polyarticular Course of Juvenile Idiopathic Arthritis: STRIVE Registry Seven-Year Interim Results". Arthritis Care & Research. 72 (10): 1420–1430. doi:10.1002/acr.24044. PMC 7589221. PMID 31421019.
- Horneff G, Seyger MM, Arikan D, Kalabic J, Anderson JK, Lazar A, et al. (October 2018). "Safety of Adalimumab in Pediatric Patients with Polyarticular Juvenile Idiopathic Arthritis, Enthesitis-Related Arthritis, Psoriasis, and Crohn's Disease". The Journal of Pediatrics. 201: 166–175.e3. doi:10.1016/j.jpeds.2018.05.042. hdl:2066/195625. PMID 30054164.
- Correll CK, Bullock DR, Cafferty RM, Vehe RK (February 2018). "Safety of weekly adalimumab in the treatment of juvenile idiopathic arthritis and pediatric chronic uveitis". Clinical Rheumatology. 37 (2): 549–553. doi:10.1007/s10067-017-3890-4. PMID 29103180. S2CID 20099281.
- Maxwell LJ, Zochling J, Boonen A, Singh JA, Veras MM, Tanjong Ghogomu E, et al. (April 2015). "TNF-alpha inhibitors for ankylosing spondylitis" (PDF). The Cochrane Database of Systematic Reviews. 2015 (4): CD005468. doi:10.1002/14651858.CD005468.pub2. PMC 11200207. PMID 25887212. Archived (PDF) from the original on 30 April 2024. Retrieved 14 December 2019.
- Podolsky DK (August 2002). "Inflammatory bowel disease" (PDF). The New England Journal of Medicine. 347 (6): 417–429. doi:10.1056/NEJMra020831. PMID 12167685. Archived from the original on 14 March 2020. Retrieved 24 September 2019.
{{cite journal}}: CS1 maint: unfit URL (link) - Gearry RB, Frampton C, Inns S, Poppelwell D, Rademaker M, Suppiah R (October 2019). "VITALITY: impact of adalimumab on health and disability outcomes in patients with Crohn's disease, rheumatoid arthritis, or psoriasis treated in clinical practice in New Zealand". Current Medical Research and Opinion. 35 (10): 1837–1846. doi:10.1080/03007995.2019.1634952. PMID 31233347. S2CID 195354397.
- Croom KF, McCormack PL (2009). "Adalimumab: in plaque psoriasis". American Journal of Clinical Dermatology. 10 (1): 43–50. doi:10.2165/0128071-200910010-00008. PMID 19170412.
- Menter A, Tyring SK, Gordon K, Kimball AB, Leonardi CL, Langley RG, et al. (January 2008). "Adalimumab therapy for moderate to severe psoriasis: A randomized, controlled phase III trial". Journal of the American Academy of Dermatology. 58 (1): 106–115. doi:10.1016/j.jaad.2007.09.010. PMID 17936411.
- Gulliver W, Zouboulis CC, Prens E, Jemec GB, Tzellos T (September 2016). "Evidence-based approach to the treatment of hidradenitis suppurativa/acne inversa, based on the European guidelines for hidradenitis suppurativa". Reviews in Endocrine & Metabolic Disorders. 17 (3): 343–351. doi:10.1007/s11154-016-9328-5. PMC 5156664. PMID 26831295.
- Maarouf M, Clark AK, Lee DE, Shi VY (August 2018). "Targeted treatments for hidradenitis suppurativa: a review of the current literature and ongoing clinical trials". The Journal of Dermatological Treatment. 29 (5): 441–449. doi:10.1080/09546634.2017.1395806. PMID 29098911. S2CID 39246564.
- Hochman D, Wolff B (November 2006). "Risk of serious infections and malignancies with anti-TNF antibody therapy in rheumatoid arthritis". JAMA. 296 (18): 2203, author reply 2203-2203, author reply 2204. doi:10.1001/jama.296.18.2203-a. PMID 17090763.
- Chen Y, Friedman M, Liu G, Deodhar A, Chu CQ (January 2018). "Do tumor necrosis factor inhibitors increase cancer risk in patients with chronic immune-mediated inflammatory disorders?". Cytokine. 101: 78–88. doi:10.1016/j.cyto.2016.09.013. PMID 27688201. S2CID 20837188.
- Yoshida T, Otaki Y, Katsuyama N, Seki M, Kubota J (November 2019). "New adalimumab formulation associated with less injection site pain and improved motivation for treatment". Modern Rheumatology. 29 (6): 949–953. doi:10.1080/14397595.2018.1520426. PMID 30183438. S2CID 52160836.
- Frenzel A, Schirrmann T, Hust M (October 2016). "Phage display-derived human antibodies in clinical development and therapy". mAbs. 8 (7): 1177–1194. doi:10.1080/19420862.2016.1212149. PMC 5058633. PMID 27416017.
- Brekke OH, Sandlie I (January 2003). "Therapeutic antibodies for human diseases at the dawn of the twenty-first century". Nature Reviews. Drug Discovery. 2 (1): 52–62. doi:10.1038/nrd984. PMID 12509759. S2CID 3181573.
- McCafferty J (2010). "The long and winding road to antibody therapeutics". mAbs. 2 (5): 459–460. doi:10.4161/mabs.2.5.13088. PMC 2958567. PMID 20978369.
- Kempeni J (November 1999). "Preliminary results of early clinical trials with the fully human anti-TNFalpha monoclonal antibody D2E7". Annals of the Rheumatic Diseases. 58 (Suppl 1): I70–I72. doi:10.1136/ard.58.2008.i70. PMC 1766582. PMID 10577977.
- Jespers LS, Roberts A, Mahler SM, Winter G, Hoogenboom HR (September 1994). "Guiding the selection of human antibodies from phage display repertoires to a single epitope of an antigen". Bio/Technology. 12 (9): 899–903. doi:10.1038/nbt0994-899. PMID 7521646. S2CID 6096492.
- Rau R (November 2002). "Adalimumab (a fully human anti-tumour necrosis factor alpha monoclonal antibody) in the treatment of active rheumatoid arthritis: the initial results of five trials". Annals of the Rheumatic Diseases. 61 (Suppl 2): ii70–ii73. doi:10.1136/ard.61.suppl_2.ii70. PMC 1766697. PMID 12379628.
- Papagoras C, Voulgari PV, Drosos AA (2009). "Long-term use of adalimumab in the treatment of rheumatic diseases". Open Access Rheumatology: Research and Reviews. 1: 51–68. doi:10.2147/oarrr.s4297. PMC 5074727. PMID 27789981.
- Urquhart L (April 2021). "Top companies and drugs by sales in 2020". Nature Reviews. Drug Discovery. 20 (4): 253. doi:10.1038/d41573-021-00050-6. PMID 33727694. S2CID 232262026.
drugs.com
- "Adalimumab Pregnancy and Breastfeeding Warnings". Drugs.com. Archived from the original on 17 April 2021. Retrieved 19 March 2019.
