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Brief Title: Safety Study of XL999 in Adults With Non-Small-Cell Lung Cancer
Official Title: A Phase 1 Dose Escalation Study of the Safety, Pharmacokinetics, and Pharmacodynamics of XL999 Administered Intravenously to Subjects With Non-Small-Cell Lung Cancer (NSCLC)
Study ID: NCT00491699
Brief Summary: The purpose of this study is to determine the safest dose of XL999 and how well subjects with Non-Small-Cell Lung Cancer tolerate XL999. XL999 is a small molecule inhibitor of multiple kinases including VEGFR, PDGFR, FGFR, FLT-3, and Src, which are involved in tumor cell growth, formation of new blood vessels (angiogenesis), and metastasis.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
UCLA Medical Center, Los Angeles, California, United States
Peachtree Hematology Oncology Consultants, Atlanta, Georgia, United States
Wayne State University, Karmanos Cancer Institute, Detroit, Michigan, United States
Hematology-Oncology Associates of Rockland, Nyack, New York, United States
Cancer Therapy and Research Center at The UT Health Science Center at San Antonio, San Antonio, Texas, United States
Name: Lynne A. Bui, MD
Affiliation: Exelixis
Role: STUDY_DIRECTOR