Etanercept: Difference between revisions
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==Sales== |
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Enbrel is the most widely used anti-TNF biologic drug in the field of [[rheumatology]] with more patients taking this drug for that indication than either Remicade ([[infliximab]]) or Humira ([[adalimumab]]){{Fact|date=June 2007}}. Infliximab is the most widely used anti-TNF biologic drug when all FDA approved indications (uses) of the drugs are considered, including [[Crohn's disease]] and [[ulcerative colitis]], two autoimmune diseases for which etanercept does not have an FDA approved indication. In addition to their labeled indications, there are multiple published, peer-reviewed scientific studies suggesting potential uses for off-label indications, for which the FDA has not verified either safety or efficacy. |
Enbrel is the most widely used anti-TNF biologic drug in the field of [[rheumatology]] with more patients taking this drug for that indication than either Remicade ([[infliximab]]) or Humira ([[adalimumab]]){{Fact|date=June 2007}}. Is Wyeth writing this article?? - if you are going to make a statement like that you need to back it up. Infliximab is the most widely used anti-TNF biologic drug when all FDA approved indications (uses) of the drugs are considered, including [[Crohn's disease]] and [[ulcerative colitis]], two autoimmune diseases for which etanercept does not have an FDA approved indication. In addition to their labeled indications, there are multiple published, peer-reviewed scientific studies suggesting potential uses for off-label indications, for which the FDA has not verified either safety or efficacy. |
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==Experimental/off-label uses== |
==Experimental/off-label uses== |
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Revision as of 03:25, 25 July 2008
| File:ENBREL.jpg | |
| Clinical data | |
|---|---|
| Pregnancy category | |
| Routes of administration | Subcutaneous |
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | 58–76% (SC) |
| Metabolism | Reticuloendothelial system (speculative) |
| Elimination half-life | 70–132 hours |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| DrugBank | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.224.383 |
| Chemical and physical data | |
| Formula | C2224H3475N621O698S36 |
| Molar mass | 51234.9 g/mol g·mol−1 |
Etanercept (Enbrel) is a recombinant-DNA drug made by combining two proteins (a fusion protein). It links human soluble TNF receptor to the Fc component of human immunoglobulin G1 (IgG1).
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,[2] juvenile rheumatoid arthritis, psoriasis, psoriatic arthritis, rheumatoid arthritis, and, potentially, in a variety of other disorders mediated by excess TNFα.
This therapeutic potential is based on the fact that TNF-alpha is the "master regulator" (as coined by Marc Feldmann, Phd, and Ravinder N. Maini BCh, recipients of the 2003 Lasker Award for their anti-TNF research in rheumatoid arthritis) of the inflammatory response in many organ systems. [3]
In the United States and the United Kingdom, etanercept is co-marketed by Amgen and Wyeth under the trade name Enbrel in two separate formulations, one in powder form, the other as a pre-mixed liquid.
Development
Etanercept was developed by researchers at biotechnology company Immunex, which was subsequently acquired by Amgen in 2002.[4] It was released for commercial use in late 1998, soon after the release of infliximab (Remicade) – the first chimeric monoclonal antibody against TNFα to be marketed for clinical use.
Etanercept is a dimeric molecule,[5] 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.
Mode of action
Tumor necrosis factor-alpha (TNFα) is a cytokine produced by monocytes and macrophages, two types of white blood cells. It mediates the immune response by increasing the transport of 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.[6]
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. The effect is an artificially engineered dimeric fusion protein.
Administration
Enbrel is marketed as a lyophylized powder in 25 mg vials which must be reconstituted with a diluent and then injected subcutaneously, typically by the patient at home.
Because patients with arthritis found the reconstitution procedure difficult, it was made available as pre-filled 50 mg/ml syringes in late 2004 and a single-use 50 mg autoinjector "pen" was brought to market in mid-2006. [7]
It cannot be administered orally, because the digestive system would destroy the drug.
FDA approved dose is 25 mg BIW (twice weekly) or 50 mg QW (once weekly).
