Etanercept
|
Clinical data |
Trade names |
Enbrel |
AHFS/Drugs.com |
Monograph |
Pregnancy
category |
- AU: B2
- US: B (No risk in non-human studies)
|
Routes of
administration |
Subcutaneous |
ATC code |
|
Legal status |
Legal status |
- AU: S4 (Prescription only)
- UK: POM (Prescription only)
- US: ℞-only
|
Pharmacokinetic data |
Bioavailability |
58–76% (SC) |
Metabolism |
Reticuloendothelial system (speculative) |
Biological half-life |
70–132 hours |
Identifiers |
CAS Number |
|
PubChem SID |
|
DrugBank |
|
ChemSpider |
|
UNII |
|
KEGG |
|
ChEMBL |
|
ECHA InfoCard |
100.224.383 |
Chemical and physical data |
Formula |
C2224H3475N621O698S36 |
Molar mass |
51234.9 g/mol |
Etanercept (trade name Enbrel) is a biopharmaceutical that treats autoimmune diseases by interfering with tumor necrosis factor (TNF; a soluble inflammatory cytokine) by acting as a TNF inhibitor. It has U.S. F.D.A. approval to treat rheumatoid arthritis, juvenile rheumatoid arthritis and psoriatic arthritis, plaque psoriasis and ankylosing spondylitis. TNF-alpha is the "master regulator" of the inflammatory (immune) response in many organ systems. Autoimmune diseases are caused by an overactive immune response. Etanercept has the potential to treat these diseases by inhibiting TNF-alpha.[1]
Etanercept is a fusion protein produced by recombinant DNA. It fuses the TNF receptor to the constant end of the IgG1 antibody. First, the developers isolated the DNA sequence that codes the human gene for soluble TNF receptor 2, which is a receptor that binds to tumor necrosis factor-alpha. Second, they isolated the DNA sequence that codes the human gene for the Fc end of immunoglobulin G1 (IgG1). Third, they linked the DNA for TNF receptor 2 to the DNA for IgG1 Fc. Finally, they expressed the linked DNA to produce a protein that links the protein for TNF receptor 2 to the protein for IgG1 Fc. The prototypic fusion protein was first synthesized and shown to be highly active and unusually stable as a modality for blockade of TNF in vivo in the early 1990s by Bruce A. Beutler, an academic researcher then at the University of Texas Southwestern Medical Center at Dallas, and his colleagues.[2][3][4] These investigators also patented the protein,[5] selling all rights to its use to Immunex, a biotechnology company that was acquired by Amgen in 2002.[6]
It is a large molecule, with a molecular weight of 150 kDa., that binds to TNFα and decreases its role in disorders involving excess inflammation in humans and other animals, including autoimmune diseases such as ankylosing spondylitis,[7] juvenile rheumatoid arthritis, psoriasis, psoriatic arthritis, rheumatoid arthritis, and, potentially, in a variety of other disorders mediated by excess TNFα.
Contents
- 1 Medical uses
- 2 Safety
- 3 Mechanism of action
- 4 Structure
- 5 History
- 6 Society and culture
- 6.1 Marketing
- 6.2 Sales
- 6.3 Patents
- 7 Research
- 8 Similar agents
- 9 References
- 10 External links
Medical uses
In the USA the FDA has licensed Enbrel for :
- Moderate to Severe Rheumatoid Arthritis (RA) (Nov 1998)[8]
- Moderate to Severe Polyarticular Juvenile Rheumatoid Arthritis (May 1999)[9]
- Psoriatic Arthritis (Jan 2002)[10]
- Ankylosing Spondylitis (AS) (July 2003)[11][12]
- Moderate to Severe Plaque Psoriasis (April 2004)[13]
Safety
On May 2, 2008, the FDA placed a black box warning on etanercept due to a number of serious infections associated with the drug.[14] Serious infections and sepsis, including fatalities, have been reported with the use of Etanercept including reactivation of latent tuberculosis and hepatitis B infections.[15][16]
There has also been a report of strongyloides hyperinfection after use of Etanercept.[17]
Mechanism of action
It reduces the effect of naturally present TNF, and hence is a TNF inhibitor, functioning as a decoy receptor that binds to TNF.[18]
Tumor necrosis factor-alpha (TNFα) is a cytokine produced by lymphocytes and macrophages, two types of white blood cells. It mediates the immune response by attracting additional white blood cells to sites of inflammation, and through additional molecular mechanisms which initiate and amplify inflammation. Inhibition of its action by etanercept reduces the inflammatory response which is especially useful for treating autoimmune diseases.