- "Adalimumab Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. 14 May 2018. Archived from the original on 21 November 2020. Retrieved 18 March 2019.
england.nhs.uk
- "NHS set to save record £300 million on the NHS's highest drug spend". NHS England. 26 November 2018. Archived from the original on 3 January 2022. Retrieved 3 January 2022.
europa.eu
ema.europa.eu
- "Amgevita EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Amsparity EPAR". European Medicines Agency (EMA). 9 December 2019. Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Cyltezo EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 6 August 2020. Retrieved 18 February 2020.
- "Halimatoz EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Hefiya EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 15 October 2019. Retrieved 18 February 2020.
- "Hukyndra EPAR". European Medicines Agency (EMA). 14 September 2021. Archived from the original on 24 April 2022. Retrieved 23 April 2022.
- "Hulio EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 24 March 2020. Retrieved 18 February 2020.
- "Hyrimoz EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 16 November 2019. Retrieved 18 February 2020.
- "Idacio EPAR". European Medicines Agency (EMA). 29 January 2019. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Imraldi EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 24 March 2020. Retrieved 18 February 2020.
- "Kromeya EPAR". European Medicines Agency (EMA). 29 January 2019. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Libmyris EPAR". European Medicines Agency (EMA). 14 September 2021. Archived from the original on 24 April 2022. Retrieved 23 April 2022.
- "Solymbic EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 25 June 2019. Retrieved 18 February 2020.
- "Trudexa EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 18 February 2020. Retrieved 27 August 2021.
- "Yuflyma EPAR". European Medicines Agency (EMA). 9 December 2020. Archived from the original on 28 August 2021. Retrieved 27 February 2021.
- "Humira EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 18 February 2020. Retrieved 18 February 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- "Trudexa EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 18 February 2020. Retrieved 18 February 2020.
expresspharma.in
- "Cadila Pharma launches Cadalimab (adalimumab biosimilar) for India". Express Pharma. 29 August 2020. Archived from the original on 10 June 2022. Retrieved 7 September 2020.
fda.gov
accessdata.fda.gov
- "Hyrimoz: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). 30 October 2018. Archived from the original on 7 December 2019. Retrieved 6 December 2019.
This article incorporates text from this source, which is in the public domain. - "Drug Approval Package: Humira (adalimumab)". U.S. Food and Drug Administration (FDA). 7 April 2017. Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- Siegel JP (31 December 2002). "Product Approval Information - Licensing Action". U.S. Food and Drug Administration (FDA). Archived from the original on 24 October 2020. Retrieved 4 February 2014. This article incorporates text from this source, which is in the public domain.
- "Humira: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Drug Approval Package: Amjevita (adalimumab-atto)". U.S. Food and Drug Administration (FDA). 9 November 2016. Archived from the original on 4 October 2020. Retrieved 11 February 2020.
- "Amjevita: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Drug Approval Package: Cyltezo (adalimumab-adbm)". U.S. Food and Drug Administration (FDA). 27 September 2018. Archived from the original on 4 October 2020. Retrieved 11 February 2020.
- "Cyltezo: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Drug Approval Package: Hyrimoz". U.S. Food and Drug Administration (FDA). 21 March 2019. Archived from the original on 18 December 2019. Retrieved 11 February 2020.
- "Hadlima: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 8 November 2019. This article incorporates text from this source, which is in the public domain.
- "Drug Approval Package: Hadlima". U.S. Food and Drug Administration (FDA). 5 September 2019. Archived from the original on 18 December 2019. Retrieved 11 February 2020.
- "Abrilada: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). 15 November 2019. Archived from the original on 7 December 2019. Retrieved 6 December 2019.
- "Drug Approval Package: Abrilada". U.S. Food and Drug Administration (FDA). 28 January 2020. Archived from the original on 4 October 2020. Retrieved 11 February 2020.
- "Drug Approval Package: Hulio". U.S. Food and Drug Administration (FDA). 2 October 2020. Archived from the original on 6 November 2021. Retrieved 27 December 2021.
- "Drug Approval Package: Idacio". U.S. Food and Drug Administration (FDA). 9 February 2023. Archived from the original on 10 February 2023. Retrieved 9 February 2023.
- "Drug Approval Package: Yuflyma injection". U.S. Food and Drug Administration (FDA). 11 August 2023. Archived from the original on 25 August 2023. Retrieved 11 March 2024.
fda.gov
- "FDA approves Humira to treat ulcerative colitis" (Press release). U.S. Food and Drug Administration (FDA). 28 September 2012. Archived from the original on 30 September 2012. This article incorporates text from this source, which is in the public domain.
- "Biosimilar Drug Information". U.S. Food and Drug Administration (FDA). 27 December 2021. Archived from the original on 28 August 2021. Retrieved 27 December 2021.
- "FDA approves Amjevita, a biosimilar to Humira" (Press release). U.S. Food and Drug Administration (FDA). 23 September 2016. Archived from the original on 19 November 2019. Retrieved 18 November 2019. This article incorporates text from this source, which is in the public domain.
- "FDA Approves Cyltezo, the First Interchangeable Biosimilar to Humira". U.S. Food and Drug Administration. 18 October 2021. Archived from the original on 21 October 2021. Retrieved 11 February 2023.
- "Statement from Sarah Yim, M.D., acting director of the Office of Therapeutic Biologics and Biosimilars in the FDA's Center for Drug Evaluation and Research, on FDA's continued progress facilitating competition in the biologic marketplace with approval of 25th biosimilar product". U.S. Food and Drug Administration (FDA). 15 November 2019. Archived from the original on 19 November 2019. Retrieved 18 November 2019. This article incorporates text from this source, which is in the public domain.
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.
figshare.com
- Maxwell LJ, Zochling J, Boonen A, Singh JA, Veras MM, Tanjong Ghogomu E, et al. (April 2015). "TNF-alpha inhibitors for ankylosing spondylitis" (PDF). The Cochrane Database of Systematic Reviews. 2015 (4): CD005468. doi:10.1002/14651858.CD005468.pub2. PMC 11200207. PMID 25887212. Archived (PDF) from the original on 30 April 2024. Retrieved 14 December 2019.
forbes.com
- Japsen B (26 February 2019). "Why Abbvie May Have A Tough Time Defending Humira's Price Before Congress". Forbes. Archived from the original on 27 February 2019. Retrieved 9 September 2019.
genengnews.com
- Philippidis A (6 March 2017). "The Top 15 Best-Selling Drugs of 2016". Genengnews.com. Archived from the original on 8 March 2018. Retrieved 8 March 2018.
globenewswire.com
- "Coherus Announces U.S. FDA Approval of Yusimry (adalimumab-aqvh)". Coherus BioSciences (Press release). 20 December 2021. Archived from the original on 28 December 2021. Retrieved 27 December 2021 – via GlobeNewswire.
- "Alvotech and Teva Announce U.S. Approval of Simlandi (adalimumab-ryvk) injection, the first interchangeable high-concentration, citrate-free biosimilar to Humira" (Press release). Alvotech. 24 February 2024. Archived from the original on 26 February 2024. Retrieved 26 February 2024 – via GlobeNewswire.
handle.net
hdl.handle.net
- World Health Organization (2023). The selection and use of essential medicines 2023: web annex A: World Health Organization model list of essential medicines: 23rd list (2023). Geneva: World Health Organization. hdl:10665/371090. WHO/MHP/HPS/EML/2023.02.
