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Eculizumab

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Not to be confused with ocrelizumab.

Eculizumab
Monoclonal antibody
TypeWhole antibody
SourceHumanized (from mouse)
TargetComplement protein C5
Clinical data
Trade namesSoliris
BiosimilarsBekemv,[1] Elizaria,[2] Bkemv,[3] eculizumab-aagh, eculizumab-aeeb,[3] Epysqli[4]
AHFS/Drugs.comMonograph
MedlinePlusa612024
License data
Pregnancy
category
  • AU: B2
Routes of
administration		Intravenous
Drug classComplement inhibitor
ATC code
Legal status
Legal status
Pharmacokinetic data
Elimination half-life8 to 15 days (mean 11 days)
Identifiers
CAS Number
DrugBank
ChemSpider
  • none
UNII
KEGG
ChEMBL
Chemical and physical data
Molar mass148 kg/mol
 ☒NcheckY (what is this?)  (verify)

Eculizumab, sold under the brand name Soliris among others, is a recombinant humanized monoclonal antibody used to treat paroxysmal nocturnal hemoglobinuria, atypical hemolytic uremic syndrome, generalized myasthenia gravis, and neuromyelitis optica.[8][9] In people with paroxysmal nocturnal hemoglobinuria, it reduces both the destruction of red blood cells and need for blood transfusion, but does not appear to affect the risk of death.[11] Eculizumab was the first medication approved for each of its uses, and its approval was granted based on small trials.[12][13][14][15] It is given by intravenous infusion.[8] It is a humanized monoclonal antibody functioning as a terminal complement inhibitor.[13] It binds to the complement C5 protein and inhibits activation of the complement system, a part of the body's immune system.[16] This binding prevents the breakdown of red blood cells in the bloodstream (intravascular hemolysis) in people with paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome.[16]

The most frequently reported adverse reactions for people with paroxysmal nocturnal hemoglobinuria include headache, nasopharyngitis (common cold), back pain and nausea[16] The most frequently reported adverse reactions for people with atypical hemolytic uremic syndrome include headache, diarrhea, hypertension, upper respiratory infection, abdominal pain, vomiting, nasopharyngitis, anemia, cough, swelling of lower legs or hands, nausea, urinary tract infections and fever[16]

Eculizumab (Soliris) is developed, manufactured, and marketed by Alexion Pharmaceuticals.[17]: 6 

Medical uses

[edit]

Eculizumab is indicated for the treatment of people with paroxysmal nocturnal hemoglobinuria to reduce hemolysis; and the treatment of people with atypical hemolytic uremic syndrome to inhibit complement-mediated thrombotic microangiopathy.[16]

Eculizumab is used to treat atypical hemolytic uremic syndrome (aHUS) and paroxysmal nocturnal hemoglobinuria (PNH).[8][7][15] For people with paroxysmal nocturnal hemoglobinuria, it improves quality of life and decreases the need for blood transfusions but does not appear to affect the risk of death.[11] It does not appear to change the risk of blood clots, myelodysplastic syndrome, acute myelogenous leukemia, or aplastic anemia.[11] Eculizumab is also used to treat neuromyelitis optica spectrum disorder in adults who are anti-aquaporin-4 (AQP4) antibody positive.[12]

Adverse effects

[edit]

Eculizumab carries a boxed warning for the risk of meningococcal infections caused by Neisseria meningitidis.[8][7][16]

Eculizumab inhibits terminal complement activation and therefore makes people vulnerable to infection with encapsulated organisms. Life-threatening and fatal meningococcal infections have occurred in people who received eculizumab.[8] People receiving eculizumab have up to 2,000 times greater risk of developing invasive meningococcal disease.[18] Due to the increased risk of meningococcal infections, meningococcal vaccination is recommended at least 2 weeks prior to receiving eculizumab, unless the risks of delaying eculizumab therapy outweigh the risk of developing a meningococcal infection, in which case the meningococcal vaccine should be administered as soon as possible.[8] Both a serogroup A, C, W, Y conjugate meningococcal vaccine and a serogroup B meningococcal vaccine are recommended for people receiving eculizumab.[19] Receiving the recommended vaccinations may not prevent all meningococcal infections, especially from nongroupable N. meningiditis.[20] In 2017, it became clear that eculizumab has caused invasive meningococcal disease despite vaccination, because it interferes with the ability of antimeningococcal antibodies to protect against invasive disease.[20]

The drug's labels also carry warnings of severe anemia arising from the destruction of red blood cells as well as severe cases of blood clots forming in small blood vessels.[8][7]

