Urelumab
| Identyfikacja | |
| Inne nazwy i oznaczenia |
BMS-663513, Anti-CD137 |
|---|---|
| Genetyka i fizjologia | |
| Typ białka |
przeciwciała monoklonalne |
| Uwagi terapeutyczne | |
| Drogi podawania | |
Urelumab – lek biologiczny, ludzkie przeciwciała monoklonalne skierowane przeciwko receptorowi immunoregulatorowemu CD-137 (jeden z receptorów czynnika martwicy nowotworu, TNF). Stymulacja CD-137 zwiększa odpowiedź immunologiczną organizmu a szczególnie odpowiedź przeciwko komórkom nowotworowym.[1] Cząsteczka jest obecnie w drugiej fazie badań klinicznych.
Przypisy
- ↑ A. Molckovsky, LL. Siu. First-in-class, first-in-human phase I results of targeted agents: highlights of the 2008 American society of clinical oncology meeting.. „J Hematol Oncol”. 1, s. 20, 2008. DOI: 10.1186/1756-8722-1-20. PMID: 18959794.
Bibliografia
- A. Tomillero, MA. Moral. Gateways to clinical trials.. „Methods Find Exp Clin Pharmacol”. 30 (7), s. 543-88, Sep 2008. PMID: 18985183.
Linki zewnętrzne
- Badania kliniczne
- Safety, Tolerability, Pharmacokinetics, and Immunoregulatory Study of BMS-663513 in Subjects With Advanced and/or Metastatic Solid Tumors, [w:] ClinicalTrials.gov [online], National Institutes of Health, NCT01471210 (ang.).
- Phase II, 2nd Line Melanoma – RAND Monotherapy, [w:] ClinicalTrials.gov [online], National Institutes of Health, NCT00612664 (ang.).
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