- Horneff G, Seyger MM, Arikan D, Kalabic J, Anderson JK, Lazar A, et al. (October 2018). "Safety of Adalimumab in Pediatric Patients with Polyarticular Juvenile Idiopathic Arthritis, Enthesitis-Related Arthritis, Psoriasis, and Crohn's Disease". The Journal of Pediatrics. 201: 166–175.e3. doi:10.1016/j.jpeds.2018.05.042. hdl:2066/195625. PMID 30054164.
hres.ca
hpr-rps.hres.ca
- "Summary Basis of Decision (SBD) for Abrilada". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Simlandi". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Idacio". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Amgevita". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Hulio". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Hyrimoz". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Yuflyma". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
markmanadvisors.com
- Silbersher Z (10 June 2020). "Why was the Humira "patent thicket" antitrust case against AbbVie dismissed?". Markman Advisors. Archived from the original on 20 September 2020. Retrieved 6 October 2020.
mediaroom.com
abbott.mediaroom.com
- "Abbott's Humira (adalimumab) Receives U.S. FDA Approval for the Treatment of Adult Patients with Moderate to Severe Ulcerative Colitis". Abbott (Press release). 28 September 2012. Archived from the original on 19 November 2019. Retrieved 18 November 2019.
medicines.org.uk
- "Humira 40 mg solution for injection in pre-filled syringe - Summary of Product Characteristics (SmPC)". (emc). 27 November 2019. Archived from the original on 4 August 2020. Retrieved 12 August 2020.
medscape.com
- Megan B (11 September 2015). "FDA Clears Adalimumab (Humira) for Hidradenitis Suppurativa". Medscape. Archived from the original on 21 January 2021. Retrieved 13 October 2017.
mrctechnology.org
- "Multi-Million Dollar Deal To Benefit Medical Research" (PDF) (Press release). Medical Research Council. Archived from the original (PDF) on 27 June 2007. Retrieved 20 July 2009.
natlawreview.com
- Hansen K, Kolinsky MA (17 February 2020). "Humira: How far can drug makers go to protect their branded market?". The National Law Review. Archived from the original on 21 January 2022. Retrieved 28 January 2023.
nhs.uk
- "Adalimumab (Humira) and its biosimilars: medicine used for joint pain and inflammation". NHS (UK). 18 February 2019. Archived from the original on 3 January 2022. Retrieved 3 January 2022.
nih.gov
pubmed.ncbi.nlm.nih.gov
- Peyrin-Biroulet L, Danese S, Cummings F, Atreya R, Greveson K, Pieper B, et al. (August 2019). "Anti-TNF biosimilars in Crohn's Disease: a patient-centric interdisciplinary approach". Expert Review of Gastroenterology & Hepatology. 13 (8): 731–738. doi:10.1080/17474124.2019.1645595. PMID 31322440.
- Navarro-Sarabia F, Ariza-Ariza R, Hernandez-Cruz B, Villanueva I (July 2005). "Adalimumab for treating rheumatoid arthritis". The Cochrane Database of Systematic Reviews (3): CD005113. doi:10.1002/14651858.CD005113.pub2. PMID 16034967.
- Brunner HI, Nanda K, Toth M, Foeldvari I, Bohnsack J, Milojevic D, et al. (October 2020). "Safety and Effectiveness of Adalimumab in Patients With Polyarticular Course of Juvenile Idiopathic Arthritis: STRIVE Registry Seven-Year Interim Results". Arthritis Care & Research. 72 (10): 1420–1430. doi:10.1002/acr.24044. PMC 7589221. PMID 31421019.
- Horneff G, Seyger MM, Arikan D, Kalabic J, Anderson JK, Lazar A, et al. (October 2018). "Safety of Adalimumab in Pediatric Patients with Polyarticular Juvenile Idiopathic Arthritis, Enthesitis-Related Arthritis, Psoriasis, and Crohn's Disease". The Journal of Pediatrics. 201: 166–175.e3. doi:10.1016/j.jpeds.2018.05.042. hdl:2066/195625. PMID 30054164.
- Correll CK, Bullock DR, Cafferty RM, Vehe RK (February 2018). "Safety of weekly adalimumab in the treatment of juvenile idiopathic arthritis and pediatric chronic uveitis". Clinical Rheumatology. 37 (2): 549–553. doi:10.1007/s10067-017-3890-4. PMID 29103180. S2CID 20099281.
- Maxwell LJ, Zochling J, Boonen A, Singh JA, Veras MM, Tanjong Ghogomu E, et al. (April 2015). "TNF-alpha inhibitors for ankylosing spondylitis" (PDF). The Cochrane Database of Systematic Reviews. 2015 (4): CD005468. doi:10.1002/14651858.CD005468.pub2. PMC 11200207. PMID 25887212. Archived (PDF) from the original on 30 April 2024. Retrieved 14 December 2019.
- Podolsky DK (August 2002). "Inflammatory bowel disease" (PDF). The New England Journal of Medicine. 347 (6): 417–429. doi:10.1056/NEJMra020831. PMID 12167685. Archived from the original on 14 March 2020. Retrieved 24 September 2019.
{{cite journal}}: CS1 maint: unfit URL (link) - Gearry RB, Frampton C, Inns S, Poppelwell D, Rademaker M, Suppiah R (October 2019). "VITALITY: impact of adalimumab on health and disability outcomes in patients with Crohn's disease, rheumatoid arthritis, or psoriasis treated in clinical practice in New Zealand". Current Medical Research and Opinion. 35 (10): 1837–1846. doi:10.1080/03007995.2019.1634952. PMID 31233347. S2CID 195354397.
- Croom KF, McCormack PL (2009). "Adalimumab: in plaque psoriasis". American Journal of Clinical Dermatology. 10 (1): 43–50. doi:10.2165/0128071-200910010-00008. PMID 19170412.
- Menter A, Tyring SK, Gordon K, Kimball AB, Leonardi CL, Langley RG, et al. (January 2008). "Adalimumab therapy for moderate to severe psoriasis: A randomized, controlled phase III trial". Journal of the American Academy of Dermatology. 58 (1): 106–115. doi:10.1016/j.jaad.2007.09.010. PMID 17936411.
- Gulliver W, Zouboulis CC, Prens E, Jemec GB, Tzellos T (September 2016). "Evidence-based approach to the treatment of hidradenitis suppurativa/acne inversa, based on the European guidelines for hidradenitis suppurativa". Reviews in Endocrine & Metabolic Disorders. 17 (3): 343–351. doi:10.1007/s11154-016-9328-5. PMC 5156664. PMID 26831295.
- Maarouf M, Clark AK, Lee DE, Shi VY (August 2018). "Targeted treatments for hidradenitis suppurativa: a review of the current literature and ongoing clinical trials". The Journal of Dermatological Treatment. 29 (5): 441–449. doi:10.1080/09546634.2017.1395806. PMID 29098911. S2CID 39246564.
- Hochman D, Wolff B (November 2006). "Risk of serious infections and malignancies with anti-TNF antibody therapy in rheumatoid arthritis". JAMA. 296 (18): 2203, author reply 2203-2203, author reply 2204. doi:10.1001/jama.296.18.2203-a. PMID 17090763.