Headaches are very common adverse effects, occurring in more than 10% of people who take the drug.[7]

Common adverse effects (occurring in between 1% and 10% of people who take the drug) include infections (pneumonia, upper respiratory tract infection, colds, and urinary tract infection), loss of white blood cells, loss of red blood cells, anaphylactic reaction, hypersensitivity reaction, loss of appetite, mood changes like depression and anxiety, a sense of tingling or numbness, blurred vision, vertigo, ringing in the ears, heart palpitations, high blood pressure, low blood pressure, vascular damage, peritonitis, constipation, upset stomach, swollen belly, itchy skin, increased sweating, blotches from small bleeds under the skin and skin redness, hives, muscle spasms, bone pain, back pain, neck pain, swollen joints, kidney damage, painful urination, spontaneous erections, general edema, chest pain, weakness, pain at the infusion site, and elevated transaminases.[7]

Pharmacology

[edit]

Eculizumab specifically binds to the terminal complement component 5, or C5, which acts at a late stage in the complement cascade.[7] When activated, C5 is involved in activating host cells, thereby attracting pro-inflammatory immune cells, while also destroying cells by triggering pore formation. By inhibiting the complement cascade at this point, the normal, disease-preventing functions of proximal complement system are largely preserved, while the properties of C5 that promote inflammation and cell destruction are impeded.[21]

Eculizumab inhibits the cleavage of C5 by the C5 convertase into C5a, a potent anaphylatoxin with prothrombotic and proinflammatory properties, and C5b, which then forms the terminal complement complex C5b-9 which also has prothrombotic and proinflammatory effects. Both C5a and C5b-9 cause the complement-mediated events that are characteristic of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome.[21]

The metabolism of eculizumab is thought to occur via lysosomal enzymes that cleave the antibody to generate small peptides and amino acids. The volume of distribution of eculizumab in humans approximates that of plasma.[14]

Chemistry

[edit]

Eculizumab is a recombinant humanized monoclonal antibody against the complement protein C5.[13] It is an immunoglobulin G-kappa (IgGκ) consisting of human constant regions and murine complementarity-determining regions grafted onto human framework light and heavy chain variable regions. The compound contains two 448-amino acid heavy chains and two 214-amino acid light chains, and has a molecular weight of approximately 148 kilodaltons (kDa).[14]

Society and culture

[edit]
[edit]

Eculizumab was approved by the US Food and Drug Administration (FDA) in March 2007, for the treatment of paroxysmal nocturnal hemoglobinuria.[14] Eculizumab has exclusivity rights until 2017, which protects it from competition until 2017.[17]: 6  When the FDA approved it in September 2011, for the treatment of atypical hemolytic uremic syndrome, it designated it as an orphan drug.[22] The FDA approval in 2011 was based on two small prospective trials of 17 people and 20 people.[15][8][23]

The European Medicines Agency approved it for the treatment of paroxysmal nocturnal hemoglobinuria in June 2007,[7] and in November 2011, for the treatment of atypical hemolytic uremic syndrome.[24] Health Canada approved it in 2009, to treat paroxysmal nocturnal hemoglobinuria and in 2013, as the only drug to treat atypical hemolytic uremic syndrome.[25]

Eculizumab was approved by the FDA for the treatment of adults with neuromyelitis optica spectrum disorder who are anti-aquaporin-4 (AQP4) antibody positive in 2019, based on the results of the PREVENT trial.[12]

Economics

[edit]

A 2014 study showed that Eculizumab may provide substantive benefits to people with paroxysmal nocturnal hemoglobinuria in terms of life expectancy and quality of life but at a high incremental cost.[26]

In 2010, Alexion priced Soliris as the most expensive drug in the world,[27] at approximately US$409,500 a year in the United States (2010),[27] €430,000 per year for ongoing treatment in the UK,[28][29] and $500,000 a year in Canada (2014).[30] In 2021, Soliris generated US$1.874 billion in sales.[31][32]

In April and May 2013, a controversy arose in Belgium when the media revealed that the government had refused to pay for a seven-year-old boy's treatment because Soliris was too expensive. The boy's medicine cost €9,000 every two weeks.[33] A public relations agency working for Alexion had reportedly been looking for such a story, and helped the boy's parents communicate their story to the press in order to pressure governments to reimburse the cost of the drug.[34][35][36] Several politicians stated that the company was attempting to 'blackmail' the government, charges which Alexion denied.[37] By 7 May 2013, an agreement had been reached for the government to reimburse the cost of the medicine beginning in July 2013.[38][39]

