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http://linked.open...gbank/description
| - Brentuximag vedotin or Adcetris® is an antibody-drug conjugate that combines an anti-CD30 antibody and the drug monomethyl auristatin E (MMAE). It is an anti-neoplastic agent used in the treatment of Hodgkin lymphoma and systemic anaplastic large cell lymphoma. Brentuximag vedotin was approved in 2011, and in January 2012, the drug label was revised to include a boxed warning of progressive multifocal leukoencephalopathy and death following JC virus infection. (en)
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http://linked.open...y/drugbank/dosage
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http://linked.open...generalReferences
| - # Francisco JA, Cerveny CG, Meyer DL, Mixan BJ, Klussman K, Chace DF, Rejniak SX, Gordon KA, DeBlanc R, Toki BE, Law CL, Doronina SO, Siegall CB, Senter PD, Wahl AF: cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity. Blood. 2003 Aug 15;102(4):1458-65. Epub 2003 Apr 24. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/12714494 (en)
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http://linked.open...gy/drugbank/group
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http://linked.open...drugbank/halfLife
| - The terminal half-life is 4-6 days. (en)
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http://linked.open...ugbank/indication
| - Used in the treatment of Hodgkin lymphoma and systemic anaplastic large cell lymphoma. (en)
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Title
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adms:identifier
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http://linked.open...mechanismOfAction
| - Brentuximab vedotin is composed of 3 parts: a chimeric human-murine IgG1 that targets CD30, monomethyl auristatin E (MMAE),which is a microtubule disrupting agent, and a protease-susceptible linker that covalently links the antibody and MMAE. The IgG1 antibody enables brentuximab vedotin to target tumor cells expressing CD30 on their cell surface then brentuximab vedotin gets internalized into the cell. Once inside, the linker is cleaved releasing MMAE which binds disrupts the microtuble network. (en)
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http://linked.open...outeOfElimination
| - MMAE is eliminated by the feces (with 72% unchanged) and urine. (en)
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http://linked.open.../drugbank/synonym
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http://linked.open...drugbank/toxicity
| - The most severe toxic reaction seen in patients is progressive multifocal leukoencephalopathy. Other toxicities include bone marrow suppression, infusion reactions, peripheral neuropathy, Stevens-Johnson syndrome, and tumor lysis syndrome. (en)
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http://linked.open...umeOfDistribution
| - The steady state volume of distribution is 6-10 L. (en)
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http://linked.open...nk/proteinBinding
| - MMAE has a plasma protein binding range of 68-82%, and highly-protein bound drugs are not likely to displace it. (en)
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http://linked.open...ynthesisReference
| - Francisco JA, Cerveny CG, Meyer DL, Mixan BJ, Klussman K, Chace DF, Rejniak SX, Gordon KA, DeBlanc R, Toki BE, Law CL, Doronina SO, Siegall CB, Senter PD, Wahl AF: cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity. Blood. 2003 Aug 15;102(4):1458-65. Epub 2003 Apr 24 (en)
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foaf:page
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http://linked.open...Molecular-Formula
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http://linked.open.../Molecular-Weight
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http://linked.open...l/drug/hasATCCode
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http://linked.open...ugbank/absorption
| - Brentuximab vedotin is administered only as an intravenous infusion so absorption is 100%. (en)
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http://linked.open.../affectedOrganism
| - Humans and other mammals (en)
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http://linked.open...casRegistryNumber
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http://linked.open...rugbank/clearance
| - MMAE is cleared by the liver but not quantitative studies have been performed. (en)
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