- Chen Y, Friedman M, Liu G, Deodhar A, Chu CQ (January 2018). "Do tumor necrosis factor inhibitors increase cancer risk in patients with chronic immune-mediated inflammatory disorders?". Cytokine. 101: 78–88. doi:10.1016/j.cyto.2016.09.013. PMID 27688201. S2CID 20837188.
- Yoshida T, Otaki Y, Katsuyama N, Seki M, Kubota J (November 2019). "New adalimumab formulation associated with less injection site pain and improved motivation for treatment". Modern Rheumatology. 29 (6): 949–953. doi:10.1080/14397595.2018.1520426. PMID 30183438. S2CID 52160836.
- Frenzel A, Schirrmann T, Hust M (October 2016). "Phage display-derived human antibodies in clinical development and therapy". mAbs. 8 (7): 1177–1194. doi:10.1080/19420862.2016.1212149. PMC 5058633. PMID 27416017.
- Brekke OH, Sandlie I (January 2003). "Therapeutic antibodies for human diseases at the dawn of the twenty-first century". Nature Reviews. Drug Discovery. 2 (1): 52–62. doi:10.1038/nrd984. PMID 12509759. S2CID 3181573.
- McCafferty J (2010). "The long and winding road to antibody therapeutics". mAbs. 2 (5): 459–460. doi:10.4161/mabs.2.5.13088. PMC 2958567. PMID 20978369.
- Kempeni J (November 1999). "Preliminary results of early clinical trials with the fully human anti-TNFalpha monoclonal antibody D2E7". Annals of the Rheumatic Diseases. 58 (Suppl 1): I70–I72. doi:10.1136/ard.58.2008.i70. PMC 1766582. PMID 10577977.
- Jespers LS, Roberts A, Mahler SM, Winter G, Hoogenboom HR (September 1994). "Guiding the selection of human antibodies from phage display repertoires to a single epitope of an antigen". Bio/Technology. 12 (9): 899–903. doi:10.1038/nbt0994-899. PMID 7521646. S2CID 6096492.
- Rau R (November 2002). "Adalimumab (a fully human anti-tumour necrosis factor alpha monoclonal antibody) in the treatment of active rheumatoid arthritis: the initial results of five trials". Annals of the Rheumatic Diseases. 61 (Suppl 2): ii70–ii73. doi:10.1136/ard.61.suppl_2.ii70. PMC 1766697. PMID 12379628.
- Papagoras C, Voulgari PV, Drosos AA (2009). "Long-term use of adalimumab in the treatment of rheumatic diseases". Open Access Rheumatology: Research and Reviews. 1: 51–68. doi:10.2147/oarrr.s4297. PMC 5074727. PMID 27789981.
- Urquhart L (April 2021). "Top companies and drugs by sales in 2020". Nature Reviews. Drug Discovery. 20 (4): 253. doi:10.1038/d41573-021-00050-6. PMID 33727694. S2CID 232262026.
dailymed.nlm.nih.gov
- "Idacio- adalimumab injection, solution". DailyMed. 22 March 2023. Archived from the original on 11 March 2024. Retrieved 11 March 2024.
- "Yuflyma- adalimumab injection". DailyMed. 27 May 2023. Archived from the original on 26 June 2023. Retrieved 25 June 2023.
- "CYLTEZO- adalimumab-adbm kit". DailyMed. 12 July 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Abrilada- adalimumab-afzb kit; Abrilada- adalimumab-afzb injection, solution". DailyMed. 26 January 2024. Archived from the original on 30 April 2024. Retrieved 11 March 2024.
- "Yusimry- adalimumab-aqvh injection, solution". DailyMed. 31 March 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Amjevita- adalimumab-atto injection". DailyMed. 11 April 2023. Archived from the original on 26 June 2023. Retrieved 25 June 2023.
- "Hadlima- adalimumab-bwwd solution". DailyMed. 11 July 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Hulio- adalimumab kit". DailyMed. 9 August 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Simlandi- adalimumab-ryvk kit". DailyMed. 23 February 2024. Archived from the original on 2 April 2024. Retrieved 2 April 2024.
- "Humira- adalimumab kit Humira- adalimumab injection, solution". DailyMed. Archived from the original on 21 June 2020. Retrieved 18 February 2020.
- "Imraldi- adalimumab injection, solution". DailyMed. 23 January 2018. Archived from the original on 21 September 2020. Retrieved 18 February 2020.
- "Remicade- infliximab injection, powder, lyophilized, for solution". DailyMed. 8 April 2022. Retrieved 22 May 2024.
- "Enbrel- etanercept solution Enbrel- etanercept kit". DailyMed. Retrieved 17 April 2021.
- "Amjevita- adalimumab-atto injection". DailyMed. 11 April 2023. Archived from the original on 26 June 2023. Retrieved 25 June 2023.
- "Abrilada- adalimumab-afzb kit; Abrilada- adalimumab-afzb solution". DailyMed. 26 January 2024. Archived from the original on 30 April 2024. Retrieved 11 March 2024.
ncbi.nlm.nih.gov
- Brunner HI, Nanda K, Toth M, Foeldvari I, Bohnsack J, Milojevic D, et al. (October 2020). "Safety and Effectiveness of Adalimumab in Patients With Polyarticular Course of Juvenile Idiopathic Arthritis: STRIVE Registry Seven-Year Interim Results". Arthritis Care & Research. 72 (10): 1420–1430. doi:10.1002/acr.24044. PMC 7589221. PMID 31421019.
- Maxwell LJ, Zochling J, Boonen A, Singh JA, Veras MM, Tanjong Ghogomu E, et al. (April 2015). "TNF-alpha inhibitors for ankylosing spondylitis" (PDF). The Cochrane Database of Systematic Reviews. 2015 (4): CD005468. doi:10.1002/14651858.CD005468.pub2. PMC 11200207. PMID 25887212. Archived (PDF) from the original on 30 April 2024. Retrieved 14 December 2019.
- Gulliver W, Zouboulis CC, Prens E, Jemec GB, Tzellos T (September 2016). "Evidence-based approach to the treatment of hidradenitis suppurativa/acne inversa, based on the European guidelines for hidradenitis suppurativa". Reviews in Endocrine & Metabolic Disorders. 17 (3): 343–351. doi:10.1007/s11154-016-9328-5. PMC 5156664. PMID 26831295.
- Frenzel A, Schirrmann T, Hust M (October 2016). "Phage display-derived human antibodies in clinical development and therapy". mAbs. 8 (7): 1177–1194. doi:10.1080/19420862.2016.1212149. PMC 5058633. PMID 27416017.
- McCafferty J (2010). "The long and winding road to antibody therapeutics". mAbs. 2 (5): 459–460. doi:10.4161/mabs.2.5.13088. PMC 2958567. PMID 20978369.
- Kempeni J (November 1999). "Preliminary results of early clinical trials with the fully human anti-TNFalpha monoclonal antibody D2E7". Annals of the Rheumatic Diseases. 58 (Suppl 1): I70–I72. doi:10.1136/ard.58.2008.i70. PMC 1766582. PMID 10577977.