In December 2013, New Zealand's government pharmaceutical buyer Pharmac declined a proposal to subsidize the drug after Alexion refused to budge on a NZ$670,000 (US$590,000) per person per year price and Pharmac's economic analysis determined the price would need to be halved before the drug was cost-effective enough to subsidize.[40] Pharmac's decision upset many people with paroxysmal nocturnal hemoglobinuria in New Zealand,[41] although Pharmac has not ruled out reviewing the decision at a later date, should the drug be made available at a lower price.[40]

In December 2014, the provincial government of Ontario, Canada, negotiated the price with the manufacturer, the only drug approved by Health Canada to treat atypical hemolytic uremic syndrome. People can apply for it on "compassionate grounds" "on a case-by-case basis for example individuals who have been urgently hospitalized due to an immediate life-, limb-, or organ-threatening complication." It then was already "funded by the Ontario government for the treatment of another rare illness, paroxysmal nocturnal hemoglobinuria (PNH), through a bulk-buy deal reached by the provincial premiers in 2011."[30]

In February 2015, Canada's drug-price regulator took the rare step of calling a hearing into Soliris, accusing Alexion of exceeding the permissible price cap under the ""Highest International Price Comparison"" (HIPC).[42] In June 2015, the Patented Medicine Prices Review Board (PMPRB) under the Canadian Patent Act, held a preliminary hearing in Ottawa, Ontario to examine allegations. John Haslam, President and General Manager of Vaughan, Ontario-based Alexion Canada, was named as one of the respondents.[43] Alexion charges Canada $700,000 per person per year, more than anywhere else in the world.[44] Alexion denies the claim. In Canada "provincial drug plans have already negotiated secret discounts on Soliris for many of the patients they cover."[42]

As of 2015, while eculizumab used for paroxysmal nocturnal hemoglobinuria was associated with 1.13 additional life years and 2.45 quality of life years QALYs, there has been a high incremental cost (CAN$5.24 million) and a substantial opportunity cost. A 2014 Canadian study calculated the cost per life-year-gained with treatment as CAN$4.62 million (US$4,571,564) and cost per quality-adjusted-life-year as CAN$2.13 million (US$2,112,398)."The incremental cost per life year and per QALY gained is CAN$4.62 million and CAN$2.13 million, respectively. Based on established thresholds, the opportunity cost of funding eculizumab is 102.3 discounted QALYs per patient funded."[45]

By 2015, industry analysts and academic researchers agreed that the high price of orphan drugs, such as eculizumab, was not related to research, development, and manufacturing costs: their price is arbitrary and they have become more profitable than traditional medicines.[44]

The Brazilian universal health care system has annually provided it for its citizens. Initially patients got access to it by suing the government and demanding the right for treatment. In 2016 it was the medication that gave the biggest cost to the system by the judicial way, accounting to 625 million reais (about US$ 178 million at the time) to treat 364 patients,[46] but it was second when counting all the system regular medications, the biggest cost being sofosbuvir.[47] Brazil's supreme court ruled in April 2018 to break the patent of Soliris in Brazil, enabling it to be produced locally.[48] In December 2018 it was incorporated in the public health care system.[49]

Biosimilars

[edit]
Main article: Biosimilar

A biosimilar branded Elizaria is available in Russia.[2]

In February 2023, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Bekemv, intended for the treatment of adults and children in paroxysmal nocturnal hemoglobinuria.[50] The applicant for this medicinal product is Amgen Technology (Ireland) Unlimited Company.[50] Bekemv is a biosimilar medicinal product.[50] It is highly similar to the reference product Soliris (eculizumab), which was authorized in the EU on 20 June 2007.[50] Data show that Bekemv has comparable quality, safety and efficacy to Soliris.[50] Bekemv was approved for medical use in the European Union in April 2023.[51][1]

Epysqli was approved for medical use in the European Union in May 2023.[4]

In May 2024, eculizumab-aeeb (Bkemv) was approved for medical use in the United States.[16]

Eculizumab-aagh (Epysqli) was approved for medical use in the United States in July 2024.[52]

Research

[edit]

Eculizumab has been explored as a treatment for CD55 deficiency, also known as CHAPLE syndrome, a rare genetic disorder of the immune system.[53]

