Irinotecan for Previously Treated, Advanced, Non-Small Cell Lung Cancer
Part of paid clinical trials in Albuquerque, New Mexico.
- Sponsor
- New Mexico Cancer Research Alliance
- Study ID
- NCT01607554
- Phase
- PHASE1/PHASE2
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Irinotecan — DRUG180 mg/m2 Irinotecan intravenously over 60 minutes on day 1 of each cycle Pre-medication for irinotecan: palonosetron 0.25 mg and dexamethasone 8 - 16 mg, both administered intravenously. Atropine 0.25 - 0.5 mg subcutaneously or IV is at the discretion of the treating physician
Study Details
Certain genetic factors can affect a patient's potential sensitivity to therapeutic drugs and other agents. There is a factor called ISG15 which might help doctors better identify patients with advanced non-small cell lung cancer (NSCLC) whose tumors may be more sensitive to the drug called Irinotecan. This factor is elevated in roughly 30% of NSCLC cases. Irinotecan is an agent that inhibits the enzyme called topoisomerase I that is involved in cell growth, and it has been FDA approved for 17 years for another type of cancer.
Key Dates
- Start date
- Apr 30, 2012
- Status verified
- Mar 2018
- Primary completion
- Mar 31, 2013
- Completion
- Mar 31, 2013
Study Design
- Enrollment
- 2 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: IrinotecanThe starting dose of irinotecan for the study is 180 mg/m2, given intravenously every 14 days. Each 14 day period will constitute one cycle of treatment.
Primary Outcome Measure
Tumor Response [ Time Frame: 8 weeks ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Hematology Oncology Associates | Albuquerque | New Mexico | 87106 | - |
| University of New Mexico Cancer Center | Albuquerque | New Mexico | 87131 | - |
| New Mexico Cancer Care Associates | Santa Fe | New Mexico | 87505 | - |
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