There are two types of TNF receptors: those found embedded in white blood cells that respond to TNF by releasing other cytokines, and soluble TNF receptors which are used to deactivate TNF and blunt the immune response. In addition, TNF receptors are found on the surface of virtually all nucleated cells (red blood cells, which are not nucleated, do not contain TNF receptors on their surface). Etanercept mimics the inhibitory effects of naturally occurring soluble TNF receptors, the difference being that etanercept, because it is a fusion protein rather than a simple TNF receptor, has a greatly extended half-life in the bloodstream, and therefore a more profound and long-lasting biologic effect than a naturally occurring soluble TNF receptor.[19]
Structure
Etanercept is made from the combination of two naturally occurring soluble human 75-kilodalton TNF receptors linked to an Fc portion of an IgG1.[20] The effect is an artificially engineered dimeric fusion protein.[20]
History
Etanercept was developed by researchers at Immunex, and was released for commercial use in late 1998, soon after the release of infliximab (Remicade), which was the first chimeric monoclonal antibody against TNFα to be marketed for clinical use.
Etanercept is a dimeric molecule,[21] and this dimeric structure is necessary for its proper therapeutic activity. During its development at Immunex Corporation an earlier monomeric version did not have sufficient biologic activity.
Society and culture
Marketing
In North America, etanercept is marketed by Amgen under the trade name Enbrel in two separate formulations, one in powder form, the other as a pre-mixed liquid. Wyeth [now part of Pfizer] was the sole marketer of Enbrel outside North America excluding Japan where Takeda Pharmaceuticals markets the drug.
Sales
The U.S. retail price of Enbrel has risen over time. In 2008, the cost of Enbrel was reported to be $1,500 per month or $18,000 per year.[22] By 2011, the cost had reportedly exceeded $20,000 per year.[23][24] In 2013, a survey by the International Federation of Health Plans (IFHP) found that the average U.S. cost for Enbrel was $2,225 per month, or $26,700 per year.[25] The IFHP report also found wide variation in prices charged to various U.S. health plans, between $1,946 per month at the 25th percentile and $4,006 per month at the 95th percentile.[25]
Enbrel is more expensive in the U.S. than in other countries.[25] As of 2013, average monthly costs in surveyed nations ranged from $1,017 in Switzerland to $1,646 in Canada, compared to an average monthly cost of $2,225 per month in the U.S.[25]
Amgen sells Enbrel within the U.S. and Canada, while Pfizer, Inc. sells the drug outside of the U.S. and Canada.[23] Sales within the U.S. and Canada were $3.5 billion in 2010.[23] Sales of Enbrel outside the U.S. and Canada were $3.3 billion in 2010.[26]
Patents
The patent on Enbrel was originally set to expire on October 23, 2012,[27] but, in the United States, a second patent, granting exclusivity for another 16 years, has been granted.[28] Before the extension it seemed unlikely that a generic would have been available. As a biologic, etanercept is subject to different laws from those applicable to chemical formulations. Currently many countries do not permit the manufacture of generic biologics. However, the European Union and the United States (Biologics Price Competition and Innovation Act of 2009) do currently have in place a system to approve generic biologics (biosimilars) which "requires mandatory clinical testing and periodic review".[29]
