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NCT00698815 · ClinicalTrials.gov registry record · Phase 2
Pemetrexed and/or Sunitinib as Second-Line Therapy in Treating Patients With Stage IIIB or Stage IV Non-small Cell Lung Cancer
A Phase 2 study of Recurrent Non-Small Cell Lung Carcinoma and Stage IV Non-Small Cell Lung Cancer AJCC v7, sponsored by National Cancer Institute (NCI).
- Completed
- Registry status
- Phase 2
- Development phase
- 130
- Enrollment target
- 20
- Study locations
NCT00698815: Completed Phase 2 study of Recurrent Non-Small Cell Lung Carcinoma and Stage IV Non-Small Cell Lung Cancer AJCC v7, sponsored by National Cancer Institute (NCI).
NCT00698815 is a Phase 2 study of Recurrent Non-Small Cell Lung Carcinoma and Stage IV Non-Small Cell Lung Cancer AJCC v7 that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 130 participants, above the 105-participant average among 6 other Recurrent Non-Small Cell Lung Carcinoma trials with a reported enrollment target (24% higher). The trial reports 20 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00698815, a Phase 2 study of Recurrent Non-Small Cell Lung Carcinoma and Stage IV Non-Small Cell Lung Cancer AJCC v7, has completed, sponsored by National Cancer Institute (NCI).
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 130 participants
- Enrollment target
- 20
- Study locations
Study Summary
This randomized phase II trial studies pemetrexed disodium and sunitinib malate to compare how well they work when given alone or together as second-line therapy in treating patients with stage IIIB or stage IV non-small cell lung cancer. Drugs used in chemotherapy, such as pemetrexed disodium, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Sunitinib malate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. It is not yet known whether pemetrexed disodium and sunitinib malate are more effective when given alone or together in treating non-small cell lung cancer.
Primary Outcome
The 18 week progression-free survival rate was defined as the proportion of patients that were alive and progression-free 18 weeks after registration into the study. Disease progression was assessed per modified RECIST criteria, and defined as at least a 20% increase in the sum of the longest diameters of target lesions, in either primary or nodal lesions, taking as reference the smallest sum longest diameter recorded since the baseline measurements, or the appearance of new lesions. Kaplan-Meie
Conditions Studied
Interventions
- OTHER Laboratory Biomarker Analysis
- DRUG Pemetrexed Disodium
- DRUG Sunitinib Malate
Study Locations (20)
California
- Kaiser Permanente-Anaheim - Anaheim
- Arroyo Grande Community - Arroyo Grande
- Kaiser Permanente-Baldwin Park - Baldwin Park
- Kaiser Permanente-Bellflower - Bellflower
- East Bay Radiation Oncology Center - Castro Valley
- Eden Hospital Medical Center - Castro Valley
- Valley Medical Oncology Consultants-Castro Valley - Castro Valley
- Bay Area Breast Surgeons Inc - Emeryville
- Kaiser Permanente Hospital - Fontana
- Valley Medical Oncology Consultants-Fremont - Fremont
- Kaiser Permanente - Harbor City - Harbor City
- Kaiser Permanente-Irvine - Irvine
- Kaiser Permanente Los Angeles Medical Center - Los Angeles
- Kaiser Permanente-Cadillac - Los Angeles
- Contra Costa Regional Medical Center - Martinez
- El Camino Hospital - Mountain View
- Highland General Hospital - Oakland
- Alta Bates Summit Medical Center - Summit Campus - Oakland
- Bay Area Tumor Institute - Oakland
- Hematology and Oncology Associates-Oakland - Oakland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 130 participants |
| Start Date | 2008-04-15 |
| Phase | Phase 2 |
What the finished NCT00698815 record still lists
NCT00698815 is an interventional study that assigns participants to a tested intervention. The registered 130 participants enrollment target is mid-sized for trials with a published cap, above the 105-participant average among 6 other Recurrent Non-Small Cell Lung Carcinoma trials with a reported enrollment target (24% higher).
The record links to 3 conditions, with Recurrent Non-Small Cell Lung Carcinoma appearing as the primary indexed condition, and to 3 interventions - of which Laboratory Biomarker Analysis is the first listed.
NCT00698815 names 20 study sites across 1 states, led by California.
Frequently Asked Questions
What is clinical trial NCT00698815 about?
NCT00698815 is a clinical study titled "Pemetrexed and/or Sunitinib as Second-Line Therapy in Treating Patients With Stage IIIB or Stage IV Non-small Cell Lung Cancer". This randomized phase II trial studies pemetrexed disodium and sunitinib malate to compare how well they work when given alone or together as second-line therapy in treating patients with stage IIIB or stage IV non-small cell lung cancer. Drugs used in chemotherapy, such as pemetrexed disodium, work...
What is the current status of trial NCT00698815?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 130 participants. The study started on 2008-04-15.
What conditions does trial NCT00698815 study?
This clinical trial studies the following conditions: Recurrent Non-Small Cell Lung Carcinoma, Stage IV Non-Small Cell Lung Cancer AJCC v7, Stage IIIB Non-Small Cell Lung Cancer AJCC v7.
What interventions are being tested in trial NCT00698815?
The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Pemetrexed Disodium (DRUG), Sunitinib Malate (DRUG).
Who is sponsoring clinical trial NCT00698815?
This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00698815 being conducted?
This trial has 20 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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