Expanded Access for Idelalisib in Combination With Rituximab in Chronic Lymphocytic Leukemia
Part of paid clinical trials in La Jolla, California.
- Sponsor
- Gilead Sciences
- Study ID
- NCT02136511
- Status
- Approved For Marketing
Conditions
- Chronic Lymphocytic Leukemia (CLL)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Idelalisib — DRUGIdelalisib 150 mg tablet administered orally twice daily
- Rituximab — DRUGRituximab administered intravenously starting at 375 mg/m\^2 at Week 0 and continuing with a dose of 500 mg/m\^2 at Weeks 2, 4, 6, 8, 12, 16, and 20.
Study Details
This study is to provide idelalisib (IDELA) to individuals with relapsed, previously treated chronic lymphocytic leukemia (CLL) who have limited treatment options and are not eligible for other Gilead-sponsored studies.
Key Dates
- Status verified
- Oct 2014
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California, San Diego - Moores Cancer Center | La Jolla | California | 92093-0820 | - |
| Georgetown University | Washington D.C. | District of Columbia | 20007 | - |
| Hackensack University Medical Center | Hackensack | New Jersey | 07601 | - |
| Weill Cornell Medical College | New York | New York | 10021 | - |
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