In April 2013, the Indian pharma major Cipla made an announcement about launching the first biosimilar of Etanercept in India under the brand name 'Etacept' for the treatment of rheumatic disorders. The company's April 17, 2013 press release claimed that the biosimilar will cost 30% less as compared to the innovator.[30]
In January 2015, Samsung and Biogen's joint venture "Samsung Bioepis" successfully submitted Benepali, a biosimilar version of the drug, for review to the European Medicines Agency (EMA), and announced that it will seek regulatory approvals in other territories as well. Later the same year, the European Medicines Agency also accepted Sandoz’s application for review of its etanercept product that will be marketed by Novartis.[31]
In the US, Sandoz submitted a biologics license application (BLA) for the proposed etanercept product "GP2015" in July 2016. Upon acceptance of the first application process, the U.S. FDA reviewed data from European clinical trials and bio-analytical investigations, demonstrating the biosimilarity of GP2015 to the US-licensed Enbrel. Sandoz in 2009 tried to invalidate the patents held by Hoffman-La Roche/Immunex and exclusively licensed to Amgen but lost in federal court. Sandoz was then countersued by Amgen for patent infringements related to the methods of treating psoriasis and/or psoriatic arthritis. The case Immunex Corp. et al. vs. Sandoz Inc. et al., 16-cv-01118-CCC-JBC (D.N.J.) is pending.[32]
Research
Etanercept is being studied as treatment for a number of diseases. This includes certain forms of vasculitis (such as granulomatosis with polyangiitis, in which it was not effective).[33]
Similar agents
- Soluble TNF receptor
- Anti-TNF monoclonal antibodies
- Infliximab
- Adalimumab
- Certolizumab pegol
- Golimumab
References
|
Wikimedia Commons has media related to Etanercept. |
- ^ Feldmann M, Maini RN (October 2003). "TNF defined as a therapeutic target for rheumatoid arthritis and other autoimmune diseases". Nature Medicine. 9: 1245–1250. doi:10.1038/nm939. PMID 14520364. Retrieved 2008-01-10.
- ^ Peppel, K. (1 December 1991). "A tumor necrosis factor (TNF) receptor-IgG heavy chain chimeric protein as a bivalent antagonist of TNF activity". Journal of Experimental Medicine. 174 (6): 1483–1489. doi:10.1084/jem.174.6.1483. PMC 2119031 . PMID 1660525.
- ^ Peppel K.; et al. (1993). "Expression of a TNF inhibitor in transgenic mice". J.Immunol. 151 (10): 5699–703.
- ^ Kolls J.; et al. (1994). "Prolonged and effective blockade of tumor necrosis factor activity through adenovirus-mediated gene transfer". Proc. Natl. Acad. Sci. USA. 91 (1): 215–9.
- ^ U.S. Patent number: 5,447,851
- ^ "Arthritis Drug Effective for Depression in Psoriasis Sufferers". Retrieved 2008-01-10.
- ^ Braun J, McHugh N, Singh A, Wajdula JS, Sato R (2007). "Improvement in patient-reported outcomes for patients with ankylosing spondylitis treated with etanercept 50 mg once-weekly and 25 mg twice-weekly". Rheumatology (Oxford). 46 (6): 999–1004. doi:10.1093/rheumatology/kem069. PMID 17389658.
- ^ Siegel, Jay P. (November 2, 1998). "Approval of Etanercept for treatment of rheumatoid arthritis" (PDF) (Letter). Letter to Sally Gould. Food and Drug Administration. Retrieved April 14, 2015.
- ^ Weiss, Karen D. (May 27, 1999). "Approval of Etanercept for treatment of polyarticular course juvenile rheumatoid arthritis (JRA)" (PDF) (Letter). Letter to Sally Gould. Food and Drug Administration. Retrieved April 14, 2015.
- ^ Weiss, Karen D. (January 15, 2002). "Approval of Etanercept for treatment of psoriatic arthritis" (Letter). Letter to Sally Gould. Food and Drug Administration. Retrieved April 14, 2015.
- ^ Keegan, Patricia (July 24, 2003). "Approval of Etanercept for treatment of ankylosing spondylitis" (PDF) (Letter). Letter to Douglas Hunt. Food and Drug Administration. Retrieved April 14, 2015.