- Rau R (November 2002). "Adalimumab (a fully human anti-tumour necrosis factor alpha monoclonal antibody) in the treatment of active rheumatoid arthritis: the initial results of five trials". Annals of the Rheumatic Diseases. 61 (Suppl 2): ii70–ii73. doi:10.1136/ard.61.suppl_2.ii70. PMC 1766697. PMID 12379628.
- Papagoras C, Voulgari PV, Drosos AA (2009). "Long-term use of adalimumab in the treatment of rheumatic diseases". Open Access Rheumatology: Research and Reviews. 1: 51–68. doi:10.2147/oarrr.s4297. PMC 5074727. PMID 27789981.
nytimes.com
- Rebecca R (28 January 2023). "How a Drug Company Made $114 Billion by Gaming the US Patent System". The New York Times. Archived from the original on 28 January 2023. Retrieved 28 January 2023.
pharmaceutical-journal.com
- Dent E (18 October 2018). "Most expensive NHS drug comes off patent". Pharmaceutical Journal. Archived from the original on 18 May 2021. Retrieved 29 November 2018.
pharmaceutical-technology.com
- Turner S (5 September 2018). "Humira: the highs and lows of the world's most successful drug". Pharmaceutical Technology. Archived from the original on 9 September 2019. Retrieved 9 September 2019.
pharmaphorum.com
- "So it begins: next Humira biosimilars launch in US". pharmaphorum. 4 July 2023. Archived from the original on 5 July 2023. Retrieved 4 July 2023.
pmlive.com
- "First biosimilar Humira launches in India". 17 December 2014. Archived from the original on 25 March 2023. Retrieved 4 July 2023.
- "Sandoz's high concentration Hyrimoz formulation recommended for use in EU". PMLive. 30 January 2023. Archived from the original on 31 January 2023. Retrieved 31 January 2023.
reuters.com
- "India's Cadila launches first cheaper copy of world's top-selling drug". Reuters. 9 December 2014. Archived from the original on 27 March 2019. Retrieved 19 March 2019.
- Wingrove P (30 June 2023). "Analysis: New Humira rivals likely to hit US market with small discounts in July". Reuters. Archived from the original on 30 June 2023. Retrieved 4 July 2023.
- Wingrove P (1 July 2023). "Organon, Samsung Bioepis launch copycat for arthritis drug Humira at 85% discount". Reuters. Archived from the original on 1 July 2023. Retrieved 4 July 2023.
- Pierson R, Spicer J (30 June 2009). "Jury returns $1.67 billion drug verdict against Abbott". Reuters. Archived from the original on 2 March 2021. Retrieved 9 September 2019.
scholar.google.com
- Centocor Ortho Biotech, Inc. v. Abbott Lab'ys, 669 F. Supp. 2d 756 (E.D. Tex. 2009) Archived 22 March 2022 at the Wayback Machine, rev'd, 636 F.3d 1341 (Fed. Cir. 2011).
- "Centocor Ortho Biotech v. Abbott Laboratories, 636 F. 3d 1341". United States Court of Appeals for the Federal Circuit. 23 February 2011. Archived from the original on 27 August 2021. Retrieved 9 September 2019 – via Google Scholar.
sciencedaily.com
- "Treating psoriasis to prevent heart attacks and strokes". ScienceDaily. Archived from the original on 20 September 2018. Retrieved 9 March 2018.
semanticscholar.org
api.semanticscholar.org
- Correll CK, Bullock DR, Cafferty RM, Vehe RK (February 2018). "Safety of weekly adalimumab in the treatment of juvenile idiopathic arthritis and pediatric chronic uveitis". Clinical Rheumatology. 37 (2): 549–553. doi:10.1007/s10067-017-3890-4. PMID 29103180. S2CID 20099281.
- Gearry RB, Frampton C, Inns S, Poppelwell D, Rademaker M, Suppiah R (October 2019). "VITALITY: impact of adalimumab on health and disability outcomes in patients with Crohn's disease, rheumatoid arthritis, or psoriasis treated in clinical practice in New Zealand". Current Medical Research and Opinion. 35 (10): 1837–1846. doi:10.1080/03007995.2019.1634952. PMID 31233347. S2CID 195354397.
- Maarouf M, Clark AK, Lee DE, Shi VY (August 2018). "Targeted treatments for hidradenitis suppurativa: a review of the current literature and ongoing clinical trials". The Journal of Dermatological Treatment. 29 (5): 441–449. doi:10.1080/09546634.2017.1395806. PMID 29098911. S2CID 39246564.
- Chen Y, Friedman M, Liu G, Deodhar A, Chu CQ (January 2018). "Do tumor necrosis factor inhibitors increase cancer risk in patients with chronic immune-mediated inflammatory disorders?". Cytokine. 101: 78–88. doi:10.1016/j.cyto.2016.09.013. PMID 27688201. S2CID 20837188.
- Yoshida T, Otaki Y, Katsuyama N, Seki M, Kubota J (November 2019). "New adalimumab formulation associated with less injection site pain and improved motivation for treatment". Modern Rheumatology. 29 (6): 949–953. doi:10.1080/14397595.2018.1520426. PMID 30183438. S2CID 52160836.
- Brekke OH, Sandlie I (January 2003). "Therapeutic antibodies for human diseases at the dawn of the twenty-first century". Nature Reviews. Drug Discovery. 2 (1): 52–62. doi:10.1038/nrd984. PMID 12509759. S2CID 3181573.
- Jespers LS, Roberts A, Mahler SM, Winter G, Hoogenboom HR (September 1994). "Guiding the selection of human antibodies from phage display repertoires to a single epitope of an antigen". Bio/Technology. 12 (9): 899–903. doi:10.1038/nbt0994-899. PMID 7521646. S2CID 6096492.
- Urquhart L (April 2021). "Top companies and drugs by sales in 2020". Nature Reviews. Drug Discovery. 20 (4): 253. doi:10.1038/d41573-021-00050-6. PMID 33727694. S2CID 232262026.
telegraph.co.uk
- Murray-West R (27 October 2005). "Drug maker CAT surges after royalty settlement". The Telegraph. London. Archived from the original on 20 September 2018. Retrieved 23 April 2010.
tga.gov.au
- "Ciptunec/Ardalicip APMDS". Therapeutic Goods Administration (TGA). 27 September 2022. Retrieved 29 September 2022.
- "Yuflyma APMDS". Therapeutic Goods Administration (TGA). 8 April 2022. Archived from the original on 24 April 2022. Retrieved 24 April 2022.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 8 April 2023. Retrieved 6 October 2023.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- https://www.tga.gov.au/resources/auspar/auspar-adalimumab-4 Archived 8 May 2023 at the Wayback Machine >"AusPAR: Adalimumab". Therapeutic Goods Administration (TGA). 23 September 2020. Archived from the original on 27 October 2020. Retrieved 23 September 2020.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
thefreelibrary.com
- "Eisai Submits New Drug Application for Rheumatoid Arthritis Drug Adalimumab (D2E7) in Japan". thefreelibrary.com. Archived from the original on 13 October 2012. Retrieved 27 July 2009.
theguardian.com
- Heal A (26 November 2018). "NHS replaces highest-spend drug with £300m cheaper alternative". The Guardian. Archived from the original on 26 November 2018. Retrieved 26 November 2018.
truecostofhealthcare.org
- "Abbott 2006 Annual Report" (PDF). Abbott. Archived from the original on 13 January 2008. Retrieved 27 July 2009.
