Study of MLN8237 in Combination With Irinotecan and Temozolomide
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- New Approaches to Neuroblastoma Therapy Consortium
- Study ID
- NCT01601535
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 12 Months - 30 Years
- Healthy Volunteers
- Not accepted
Interventions
- MLN8237 — DRUGEvery course will be 21 days. MLN8237 will be administered orally daily starting on day 1 through day 7.
- Irinotecan — DRUGIrinotecan will be administered intravenously during each course on study day 1 through day 5.
- Temozolomide — DRUGTemozolomide will be administered orally during each course on study day 1 through day 5.
Study Details
The goal of the first part of this clinical trial (Phase I portion) is to study the side effects, drug breakdown (pharmacokinetics), and dosing of the drug MLN8237 when added to standard chemotherapy drugs, irinotecan and temozolomide. The goal of the second part of this clinical trial (Phase II portion) is to learn how many children and young adults show improvements in their neuroblastoma when treated with the combination of MLN8237, irinotecan, and temozolomide.
Key Dates
- Start date
- May 31, 2012
- Status verified
- Jul 2019
- Primary completion
- Jul 25, 2018
- Completion
- Jul 25, 2018
Study Design
- Enrollment
- 54 participants (actual)
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: TreatmentEvery course will be 21 days. MLN8237 will be administered orally daily starting on day 1 through day 7. Irinotecan will be administered intravenously during each course on study day 1 through day 5. Temozolomide will be administered orally during each course on study day 1 through day 5.
Primary Outcome Measure
Maximum Tolerated Dose (MTD) When Given Together With Fixed Doses of Irinotecan and Temozolomide in Children and Young Adults With Relapsed or Refractory Neuroblastoma [ Time Frame: 21 days, from study day 1 ]
Locations (12)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Children's Hospital Los Angeles | Los Angeles | California | 90027-0700 | - |
| Lucile Packard Children's Hospital at Stanford University Medical Center | Palo Alto | California | 94304 | - |
| UCSF Helen Diller Family Comprehensive Cancer Center | San Francisco | California | 94115 | - |
| Children Hospital of Colorado | Aurora | Colorado | 80045 | - |
| Children's Healthcare of Atlanta | Atlanta | Georgia | 30322 | - |
| University of Chicago Comer Children's Hospital | Chicago | Illinois | 60637 | - |
| Childrens Hospital Boston, Dana-Farber Cancer Institute. | Boston | Massachusetts | 02115 | - |
| University of Michigan Comprehensive Cancer Center | Ann Arbor | Michigan | 48109 | - |
| Cincinnati Children's Hospital Medical Center | Cincinnati | Ohio | 45229-3039 | - |
| Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | 19104-4318 | - |
| Cook Children's Medical Center - Fort Worth | Fort Worth | Texas | 76104 | - |
| Children's Hospital and Regional Medical Center - Seattle | Seattle | Washington | 98105 | - |
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Children's Hospital Los Angeles· Los Angeles, CALucile Packard Children's Hospital at Stanford University Medical Center· Palo Alto, CAUCSF Helen Diller Family Comprehensive Cancer Center· San Francisco, CAChildren Hospital of Colorado· Aurora, COChildren's Healthcare of Atlanta· Atlanta, GAUniversity of Chicago Comer Children's Hospital· Chicago, IL
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