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F r o m W i k i p e d i a , t h e f r e e e n c y c l o p e d i a
Lumiliximab is an IgG1k monoclonal antibody that targets CD23 . It acts as an immunomodulator [1] and was awarded orphan drug status and fast track designation by the FDA.[2]
It was investigated in Phase II/III clinical trials for the treatment of chronic lymphocytic leukemia .[3] [4] It has also been studied for use in allergic asthma . The drug is a chimeric antibody from Macaca irus and Homo sapiens .[1]
Lumiliximab was developed by IDEC Pharmaceuticals, which was acquired by Biogen .
Clinical trials for CLL were terminated in 2010, and for allergic asthma in 2007.[2] Results published from the CLL clinical trial failed to meet primary endpoints.[5]
References
[ edit ]
^ Byrd JC, Kipps TJ, Flinn IW, Castro J, Lin TS, Wierda W, et al. (January 2010). "Phase 1/2 study of lumiliximab combined with fludarabine, cyclophosphamide, and rituximab in patients with relapsed or refractory chronic lymphocytic leukemia" . Blood . 115 (3 ): 489–95. doi :10.1182/blood-2009-08-237727 . PMC 2810983 . PMID 19843887 .
^ Clinical trial number NCT00801060 for "Evaluation of Safety and Efficacy of Fludarabine, Cyclophosphamide, and Rituximab (FCR) +/- Lumiliximab in Subjects With Previously Untreated Chronic Lymphocytic Leukemia (CLL)" at ClinicalTrials.gov
^ Awan FT, Hillmen P, Hellmann A, Robak T, Hughes SG, Trone D, et al. (November 2014). "A randomized, open-label, multicentre, phase 2/3 study to evaluate the safety and efficacy of lumiliximab in combination with fludarabine, cyclophosphamide and rituximab versus fludarabine, cyclophosphamide and rituximab alone in subjects with relapsed chronic lymphocytic leukaemia" . British Journal of Haematology . 167 (4 ): 466–77. doi :10.1111/bjh.13061 . hdl :2318/1577053 . PMID 25130401 . S2CID 25789983 .
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R e t r i e v e d f r o m " https://en.wikipedia.org/w/index.php?title=Lumiliximab&oldid=1193763495 "
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