References

[edit]
  1. ^ a b c "Bekemv". European Medicines Agency (EMA). 15 May 2023. Archived from the original on 16 May 2023. Retrieved 15 May 2023.
  2. ^ a b "Elizaria". Generium. Archived from the original on 3 April 2019. Retrieved 22 May 2019.
  3. ^ a b "Bkemv (eculizumab-aeeb) injection, for intravenous use" (PDF). Archived (PDF) from the original on 29 May 2024. Retrieved 31 May 2024.
  4. ^ a b c "Epysqli EPAR". European Medicines Agency (EMA). 31 May 2023. Archived from the original on 31 May 2023. Retrieved 31 May 2023.
  5. ^ "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.
  6. ^ "Soliris - Summary of Product Characteristics (SmPC)". (emc). 16 July 2021. Archived from the original on 21 May 2022. Retrieved 9 April 2022.
  7. ^ a b c d e f g h "Soliris - Summary of Product Characteristics". UK Electronic Medicines Compendium. 23 March 2017. Archived from the original on 19 February 2018. Retrieved 18 July 2017.
  8. ^ a b c d e f g h i "Soliris- eculizumab injection, solution, concentrate". DailyMed. 20 April 2021. Archived from the original on 9 April 2022. Retrieved 9 April 2022.
  9. ^ a b "Soliris EPAR". European Medicines Agency. 17 September 2018. Archived from the original on 19 October 2019. Retrieved 9 April 2022.
  10. ^ "Epysqli". Union Register of medicinal products. 31 May 2023. Archived from the original on 6 June 2023. Retrieved 6 June 2023.
  11. ^ a b c Martí-Carvajal AJ, Anand V, Cardona AF, Solà I (October 2014). "Eculizumab for treating patients with paroxysmal nocturnal hemoglobinuria". The Cochrane Database of Systematic Reviews. 10 (10): CD010340. doi:10.1002/14651858.CD010340.pub2. PMID 25356860.
  12. ^ a b c "FDA approves first treatment for neuromyelitis optica spectrum disorder, a rare autoimmune disease of the central nervous system" (Press release). U.S. Food and Drug Administration (FDA). 27 June 2019. Archived from the original on 14 September 2019. Retrieved 28 June 2019.
  13. ^ a b c Rother RP, Rollins SA, Mojcik CF, Brodsky RA, Bell L (November 2007). "Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria". Nature Biotechnology. 25 (11): 1256–1264. doi:10.1038/nbt1344. PMID 17989688. S2CID 22732675.
  14. ^ a b c d Dmytrijuk A, Robie-Suh K, Cohen MH, Rieves D, Weiss K, Pazdur R (September 2008). "FDA report: eculizumab (Soliris) for the treatment of patients with paroxysmal nocturnal hemoglobinuria". The Oncologist. 13 (9): 993–1000. doi:10.1634/theoncologist.2008-0086. PMID 18784156. S2CID 21972428.
  15. ^ a b c Keating GM (December 2013). "Eculizumab: a review of its use in atypical haemolytic uraemic syndrome". Drugs. 73 (18): 2053–2066. doi:10.1007/s40265-013-0147-7. PMID 24249647. S2CID 36682579.
  16. ^ a b c d e f g "FDA Approves First Interchangeable Biosimilar for Two Rare Diseases". U.S. Food and Drug Administration. 28 May 2024. Archived from the original on 30 May 2024. Retrieved 31 May 2024. Public Domain This article incorporates text from this source, which is in the public domain.
  17. ^ a b Bourgoin AF, Nuskey B (April 2015). An Outlook on Biosimilar Competition (PDF) (Report). Archived from the original (PDF) on 13 May 2015. Retrieved 29 June 2015.
  18. ^ "HAN Archive - 00404|Health Alert Network (HAN)". emergency.cdc.gov. 7 July 2017. Archived from the original on 9 July 2017. Retrieved 10 July 2017.
  19. ^ Folaranmi T, Rubin L, Martin SW, Patel M, MacNeil JR (June 2015). "Use of Serogroup B Meningococcal Vaccines in Persons Aged ≥10 Years at Increased Risk for Serogroup B Meningococcal Disease: Recommendations of the Advisory Committee on Immunization Practices, 2015". MMWR. Morbidity and Mortality Weekly Report. 64 (22): 608–612. PMC 4584923. PMID 26068564. Archived from the original on 17 August 2021. Retrieved 9 September 2017.
  20. ^ a b McNamara LA, Topaz N, Wang X, Hariri S, Fox L, MacNeil JR (July 2017). "High Risk for Invasive Meningococcal Disease Among Patients Receiving Eculizumab (Soliris) Despite Receipt of Meningococcal Vaccine". MMWR. Morbidity and Mortality Weekly Report. 66 (27): 734–737. doi:10.15585/mmwr.mm6627e1. PMC 5687588. PMID 28704351.