- ^ Maxwell, LJ; Zochling, J; Boonen, A; Singh, JA; Veras, MM; Tanjong Ghogomu, E; Benkhalti Jandu, M; Tugwell, P; Wells, GA (18 April 2015). "TNF-alpha inhibitors for ankylosing spondylitis.". The Cochrane database of systematic reviews. 4: CD005468. doi:10.1002/14651858.CD005468.pub2. PMID 25887212.
- ^ Walton, Marc (April 30, 2004). "Approval of Etanercept for treatment of moderate to severe plaque psoriasis" (PDF) (Letter). Letter to Douglas Hunt. Food and Drug Administration. Retrieved April 14, 2015.
- ^ "Wyeth and Amgen heighten warning of life-threatening infections on skin drug Enbrel". Archived from the original on 2008-05-05. Retrieved 2008-05-02.
- ^ Safety Update on TNF- α Antagonists: Infliximab and Etanercept (PDF). Food and Drug Administration. pp. 13–14. Retrieved 20 December 2013.
- ^ "Prescribing Information - ENBREL". Retrieved 2008-01-10.
- ^ http://www.uptodate.com/contents/strongyloidiasis/abstract/67?utdPopup=true
- ^ Zalevsky J, Secher T, Ezhevsky SA, et al. (August 2007). "Dominant-negative inhibitors of soluble TNF attenuate experimental arthritis without suppressing innate immunity to infection". J. Immunol. 179 (3): 1872–83. doi:10.4049/jimmunol.179.3.1872. PMID 17641054.
- ^ Madhusudan S, Muthuramalingam SR, Braybrooke JP, et al. (2005). "Study of etanercept, a tumor necrosis factor-alpha inhibitor, in recurrent ovarian cancer". J. Clin. Oncol. 23 (25): 5950–9. doi:10.1200/JCO.2005.04.127. PMID 16135466.
- ^ a b Smola, M. G.; Soyer, H. P.; Scharnagl, E (1991). "Surgical treatment of dermatofibrosarcoma protuberans. A retrospective study of 20 cases with review of literature". European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. 17 (5): 447–53. PMID 1936291.
- ^ Smith KJ, Skelton HG (2001). "Rapid onset of cutaneous squamous cell carcinoma in patients with rheumatoid arthritis after starting tumor necrosis factor alpha receptor IgG1-Fc fusion complex therapy". J. Am. Acad. Dermatol. 45 (6): 953–6. doi:10.1067/mjd.2001.117725. PMID 11712048.
- ^ What's behind the whopping price tags on the newest generation of drugs; The story behind the production of Enbrel, Amgen's popular rheumatoid arthritis drug, provides insights as to why bioengineered drugs are so expensive. Carol M. Ostrom, Seattle Times, August 18, 2008
- ^ a b c Patent for Amgen Drug May Undercut Health Care Plan, By ANDREW POLLACK, New York Times, November 23, 2011
- ^ Co-pay hike a painful reality; Miracle drug monthly cost jumps from $42 to $600, By Margery Eagan, Boston Herald, November 3, 2011
- ^ a b c d "2013 Comparative Price Report" (PDF). International Federation of Health Plans. Retrieved 2015-08-14.
- ^ Pfizer, Inc. (2010). 2010 Financial Report.
- ^ http://www.uspto.gov/patents/resources/terms/156.html
- ^ http://www.burrillreport.com/article-amgen_issued_new_patent_on_ra_drug_enbrel.html
- ^ http://www.law.duke.edu/journals/dltr/articles/2008dltr0009.html
- ^ http://www.cipla.com/CiplaSite/Media/PDF/News-Archives/Press-Release-Launch-of-first-biosimilar-of-Etanercept-in-India.pdf?ext=.pdf
- ^ Biosimilar etanercept submitted for approval in EU GaBI Online - Generics and Biosimilars Initiative (Jan 2015). Retrieved 13 July 2016.
- ^ FDA Briefing Document Arthritis Advisory Committee Meeting July 13, 2016. FDA AAC Brief. BLA 761042, GP2015, a proposed biosimilar to Enbrel. Retrieved 13 July 2016.
