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Spots Global Cancer Trial Database for Safety Study of Pharmacokinetics of XL888 in Adults With Solid Tumors

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Trial Identification

Brief Title: Safety Study of Pharmacokinetics of XL888 in Adults With Solid Tumors

Official Title: A Phase 1 Dose-Escalation Study of the Safety and Pharmacokinetics of XL888 in Subjects With Solid Tumors

Study ID: NCT00796484

Conditions

Cancer

Interventions

XL888

Study Description

Brief Summary: The purpose of this study is to evaluate the safety and tolerability of XL888 in subjects with solid tumors. XL888 is a potent and selective inhibitor of HSP90, a key component of a molecular chaperone complex that promotes the conformational maturation and stabilization of diverse client proteins. Many HSP90 client proteins play critical roles in signaling pathways implicated in tumor cell growth, proliferation, and survival.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Hospital of the University of Pennsylvania Abramson Cancer Center, Philadelphia, Pennsylvania, United States

South Texas Accelerated Research Therapeutics, San Antonio, Texas, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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