Safety
All TNF inhibitors are immunosuppressants. After a number of studies and reports of adverse reactions in patients receiving anti-TNF alpha therapy (including serious and sometimes fatal blood disorders, infections, rare reports of lymphoma and solid tissue cancers, rare reports of serious liver injury, and rare reports of demyelinating central nervous system disorders), rare reports of congestive heart failure, the U.S. Food and Drug Administration issued a warning to doctors appearing in the respective product labeling of these drugs instructing them to screen and monitor potential patients more carefully. [8]
Although these three agents are all biologic anti-TNF therapeutics, their methods of administration, dosing, and side effect profiles are somewhat different. These differences may be accounted for by fundamental differences in their biologic structure. Both infliximab and adalimumab fix complement, and have the ability to lyze cells. While potentially contributing to their therapeutic efficacy in disorders such as Crohn's disease (for which both of these monoclonal antibodies are now FDA-approved), these mABs also carry black-box warnings which are not shared by etanercept. In addition infliximab has a higher propensity for the development of anaphylaxis, perhaps as a result both of its chimeric structure and its intravenous route of administration.
On May 2, 2008, the FDA placed a black box warning on etanercept due to a number of serious infections associated with the drug. [9]
Sales
Enbrel is the most widely used anti-TNF biologic drug in the field of rheumatology with more patients taking this drug for that indication than either Remicade (infliximab) or Humira (adalimumab)[citation needed]. Is Wyeth writing this article?? - if you are going to make a statement like that you need to back it up. Infliximab is the most widely used anti-TNF biologic drug when all FDA approved indications (uses) of the drugs are considered, including Crohn's disease and ulcerative colitis, two autoimmune diseases for which etanercept does not have an FDA approved indication. In addition to their labeled indications, there are multiple published, peer-reviewed scientific studies suggesting potential uses for off-label indications, for which the FDA has not verified either safety or efficacy.
Experimental/off-label uses
Given the central role of TNF-alpha in many diseases, etanercept is being studied as treatment for a number of these disease, including over 150 clinical trials.[10] This includes certain forms of vasculitis (such as Wegener's granulomatosis, in which it was not effective).[11]
A 2006 pilot study showed small but significant improvements in various cognitive rating scales in patients with Alzheimer's disease after treatment with etanercept.[12] A further study, administering to a single AD patient via perispinal infusion, showed rapid and significant improvement in Alzheimer's symptoms.[13]
Similar agents
References
- ^ "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 Oct 2023.
- ^ 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.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ "TNF defined as a therapeutic target for rheumatoid arthritis and other autoimmune diseases - Nature Medicine". Retrieved 2008-01-10.
- ^ "Arthritis Drug Effective for Depression in Psoriasis Sufferers". Retrieved 2008-01-10.
- ^ 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.
- ^ 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.
{{cite journal}}: Explicit use of et al. in:|author=(help)CS1 maint: multiple names: authors list (link) - ^ "Enbrel and Humira Now Have Automated Delivery System". Retrieved 2008-01-10.
- ^ "Prescribing Information - ENBREL". Retrieved 2008-01-10.
- ^ "Wyeth and Amgen heighten warning of life-threatening infections on skin drug Enbrel". Retrieved 2008-05-02.
- ^ FDA Clinical Trials database
- ^ "Etanercept plus standard therapy for Wegener's granulomatosis". N. Engl. J. Med. 352 (4): 351–61. 2005. doi:10.1056/NEJMoa041884. PMID 15673801.
- ^ Tobinick Edward L., Gross H, Weinberger A, Cohen H (2006). "TNF-alpha modulation for treatment of Alzheimer's disease: a 6-month pilot study". MedGenMed. 8 (2): 25. PMID 16926764.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Tobinick Edward L., Gross H. (2008). "Rapid cognitive improvement in Alzheimer's disease following perispinal etanercept administration". J. Neuroinflammation. 5 (2): 2. doi:10.1186/1742-2094-5-2. PMID 18184433.
{{cite journal}}: CS1 maint: unflagged free DOI (link)