Ustekinumab: Difference between revisions
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==Mechanism of action== |
==Mechanism of action== |
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CNTO 1275 is designed to interfere with the triggering of the body's [[Inflammation|inflamatory response]] through the suppression of certain [[cytokines]]. Specifically, CNTO 1275 blocks [[interleukin]] [[IL-12]] and [[IL-23]] which help activiate certain [[T cell|T-cells]]. |
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==References== |
==References== |
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Revision as of 02:30, 4 August 2008
| Monoclonal antibody | |
|---|---|
| Type | ? |
| Source | Human |
| Target | IL-12 and IL-23 |
| Clinical data | |
| Routes of administration | Subcutaneous injection |
| ATC code | |
| Legal status | |
| Legal status |
|
| Identifiers | |
| CAS Number | |
| Chemical and physical data | |
| Formula | C6482H10004N1712O2016S46 |
| Molar mass | 145.64 kDa g·mol−1 |
Ustekinumab (INN, experimental name CNTO 1275) is a human immunosuppressive drug developed by the biotechnology company Centocor. It is a laboratory-manufactured monoclonal antibody directed against interleukins IL-12 and IL-23.[1] Ustekinumab is presently undergoing clinical trials to determine its safety and effectiveness against multiple sclerosis, psoriasis, and psoriatic arthritis. The results of Phase III trials for psoriasis have been encouraging; two large randomized controlled trials, one conducted over 76 weeks and the other over a year, showed ustekinumab to be safe and effective for moderate to severe psoriasis.[2][3]
Development
As of January 2007, there were 5 NIH-listed research studies involving CNTO 1275 on a multinational basis, including 3 Phase II and 2 Phase III trials. Three studies are focused on patients with psoriasis, one on psoriatic arthritis, and one on multiple sclerosis.
On December 4, 2007, a Biologics License Application (BLA) with the U.S. Food and Drug Administration (FDA) was filed by Centocor and Janssen-Cilag International (collaborator) has submitted a Marketing Authorization Application (MAA) to the European Medicines Agency (EMEA).
On June 17, 2008, the Dermatologic and Ophthalmic Drugs Advisory Committee (DODAC) of the U.S. Food and Drug Administration unanimously recommended the approval of ustekinumab (CNTO 1275) for the treatment of adult patients with moderate to severe plaque psoriasis. The decision by the committee is non-binding and final decisions on approval of the drug are made by the FDA. As yet, there is no schedule for when the FDA will make a decision on CNTO 1275.
Delivery
Patients enrolled in clinical trials of CNTO 1275 are scheduled to receive the drug by subcutaneous injections at doses of either 45 or 90 mg. The dosage and frequency varies by study and application (type of disease targeted). Generally the initial dosing interval is once per week followed by a step-down to once per month or even once every three months.
Mechanism of action
CNTO 1275 is designed to interfere with the triggering of the body's inflamatory response through the suppression of certain cytokines. Specifically, CNTO 1275 blocks interleukin IL-12 and IL-23 which help activiate certain T-cells.
References
- ^ Reddy M, Davis C, Wong J, Marsters P, Pendley C, Prabhakar U (2007). "Modulation of CLA, IL-12R, CD40L, and IL-2Ralpha expression and inhibition of IL-12- and IL-23-induced cytokine secretion by CNTO 1275". Cell. Immunol. 247 (1): 1–11. doi:10.1016/j.cellimm.2007.06.006. PMID 17761156.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ Leonardi CL, Kimball AB, Papp KA; et al. (2008). "Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 76-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 1)". Lancet. 371 (9625): 1665–74. doi:10.1016/S0140-6736(08)60725-4. PMID 18486739.
{{cite journal}}: Explicit use of et al. in:|author=(help); Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ Papp KA, Langley RG, Lebwohl M; et al. (2008). "Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 52-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 2)". Lancet. 371 (9625): 1675–84. doi:10.1016/S0140-6736(08)60726-6. PMID 18486740.
{{cite journal}}: Explicit use of et al. in:|author=(help); Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link)
External links
- CNTO 1275 research studies registered with U.S. National Institutes of Health:
- Sylvester, Bruce (2006-03-06). "CNTO 1275 Shows Efficacy for Psoriasis: Presented at AAD". Doctor's Guide Publishing. Retrieved 2007-01-25.