  21. ^ a b Brodsky RA (2009). "Paroxysmal nocturnal hemoglobinuria". In Hoffman R, Benz Jr EJ, Shatill SJ (eds.). Hematology: Basic Principles and Practice (5th ed.). Churchill Livingstone/Elsevier. pp. 385–395. ISBN 978-0-443-06715-0.
  22. ^ "FDA approves Soliris for rare pediatric blood disorder: Orphan drug receives second approval for rare disease" (Press release). U.S. Food and Drug Administration (FDA). 23 September 2011. Archived from the original on 18 January 2017. Retrieved 25 June 2015.
  23. ^ Pollack A (30 April 1990). "Orphan Drug Law Spurs Debate". The New York Times. Archived from the original on 19 February 2019. Retrieved 15 February 2009.
  24. ^ "EU/3/09/653". European Medicines Agency. Archived from the original on 23 September 2017. Retrieved 19 July 2017.
  25. ^ "In The Matter Of The Patent Act, R.S.C., 1985, C. P-4, As Amended" (PDF). Patented Medicine Prices Review Board. 15 January 2015. Archived from the original (PDF) on 21 April 2015.
  26. ^ Coyle D, Cheung MC, Evans GA (November 2014). "Opportunity cost of funding drugs for rare diseases: the cost-effectiveness of eculizumab in paroxysmal nocturnal hemoglobinuria". Medical Decision Making. 34 (8): 1016–1029. doi:10.1177/0272989X14539731. PMID 24990825. S2CID 206498664.
  27. ^ a b Herper M (19 February 2010), "The World's Most Expensive Drugs", Forbes, archived from the original on 28 April 2021, retrieved 25 June 2015
  28. ^ Wall M (5 February 2015). "Doctors must tell patients of errors, under new Varadkar law. Like a motoring 'hit and run' for doctors to fail to make such disclosures, says Minister". Irish Times. Archived from the original on 30 October 2021. Retrieved 5 February 2015.
  29. ^ "High cost of treatment for rare blood disorder needs to be clarified, says NICE in draft guidance". National Institute for Health and Care Excellence. UK. 4 March 2014. Archived from the original on 25 July 2021. Retrieved 24 September 2014.
  30. ^ a b Gallant J (4 December 2014), Toronto woman with rare disease fights province for life-saving but costly drug, The Toronto Star, archived from the original on 14 August 2020, retrieved 26 August 2017
  31. ^ Dunleavy K (6 April 2022). "AAN: AstraZeneca touts new Ultomiris gMG data ahead of potential Argenx showdown". Fierce Pharma. Archived from the original on 9 April 2022. Retrieved 9 April 2022.
  32. ^ Annual report 2021 Archived 22 February 2022 at the Wayback Machine
  33. ^ "Viktor (7) moet elke twee weken infuus krijgen van 9.000 euro" [Viktor (7) must receive an infusion of 9,000 euros every two weeks]. VRT (in Dutch). 30 April 2013. Archived from the original on 27 February 2023. Retrieved 27 February 2023.
  34. ^ Eckert M, Baumers K (4 May 2013). "Pr-bureau van farmabedrijf adviseerde ook ouders Viktor" [Pharmaceutical company's PR agency also advised parents Viktor]. De Standaard (in Dutch). Archived from the original on 27 February 2023. Retrieved 27 February 2023.
  35. ^ "Farmabedrijf Alexion heeft Viktor "gebruikt"" [Pharmaceutical company Alexion has "used" Viktor]. VRT (in Dutch). 4 May 2013. Archived from the original on 27 February 2023. Retrieved 27 February 2023.
  36. ^ "Farmabaas fluit Alexion terug in zaak-Viktor" [Pharma boss Alexion whistles back in Viktor case]. De Standaard (in Dutch). 6 May 2013. Archived from the original on 27 February 2023. Retrieved 27 February 2023.
  37. ^ "Detiège: "Dit is chantage van het farmabedrijf"" [Detiège: "This is blackmail from the pharmaceutical company"]. VRT (in Dutch). 2 May 2013. Archived from the original on 27 February 2023. Retrieved 27 February 2023.
  38. ^ "Medicijn Viktor vanaf juli terugbetaald" [Viktor medicine reimbursed from July]. De Standaard (in Dutch). 7 May 2013. Archived from the original on 10 June 2013. Retrieved 27 February 2023.