- "Abbott 2007 Annual Report" (PDF). Abbott. Archived from the original on 3 May 2009. Retrieved 27 July 2009.
uscourts.gov
media.ca7.uscourts.gov
- Mayor and City of Baltimore, et al. v. AbbVIE Inc., et al. Archived 3 August 2022 at the Wayback Machine, 7th Circuit Court of Appeals (decided 1 August 2022).
web.archive.org
- "Idacio- adalimumab injection, solution". DailyMed. 22 March 2023. Archived from the original on 11 March 2024. Retrieved 11 March 2024.
- "Yuflyma- adalimumab injection". DailyMed. 27 May 2023. Archived from the original on 26 June 2023. Retrieved 25 June 2023.
- "Hyrimoz: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). 30 October 2018. Archived from the original on 7 December 2019. Retrieved 6 December 2019. This article incorporates text from this source, which is in the public domain.
- "CYLTEZO- adalimumab-adbm kit". DailyMed. 12 July 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Abrilada- adalimumab-afzb kit; Abrilada- adalimumab-afzb injection, solution". DailyMed. 26 January 2024. Archived from the original on 30 April 2024. Retrieved 11 March 2024.
- "Yusimry- adalimumab-aqvh injection, solution". DailyMed. 31 March 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Amjevita- adalimumab-atto injection". DailyMed. 11 April 2023. Archived from the original on 26 June 2023. Retrieved 25 June 2023.
- "Hadlima- adalimumab-bwwd solution". DailyMed. 11 July 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Hulio- adalimumab kit". DailyMed. 9 August 2023. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "Simlandi- adalimumab-ryvk kit". DailyMed. 23 February 2024. Archived from the original on 2 April 2024. Retrieved 2 April 2024.
- "Summary Basis of Decision (SBD) for Abrilada". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
- "Amgevita EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Amsparity EPAR". European Medicines Agency (EMA). 9 December 2019. Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Cadila Pharmaceuticals launches Cadalimab (Adalimumab biosimilar) for India". Cadila Pharmaceuticals (Press release). 28 August 2020. Archived from the original on 30 November 2022. Retrieved 11 February 2023.
- "Cyltezo EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 6 August 2020. Retrieved 18 February 2020.
- "First biosimilar Humira launches in India". 17 December 2014. Archived from the original on 25 March 2023. Retrieved 4 July 2023.
- "Halimatoz EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Hefiya EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 15 October 2019. Retrieved 18 February 2020.
- "Hukyndra EPAR". European Medicines Agency (EMA). 14 September 2021. Archived from the original on 24 April 2022. Retrieved 23 April 2022.
- "Hulio EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 24 March 2020. Retrieved 18 February 2020.
- "Hyrimoz EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 16 November 2019. Retrieved 18 February 2020.
- "Idacio EPAR". European Medicines Agency (EMA). 29 January 2019. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Imraldi EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 24 March 2020. Retrieved 18 February 2020.
- "Kromeya EPAR". European Medicines Agency (EMA). 29 January 2019. Archived from the original on 30 December 2019. Retrieved 18 February 2020.
- "Libmyris EPAR". European Medicines Agency (EMA). 14 September 2021. Archived from the original on 24 April 2022. Retrieved 23 April 2022.
- "Summary Basis of Decision (SBD) for Simlandi". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
- "Solymbic EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 25 June 2019. Retrieved 18 February 2020.
- "Trudexa EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 18 February 2020. Retrieved 27 August 2021.
- "Yuflyma EPAR". European Medicines Agency (EMA). 9 December 2020. Archived from the original on 28 August 2021. Retrieved 27 February 2021.
- "Adalimumab Pregnancy and Breastfeeding Warnings". Drugs.com. Archived from the original on 17 April 2021. Retrieved 19 March 2019.
- "Yuflyma APMDS". Therapeutic Goods Administration (TGA). 8 April 2022. Archived from the original on 24 April 2022. Retrieved 24 April 2022.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 8 April 2023. Retrieved 6 October 2023.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- https://www.tga.gov.au/resources/auspar/auspar-adalimumab-4 Archived 8 May 2023 at the Wayback Machine >"AusPAR: Adalimumab". Therapeutic Goods Administration (TGA). 23 September 2020. Archived from the original on 27 October 2020. Retrieved 23 September 2020.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- AusPAR: Adalimumab. Therapeutic Goods Administration (TGA) (Report). September 2020. Archived from the original on 6 October 2023. Retrieved 6 October 2023.
- "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.
- "Humira 40 mg solution for injection in pre-filled syringe - Summary of Product Characteristics (SmPC)". (emc). 27 November 2019. Archived from the original on 4 August 2020. Retrieved 12 August 2020.
- "Humira- adalimumab kit Humira- adalimumab injection, solution". DailyMed. Archived from the original on 21 June 2020. Retrieved 18 February 2020.
- "Humira EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 18 February 2020. Retrieved 18 February 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- "Adalimumab Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. 14 May 2018. Archived from the original on 21 November 2020. Retrieved 18 March 2019.
- Megan B (11 September 2015). "FDA Clears Adalimumab (Humira) for Hidradenitis Suppurativa". Medscape. Archived from the original on 21 January 2021. Retrieved 13 October 2017.
- "Drug Approval Package: Humira (adalimumab)". U.S. Food and Drug Administration (FDA). 7 April 2017. Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "The Top 300 of 2021". ClinCalc. Archived from the original on 15 January 2024. Retrieved 14 January 2024.
- "Adalimumab - Drug Usage Statistics". ClinCalc. Archived from the original on 8 July 2020. Retrieved 14 January 2024.
- "Imraldi- adalimumab injection, solution". DailyMed. 23 January 2018. Archived from the original on 21 September 2020. Retrieved 18 February 2020.
- Siegel JP (31 December 2002). "Product Approval Information - Licensing Action". U.S. Food and Drug Administration (FDA). Archived from the original on 24 October 2020. Retrieved 4 February 2014. This article incorporates text from this source, which is in the public domain.
- Welch B (15 December 2008). "Adalimumab (Humira) for the Treatment of Rheumatoid Arthritis". American Family Physician. 78 (12): 1406–1408. ISSN 0002-838X. Archived from the original on 24 November 2020. Retrieved 9 September 2019.
- Maxwell LJ, Zochling J, Boonen A, Singh JA, Veras MM, Tanjong Ghogomu E, et al. (April 2015). "TNF-alpha inhibitors for ankylosing spondylitis" (PDF). The Cochrane Database of Systematic Reviews. 2015 (4): CD005468. doi:10.1002/14651858.CD005468.pub2. PMC 11200207. PMID 25887212. Archived (PDF) from the original on 30 April 2024. Retrieved 14 December 2019.
- Podolsky DK (August 2002). "Inflammatory bowel disease" (PDF). The New England Journal of Medicine. 347 (6): 417–429. doi:10.1056/NEJMra020831. PMID 12167685. Archived from the original on 14 March 2020. Retrieved 24 September 2019.