- ^ Wegener's Granulomatosis Etanercept Trial (WGET) Research Group (2005). "Etanercept plus standard therapy for Wegener's granulomatosis". N. Engl. J. Med. 352 (4): 351–61. doi:10.1056/NEJMoa041884. PMID 15673801.
External links
- Amgen/Wyeth Enbrel site
- A case study on the development of Enbrel until Immunex's acquisition by Amgen
Immunosuppressive drugs / Immunosuppressants (L04)
|
|
Intracellular
(initiation) |
Antimetabolites |
- purine synthesis inhibitors: Azathioprine
- Mycophenolic acid
- pyrimidine synthesis inhibitors: Leflunomide
- Teriflunomide
|
|
Macrolides/
other IL-2 inhibitors |
- FKBP/Cyclophilin/Calcineurin: Tacrolimus
- Ciclosporin
- Pimecrolimus
|
|
IMiDs |
- Lenalidomide
- Pomalidomide
- Thalidomide
- PDE4 inhibitor: Apremilast
|
|
|
Intracellular
(reception) |
IL-1 receptor antagonists |
|
|
mTOR |
- Sirolimus
- Everolimus
- Ridaforolimus
- Temsirolimus
- Umirolimus
- Zotarolimus
|
|
|
Extracellular |
Antibodies |
Monoclonal |
Serum target
(noncellular) |
- Complement component 5 (Eculizumab)
- TNF (Adalimumab
- Afelimomab
- Certolizumab pegol
- Golimumab
- Infliximab
- Nerelimomab)
- Interleukin 5 (Mepolizumab)
- Immunoglobulin E (Omalizumab)
- IL-12 and IL-23 (Lebrikizumab
- Ustekinumab)
|
|
Cellular target |
- CD3 (Muromonab-CD3
- Otelixizumab
- Teplizumab
- Visilizumab)
- CD4 (Clenoliximab
- Keliximab
- Zanolimumab)
- CD11a (Efalizumab)
- CD18 (Erlizumab)
- CD20 (Obinutuzumab
- Rituximab
- Ocrelizumab
- Pascolizumab)
- CD23 (Gomiliximab
- Lumiliximab)
- CD40 (Teneliximab
- Toralizumab)
- CD62L/L-selectin (Aselizumab)
- CD80 (Galiximab)
- CD147/Basigin (Gavilimomab)
- CD154 (Ruplizumab)
- BLyS (Belimumab
- Blisibimod)
- CTLA-4 (Ipilimumab
- Tremelimumab)
- CAT (Bertilimumab
- Lerdelimumab
- Metelimumab)
- Integrin (Natalizumab)
- Interleukin-6 receptor (Tocilizumab)
- LFA-1 (Odulimomab)
- IL-2 receptor/CD25 (Basiliximab
- Daclizumab
- Inolimomab)
- T-lymphocyte (Zolimomab aritox)
|
|
Unsorted |
- Atorolimumab
- Cedelizumab
- Fontolizumab
- Maslimomab
- Morolimumab
- Pexelizumab
- Reslizumab
- Rovelizumab
- Siplizumab
- Talizumab
- Telimomab aritox
- Vapaliximab
- Vepalimomab
|
|
|
Polyclonal |
- Anti-thymocyte globulin
- Anti-lymphocyte globulin
|
|
|
-cept (Fusion) |
- CTLA-4 (Abatacept
- Belatacept)
- TNF inhibitor (Etanercept
- Pegsunercept)
- Aflibercept
- Alefacept
- Rilonacept
|
|
Cytokine receptor modulators
|
|
Chemokine |
|
|
CSF |
Erythropoietin
|
- Agonists: ARA-290
- Asialo erythropoietin
- Carbamylated erythropoietin
- CNTO-530
- Darbepoetin alfa
- Epoetin alfa
- Epoetin beta
- Epoetin delta
- Epoetin epsilon
- Epoetin gamma
- Epoetin kappa
- Epoetin omega
- Epoetin theta