  39. ^ "Contract van Onkelinx met farmareus opent doos van Pandora" [Onkelinx contract with pharmaceutical giant opens Pandora's box]. De Morgen. 23 March 2015. Archived from the original on 27 February 2023. Retrieved 27 February 2023.
  40. ^ a b "Citing unreasonable price, PHARMAC declines eculizumab funding proposal". Pharmaceutical Management Agency. 11 December 2013. Archived from the original on 24 September 2015. Retrieved 22 June 2014.
  41. ^ "Plea to Pharmac for pricey life-saver". 3 News NZ. 24 January 2013. Archived from the original on 12 December 2013. Retrieved 26 June 2015.
  42. ^ a b Blackwell T (3 February 2015), "World's most expensive drug — which costs up to $700,000 per year — too expensive, Canada says", National Post, archived from the original on 30 October 2021, retrieved 25 June 2015
  43. ^ "Motions and Exhibits" (PDF), Government of Canada, Ottawa, Ontario, 2015, archived (PDF) from the original on 18 April 2020, retrieved 25 June 2015
  44. ^ a b Crowe K (25 June 2015), "How pharmaceutical company Alexion set the price of the world's most expensive drug: Cost of one of world's most expensive drugs shrouded in corporate secrecy", CBC News, archived from the original on 26 June 2015, retrieved 25 June 2015
  45. ^ Coyle D, Cheung MC, Evans GA (November 2014). "Opportunity cost of funding drugs for rare diseases: the cost-effectiveness of eculizumab in paroxysmal nocturnal hemoglobinuria". Medical Decision Making. 34 (8): 1016–1029. doi:10.1177/0272989X14539731. PMID 24990825. S2CID 206498664.
  46. ^ Xavier C (2018). "Judicialização da Saúde: Perspectiva crítica sobre os gastos da União para o cumprimento das ordens judiciais" (PDF). Coletânea direito à saúde: Dilemas do fenômeno da judicialização da saúde (in Portuguese). 2: 52–61. Archived (PDF) from the original on 20 May 2022. Retrieved 4 May 2022.
  47. ^ Chaves GC, Vieira MC, Costa RD, Vianna MN (2018). Medicamentos em situação de exclusividade financiados pelo Ministério da Saúde: análise da situação patentária e das compras públicas (PDF) (in Portuguese). Rio de Janeiro: Fiocruz, ENSP. ISBN 978-85-9511-029-8. Archived (PDF) from the original on 20 May 2022. Retrieved 4 May 2022.
  48. ^ Brito R (19 April 2019). "STJ atende a pedido da AGU e quebra patente do medicamento Soliris" [STJ responds to AGU's request and breaks patent on Soliris drug]. Reuters (in Portuguese). Archived from the original on 16 June 2018.
  49. ^ Torna pública a decisão de incorporar o eculizumabe para tratamento de pacientes com hemoglobinúria paroxística noturna (HPN) no âmbito do Sistema Único de Saúde - SUS [Makes public the decision to incorporate eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria (PNH) within the scope of SUS] (Ordinance, 77) (in Portuguese). 14 December 2018. "PORTARIA Nº 77, DE 14 DE DEZEMBRO DE 2018 - Imprensa Nacional". Archived from the original on 28 February 2023. Retrieved 19 May 2022.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  50. ^ a b c d e "Bekemv: Pending EC decision". European Medicines Agency (EMA). 24 February 2023. Archived from the original on 24 February 2023. Retrieved 24 February 2023. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  51. ^ "Bekemv". Union Register of medicinal products. 20 April 2023. Archived from the original on 21 April 2023. Retrieved 23 April 2023.
  52. ^ "FDA Approves Samsung Bioepis' Epysqli (eculizumab-aagh) as a Biosimilar to Soliris (eculizumab)" (Press release). Samsung Bioepis. 22 July 2024. Retrieved 23 July 2024 – via GlobeNewswire.
  53. ^ Kurolap A, Eshach Adiv O, Hershkovitz T, Tabib A, Karbian N, Paperna T, et al. (March 2019). "Eculizumab Is Safe and Effective as a Long-term Treatment for Protein-losing Enteropathy Due to CD55 Deficiency". Journal of Pediatric Gastroenterology and Nutrition. 68 (3): 325–333. doi:10.1097/MPG.0000000000002198. PMID 30418410. S2CID 53281594.
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