{{cite journal}}: CS1 maint: unfit URL (link) - Morey S (17 September 2009). "UK – Summary of NICE Approvals in September 2009". Archived from the original on 20 September 2018. Retrieved 4 February 2014.
- "FDA approves Humira to treat ulcerative colitis" (Press release). U.S. Food and Drug Administration (FDA). 28 September 2012. Archived from the original on 30 September 2012. This article incorporates text from this source, which is in the public domain.
- "Abbott's Humira (adalimumab) Receives U.S. FDA Approval for the Treatment of Adult Patients with Moderate to Severe Ulcerative Colitis". Abbott (Press release). 28 September 2012. Archived from the original on 19 November 2019. Retrieved 18 November 2019.
- "Abbott Completes Separation Of Research-Based Pharmaceuticals Business" (Press release). Abbott Laboratories. Archived from the original on 8 August 2020. Retrieved 9 September 2019.
- Turner S (5 September 2018). "Humira: the highs and lows of the world's most successful drug". Pharmaceutical Technology. Archived from the original on 9 September 2019. Retrieved 9 September 2019.
- Japsen B (26 February 2019). "Why Abbvie May Have A Tough Time Defending Humira's Price Before Congress". Forbes. Archived from the original on 27 February 2019. Retrieved 9 September 2019.
- "BASF to focus more strongly on innovative chemistry, a highly efficient Verbund and a global presence" (Press release). Archived from the original on 12 February 2013. Retrieved 9 December 2012.
- "Humira: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Trudexa EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Abbott Laboratories' Investigational Fully Human Anti-Tnf Therapy, D2E7 (Adalimumab), Shows Promise In Reducing The Signs And Symptoms Of Rheumatoid Arthritis" (Press release). 12 November 2001. Archived from the original on 4 December 2019. Retrieved 9 September 2019.
- "Abbott 2006 Annual Report" (PDF). Abbott. Archived from the original on 13 January 2008. Retrieved 27 July 2009.
- "Eisai Submits New Drug Application for Rheumatoid Arthritis Drug Adalimumab (D2E7) in Japan". thefreelibrary.com. Archived from the original on 13 October 2012. Retrieved 27 July 2009.
- "Abbott 2007 Annual Report" (PDF). Abbott. Archived from the original on 3 May 2009. Retrieved 27 July 2009.
- "Abbott Opens New Biotechnology Manufacturing Facility In Puerto Rico" (Press release). Abbott. 10 April 2007. Archived from the original on 30 May 2009. Retrieved 27 July 2009.
- "Abbott's Humira (adalimumab) Receives FDA Approval For Moderate to Severe Chronic Plaque Psoriasis" (Press release). Abbott Laboratories. 18 January 2008. Archived from the original on 7 August 2020. Retrieved 9 September 2019.
- "Five-Year Data Demonstrate Initial Use Of Abbott's Humira (Adalimumab) Plus Methotrexate May Prevent Further Joint Damage In Early Rheumatoid Arthritis Patients" (Press release). Abbott. Archived from the original on 22 March 2010. Retrieved 27 July 2009.
- "Treating psoriasis to prevent heart attacks and strokes". ScienceDaily. Archived from the original on 20 September 2018. Retrieved 9 March 2018.
- "Humira Lifts AbbVie 2.8% in Q2". Discovery and Development. Associated Press. 25 July 2014. Archived from the original on 27 July 2014. Retrieved 27 July 2014.
- "India's Cadila launches first cheaper copy of world's top-selling drug". Reuters. 9 December 2014. Archived from the original on 27 March 2019. Retrieved 19 March 2019.
- "Adalimumab (Humira) and its biosimilars: medicine used for joint pain and inflammation". NHS (UK). 18 February 2019. Archived from the original on 3 January 2022. Retrieved 3 January 2022.
- "NHS set to save record £300 million on the NHS's highest drug spend". NHS England. 26 November 2018. Archived from the original on 3 January 2022. Retrieved 3 January 2022.
- Philippidis A (6 March 2017). "The Top 15 Best-Selling Drugs of 2016". Genengnews.com. Archived from the original on 8 March 2018. Retrieved 8 March 2018.
- "AbbVie Reports Full-Year and Fourth-Quarter 2017 Financial Results". AbbVie (Press release). Archived from the original on 12 April 2018. Retrieved 8 March 2018.
- "Torrent launches world's second biosimilar of generic auto-immune drug". Business Standard. 11 January 2016. Archived from the original on 26 February 2016. Retrieved 1 March 2016.
- "Biosimilar Drug Information". U.S. Food and Drug Administration (FDA). 27 December 2021. Archived from the original on 28 August 2021. Retrieved 27 December 2021.
- "Amjevita- adalimumab-atto injection". DailyMed. 11 April 2023. Archived from the original on 26 June 2023. Retrieved 25 June 2023.
- "Drug Approval Package: Amjevita (adalimumab-atto)". U.S. Food and Drug Administration (FDA). 9 November 2016. Archived from the original on 4 October 2020. Retrieved 11 February 2020.
- "FDA approves Amjevita, a biosimilar to Humira" (Press release). U.S. Food and Drug Administration (FDA). 23 September 2016. Archived from the original on 19 November 2019. Retrieved 18 November 2019. This article incorporates text from this source, which is in the public domain.
- "Amjevita: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Drug Approval Package: Cyltezo (adalimumab-adbm)". U.S. Food and Drug Administration (FDA). 27 September 2018. Archived from the original on 4 October 2020. Retrieved 11 February 2020.
- "FDA Approves Cyltezo, the First Interchangeable Biosimilar to Humira". U.S. Food and Drug Administration. 18 October 2021. Archived from the original on 21 October 2021. Retrieved 11 February 2023.
- "Cyltezo: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 18 February 2020. Retrieved 18 February 2020.
- "Boehringer Ingelheim Pharmaceuticals, Inc. receives FDA approval for Cyltezo (adalimumab-adbm), a biosimilar to Humira, for the treatment of multiple chronic inflammatory diseases" (Press release). Boehringer Ingelheim Pharmaceuticals. 29 August 2017. Archived from the original on 24 July 2019. Retrieved 19 March 2019.
- Hargreaves B (16 October 2018). "First wave of Humira biosimilars enters EU market". BioPharma-Reporter. Archived from the original on 15 August 2020. Retrieved 26 November 2018.
- Heal A (26 November 2018). "NHS replaces highest-spend drug with £300m cheaper alternative". The Guardian. Archived from the original on 26 November 2018. Retrieved 26 November 2018.
- Dent E (18 October 2018). "Most expensive NHS drug comes off patent". Pharmaceutical Journal. Archived from the original on 18 May 2021. Retrieved 29 November 2018.
- "Drug Approval Package: Hyrimoz". U.S. Food and Drug Administration (FDA). 21 March 2019. Archived from the original on 18 December 2019. Retrieved 11 February 2020.
- "Hadlima: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 8 November 2019. This article incorporates text from this source, which is in the public domain.
- "Drug Approval Package: Hadlima". U.S. Food and Drug Administration (FDA). 5 September 2019. Archived from the original on 18 December 2019. Retrieved 11 February 2020.