- Epoetin zeta
- Erythropoietin (EPO)
- Erythropoietin-Fc
- Methoxy polyethylene glycol-epoetin beta (CERA/Mircera)
- Peginesatide
- Pegol sihematide (EPO-018B)
|
|
G-CSF (CSF3)
|
- Agonists: Filgrastim
- Granulocyte colony-stimulating factor
- Lenograstim
- Leridistim
- Lipegfilgrastim
- Nartograstim
- Pegfilgrastim
- Pegnartograstim
|
|
GM-CSF (CSF2)
|
- Agonists: Ecogramostim
- Granulocyte macrophage colony-stimulating factor
- Milodistim
- Molgramostim
- Regramostim
- Sargramostim
- Antibodies: Mavrilimumab
- MOR103
- Namilumab
|
|
M-CSF (CSF1)
|
- Agonists: Cilmostim
- Interleukin-34
- Lanimostim
- Macrophage colony-stimulating factor
- Mirimostim
- Kinase inhibitors: Agerafenib
|
|
SCF (c-Kit)
|
|
|
Thrombopoietin
|
- Agonists: Eltrombopag
- Pegacaristim
- Promegapoietin
- Romiplostim
- Thrombopoietin (THPO, MGDF)
|
|
|
Interferon |
IFNAR (α/β, I)
|
- Agonists: Albinterferon
- Interferon alpha (interferon alfa, IFN-α)
- Interferon alfa (IFNA1, IFNA2, IFNA4, IFNA5, IFNA6, IFNA7, IFNA8, IFNA10, IFNA13, IFNA14, IFNA16, IFNA17, IFNA21)
- Interferon alfa 2a
- Interferon alfa 2b
- Interferon alfa n1
- Interferon alfacon-1
- Interferon alpha-n3
- Interferon beta (IFN-β) (IFNB1, IFNB3)
- Interferon beta 1a
- Interferon beta 1b
- Interferon kappa (IFN-ε/κ/τ/ζ, IFNK)
- Interferon omega (IFN-ω, IFNW1)
- Peginterferon alfa-2a
- Peginterferon alfa-2b
- Antibodies: Anifrolumab
- Faralimomab
- MEDI-545
- Rontalizumab
- Sifalimumab
- Decoy receptors: Bifarcept
|
|
IFNGR (γ, II)
|
- Agonists: Interferon gamma (IFN-γ)
- Interferon gamma 1b
- Antibodies: Emapalumab
- Fontolizumab
|
|
IFNLR (λ, III)
|
- See IL-28R (IFNLR) here instead.
|
|
|
Interleukin |
|
|
TGFβ |
|
|
TNF |
|
|
Others |
JAK
(inhibitors)
|
JAK1
|
- Baricitinib
- Filgotinib
- Momelotinib
- Oclacitinib
- Ruxolitinib
- Tofacitinib (tasocitinib, CP-690550)
- Upadacitinib
|
|
JAK2
|
- AG-490
- Atiprimod
- AZD-1480
- Baricitinib
- CHZ868
- Cucurbitacin I (elatericin B, JSI-124)
- CYT387
- Lestaurtinib
- NSC-7908
- NSC-33994
- Pacritinib
- Ruxolitinib
- SD-1008
- Tofacitinib (tasocitinib, CP-690550)
|
|
JAK3
|
- AG-490
- Cercosporamide
- TCS-21311
- Tofacitinib (tasocitinib, CP-690550)
- WHI-P 154
- ZM-39923
- ZM-449829
|
|
|
Others
|
- Additional cytokines: Cardiotrophin 1 (CT-1)
- FMS-like tyrosine kinase 3 ligand (FLT3L)
- Leukemia/leukocyte inhibitory factor (LIF)
- Oncostatin M (OSM)
- Thymic stromal lymphopoietin (TSLP)
- Additional cytokine receptor modulators: Emfilermin
- Lestaurtinib
- Midostaurin
- Quizartinib
- Sorafenib
- Sunitinib
|
|
|
- See also: Receptor/signaling modulators
- Signaling peptide/protein receptor modulators
- Growth factor receptor modulators
|