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Spots Global Cancer Trial Database for Study of XL281 in Adults With Solid Tumors

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Study of XL281 in Adults With Solid Tumors

Official Title: A Phase 1 Dose-Escalation Study of the Safety and Pharmacokinetics of XL281 Administered Orally to Subjects With Solid Tumors

Study ID: NCT00451880

Interventions

XL281
famotidine

Study Description

Brief Summary: The purpose of this study is to determine the safest dose of the multiple Raf kinase inhibitor (including c-Raf, B-Raf, and the activated mutant B-RafV600E) XL281, how often it should be taken, and how well subjects with cancer tolerate XL281. This study will also determine how the body reacts to XL281 when it is taken with and without food, and with and without Pepcid (famotidine), a drug that inhibits stomach acid production.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Premiere Oncology of Arizona, Scottsdale, Arizona, United States

H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States

Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

Mary Crowley Cancer Research Center, Dallas, Texas, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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