A Study Of Ranpirnase(Onconase®) To Pemetrexed Plus Carboplatin In Patients With Non-Squamous Non-Small Cell Lung Cancer
Withdrawn before enrolling · Phase 2
Conditions studied: Non-Small Cell Lung Cancer
In brief
The purpose of the trial is to determine the rate of improvement in objective tumor response, following the addition of ranpirnase to ongoing pemetrexed-carboplatin chemotherapy, for patients with SD or PR following 2 cycles of doublet chemotherapy.
Key facts
- Study ID
- NCT01184287
- Run by
- Tamir Biotechnology, Inc.
- People needed
- 0
- Last updated by the study team
- 2015-09-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age greater than 18 years
- ECOG less than 2
- Estimated survival of greater than 12 weeks
You may not qualify if…
- Prior systemic chemotherapy for locally advanced or metastatic NSCLC
- Use of any investigational agent within 28 days prior to registration
- Known hypersensitivity to any of the study drugs
- Brain metastases or leptomeningeal disease
- History of prior malignancy within the past three years
Where it is running
- Tower Cancer Research Foundation — Beverly Hills, California, United States
- Van Andel Research Institute — Grand Rapids, Michigan, United States
- Sletten Cancer Specialists — Great Falls, Montana, United States
- The Cancer Institute at NYU Langone Medical Center — New York, New York, United States
- Tri-county Hematology-Oncology Associates, Inc — Canton, Ohio, United States
- Northern Utah Associates — Ogden, Utah, United States
Full record on ClinicalTrials.gov
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