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Brief Title: Study of XL999 in Adults With Solid Tumors
Official Title: A Phase 1 Dose Escalation Study of the Safety, Pharmacokinetics, and Pharmacodynamics of XL999 Administered Intravenously to Subjects With Solid Tumors
Study ID: NCT00104117
Brief Summary: The purpose of this study is to assess the safety and tolerability of XL999 in adults with advanced solid tumors.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Case Western Reserve University, Univserzity Hospitals of Cleveland, Cleveland, Ohio, United States
Cancer Therapy and Research Center, Institute for Drug Development, San Antonio, Texas, United States
Name: Paul Woodard, MD
Affiliation: Exelixis
Role: STUDY_DIRECTOR