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Plasma and cerebrospinal fluid pharmacokinetics of thalidomide and lenalidomide in nonhuman primates
Authors:Jodi?A.?Muscal,Yongkai?Sun,Jed?G.?Nuchtern,Robert?C.?Dauser,Leticia?H.?McGuffey,Brian?W.?Gibson,Stacey?L.?Berg  author-information"  >  author-information__contact u-icon-before"  >  mailto:sberg@txch.org"   title="  sberg@txch.org"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Texas Children’s Cancer Center, Baylor College of Medicine, 1102 Bates Street, Suite 1220, Houston, TX 77030, USA;(2) Celgene Corporation, Summit, NJ, USA;(3) Department of Surgery, Texas Children’s Hospital, Baylor College of Medicine, Houston, TX, USA;(4) Department of Neurosurgery, Texas Children’s Hospital, Baylor College of Medicine, Houston, TX, USA;(5) Center for Comparative Medicine, Baylor College of Medicine, Houston, TX, USA;
Abstract:

Purpose  

Thalidomide, originally developed as a sedative, was subsequently identified to have antiangiogenic properties. Lenalidomide is an antiangiogenic and immunomodulatory agent that has been utilized in the treatment of patients with brain tumors. We studied the pharmacokinetics and cerebrospinal fluid (CSF) penetration of thalidomide and lenalidomide in a nonhuman primate model.
Keywords:
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