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Sponsored by: |
Exelixis |
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Information provided by: | Exelixis |
ClinicalTrials.gov Identifier: | NCT00350831 |
The purpose of this study is to assess the safety and tolerability of the KIT inhibitor XL820 when given orally daily to adults with advanced solid tumors.
Condition | Intervention | Phase |
---|---|---|
Cancer |
Drug: XL820 |
Phase I |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety Study |
Official Title: | A Phase 1 Dose Escalation Study of the Safety and Pharmacokinetics of the KIT Inhibitor XL820 Administered Orally Daily to Subjects With Solid Tumors |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, New Jersey | |
The Cancer Institute of New Jersey | |
New Brunswick, New Jersey, United States, 08901 | |
United States, Texas | |
Cancer Therapy and Research Center | |
San Antonio, Texas, United States, 78229 |
Study ID Numbers: | XL820-002 |
Study First Received: | July 7, 2006 |
Last Updated: | August 14, 2008 |
ClinicalTrials.gov Identifier: | NCT00350831 |
Health Authority: | United States: Food and Drug Administration |
Solid tumor |