drugset / Trial / NCT00527982
Celecoxib as Adjuvant Biologic Therapy in Patients With Head and Neck and Lung Cancer
Phase 2
Terminated
1 enrolled
M.D. Anderson Cancer Center
United States Department of Defense · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
Primary Objectives: 1. To examine the effect of celecoxib treatment on histological response, markers of proliferation (Ki-67), and apoptosis. Secondary endpoints include time to second primary or recurrence and survival. 2. To examine the toxicity associated with celecoxib administration in patients with previously treated Head and Neck Head and neck squamous cell carcinomas (HNSCC)or Non-small-cell lung carcinoma (NSCLC).
Timeline
- Start
- 2005-09
- Primary completion
- 2008-09
- Completion
- 2008-09
Outcome
Outcome not reported
Stopped (Enrollment): “Termination due to poor accrual.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Celecoxib | Other / unclassified | 600 mg | Oral |