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| C=502 | H=758 | N=154 | O=165 | S=16 | | C=502 | H=758 | N=154 | O=165 | S=16 | ||
| molecular_weight = 12,103 g/mol (protein part) | |||
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'''Pegsunercept''' is a ] for the treatment of ]. {{As of|2010|1}}, Phase II ]s have been completed.<ref>{{ClinicalTrialsGov|NCT00037700|Evaluation of the Efficacy of Combination Treatment With Anakinra and Pegsunercept in Improving Rheumatoid Arthritis}}</ref><ref>{{ClinicalTrialsGov|NCT00111423|Evaluating the Safety of Extended Treatment With Pegsunercept (PEG sTNF-RI)in Subjects With Rheumatoid Arthritis (RA)}}</ref><ref name="Furst">{{cite journal | vauthors = Furst DE, Fleischmann R, Kopp E, Schiff M, Edwards C, Solinger A, Macri M | title = A phase 2 dose-finding study of PEGylated recombinant methionyl human soluble tumor necrosis factor type I in patients with rheumatoid arthritis | journal = The Journal of Rheumatology | volume = 32 | issue = 12 | pages = 2303–10 | date = December 2005 | pmid = 16331754 }}</ref> It is being developed by ]. | '''Pegsunercept''' is a ] for the treatment of ]. {{As of|2010|1}}, Phase II ]s have been completed.<ref>{{ClinicalTrialsGov|NCT00037700|Evaluation of the Efficacy of Combination Treatment With Anakinra and Pegsunercept in Improving Rheumatoid Arthritis}}</ref><ref>{{ClinicalTrialsGov|NCT00111423|Evaluating the Safety of Extended Treatment With Pegsunercept (PEG sTNF-RI)in Subjects With Rheumatoid Arthritis (RA)}}</ref><ref name="Furst">{{cite journal | vauthors = Furst DE, Fleischmann R, Kopp E, Schiff M, Edwards C, Solinger A, Macri M | title = A phase 2 dose-finding study of PEGylated recombinant methionyl human soluble tumor necrosis factor type I in patients with rheumatoid arthritis | journal = The Journal of Rheumatology | volume = 32 | issue = 12 | pages = 2303–10 | date = December 2005 | pmid = 16331754 }}</ref> It is being developed by ]. |
Latest revision as of 06:59, 31 December 2023
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Routes of administration | subcutaneous injection |
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Bioavailability | N/A |
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Formula | C502H758N154O165S16 |
Molar mass | 12103.46 g·mol |
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Pegsunercept is a drug for the treatment of rheumatoid arthritis. As of January 2010, Phase II clinical trials have been completed. It is being developed by Amgen.
Similarly to etanercept, pegsunercept is a soluble tumor necrosis factor receptor. Pegsunercept is a PEGylated protein.
References
- Clinical trial number NCT00037700 for "Evaluation of the Efficacy of Combination Treatment With Anakinra and Pegsunercept in Improving Rheumatoid Arthritis" at ClinicalTrials.gov
- Clinical trial number NCT00111423 for "Evaluating the Safety of Extended Treatment With Pegsunercept (PEG sTNF-RI)in Subjects With Rheumatoid Arthritis (RA)" at ClinicalTrials.gov
- ^ Furst DE, Fleischmann R, Kopp E, Schiff M, Edwards C, Solinger A, Macri M (December 2005). "A phase 2 dose-finding study of PEGylated recombinant methionyl human soluble tumor necrosis factor type I in patients with rheumatoid arthritis". The Journal of Rheumatology. 32 (12): 2303–10. PMID 16331754.
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