- "Abrilada- adalimumab-afzb kit; Abrilada- adalimumab-afzb solution". DailyMed. 26 January 2024. Archived from the original on 30 April 2024. Retrieved 11 March 2024.
- "Abrilada: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). 15 November 2019. Archived from the original on 7 December 2019. Retrieved 6 December 2019.
- "Drug Approval Package: Abrilada". U.S. Food and Drug Administration (FDA). 28 January 2020. Archived from the original on 4 October 2020. Retrieved 11 February 2020.
- "Statement from Sarah Yim, M.D., acting director of the Office of Therapeutic Biologics and Biosimilars in the FDA's Center for Drug Evaluation and Research, on FDA's continued progress facilitating competition in the biologic marketplace with approval of 25th biosimilar product". U.S. Food and Drug Administration (FDA). 15 November 2019. Archived from the original on 19 November 2019. Retrieved 18 November 2019. This article incorporates text from this source, which is in the public domain.
- "Drug Approval Package: Hulio". U.S. Food and Drug Administration (FDA). 2 October 2020. Archived from the original on 6 November 2021. Retrieved 27 December 2021.
- "Cadila Pharma launches Cadalimab (adalimumab biosimilar) for India". Express Pharma. 29 August 2020. Archived from the original on 10 June 2022. Retrieved 7 September 2020.
- "Summary Basis of Decision (SBD) for Idacio". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Amgevita". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Hulio". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
- "Summary Basis of Decision (SBD) for Hyrimoz". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- "Coherus Announces U.S. FDA Approval of Yusimry (adalimumab-aqvh)". Coherus BioSciences (Press release). 20 December 2021. Archived from the original on 28 December 2021. Retrieved 27 December 2021 – via GlobeNewswire.
- "Summary Basis of Decision (SBD) for Yuflyma". Health Canada. 23 October 2014. Archived from the original on 29 May 2022. Retrieved 29 May 2022.
- "JAMP and Alvotech Announce Canadian Approval of Simlandi, a High-Concentration Biosimilar to Humira, Providing Access to Previously Unavailable Versions in Canada" (Press release). Alvotech. 10 January 2022. Archived from the original on 26 February 2024. Retrieved 26 February 2024 – via Business Wire.
- "Drug Approval Package: Idacio". U.S. Food and Drug Administration (FDA). 9 February 2023. Archived from the original on 10 February 2023. Retrieved 9 February 2023.
- "Sandoz's high concentration Hyrimoz formulation recommended for use in EU". PMLive. 30 January 2023. Archived from the original on 31 January 2023. Retrieved 31 January 2023.
- "Alvotech and Bioventure Announce Approval of AVT02 (adalimumab) as Simlandi in Saudi Arabia". Alvotech. 24 January 2023. Archived from the original on 26 February 2024. Retrieved 26 February 2024.
- "Celltrion USA Announces U.S. FDA Approval of Yuflyma (adalimumab-aaty), a High-Concentration and Citrate-Free Formulation of Humira (adalimumab) Biosimilar" (Press release). Celltrion. 24 May 2023. Archived from the original on 25 May 2023. Retrieved 28 May 2023 – via Business Wire.
- "Drug Approval Package: Yuflyma injection". U.S. Food and Drug Administration (FDA). 11 August 2023. Archived from the original on 25 August 2023. Retrieved 11 March 2024.
- "So it begins: next Humira biosimilars launch in US". pharmaphorum. 4 July 2023. Archived from the original on 5 July 2023. Retrieved 4 July 2023.
- Wingrove P (30 June 2023). "Analysis: New Humira rivals likely to hit US market with small discounts in July". Reuters. Archived from the original on 30 June 2023. Retrieved 4 July 2023.
- Wingrove P (1 July 2023). "Organon, Samsung Bioepis launch copycat for arthritis drug Humira at 85% discount". Reuters. Archived from the original on 1 July 2023. Retrieved 4 July 2023.
- "Alvotech and Teva Announce U.S. Approval of Simlandi (adalimumab-ryvk) injection, the first interchangeable high-concentration, citrate-free biosimilar to Humira" (Press release). Alvotech. 24 February 2024. Archived from the original on 26 February 2024. Retrieved 26 February 2024 – via GlobeNewswire.
- "Cambridge Antibody Technology prevails in High Court proceedings regarding Humira". www.cambridgenetwork.co.uk. Cambridge Network. 20 December 2004. Archived from the original on 9 January 2021. Retrieved 5 January 2021.
- "Biotech firm wins royalty fight". BBC News Online. 20 December 2004. Archived from the original on 27 August 2021. Retrieved 23 April 2010.
- Murray-West R (27 October 2005). "Drug maker CAT surges after royalty settlement". The Telegraph. London. Archived from the original on 20 September 2018. Retrieved 23 April 2010.
- "Multi-Million Dollar Deal To Benefit Medical Research" (PDF) (Press release). Medical Research Council. Archived from the original (PDF) on 27 June 2007. Retrieved 20 July 2009.
- Centocor Ortho Biotech, Inc. v. Abbott Lab'ys, 669 F. Supp. 2d 756 (E.D. Tex. 2009) Archived 22 March 2022 at the Wayback Machine, rev'd, 636 F.3d 1341 (Fed. Cir. 2011).
- Pierson R, Spicer J (30 June 2009). "Jury returns $1.67 billion drug verdict against Abbott". Reuters. Archived from the original on 2 March 2021. Retrieved 9 September 2019.
- "Centocor Ortho Biotech v. Abbott Laboratories, 636 F. 3d 1341". United States Court of Appeals for the Federal Circuit. 23 February 2011. Archived from the original on 27 August 2021. Retrieved 9 September 2019 – via Google Scholar.
- Decker S (23 February 2011). "Abbott Wins Reversal of J&J's $1.67 Billion Patent Victory". Bloomberg Businessweek. Archived from the original on 6 May 2011.
- Silbersher Z (10 June 2020). "Why was the Humira "patent thicket" antitrust case against AbbVie dismissed?". Markman Advisors. Archived from the original on 20 September 2020. Retrieved 6 October 2020.
- Mayor and City of Baltimore, et al. v. AbbVIE Inc., et al. Archived 3 August 2022 at the Wayback Machine, 7th Circuit Court of Appeals (decided 1 August 2022).
- Hansen K, Kolinsky MA (17 February 2020). "Humira: How far can drug makers go to protect their branded market?". The National Law Review. Archived from the original on 21 January 2022. Retrieved 28 January 2023.
- Rebecca R (28 January 2023). "How a Drug Company Made $114 Billion by Gaming the US Patent System". The New York Times. Archived from the original on 28 January 2023. Retrieved 28 January 2023.
worldcat.org
search.worldcat.org
- Welch B (15 December 2008). "Adalimumab (Humira) for the Treatment of Rheumatoid Arthritis". American Family Physician. 78 (12): 1406–1408. ISSN 0002-838X. Archived from the original on 24 November 2020. Retrieved 9 September 2019.
worldpharmaoutlook.blogspot.com
- Morey S (17 September 2009). "UK – Summary of NICE Approvals in September 2009". Archived from the original on 20 September 2018. Retrieved 4 February 2014.