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Irinotecan and Docetaxel in Treating Patients With Metastatic or Locally Recurrent Head and Neck Cancer
NCT00040807 · View on ClinicalTrials.gov ↗
Study Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of irinotecan and docetaxel in treating patients who have metastatic or locally recurrent head and neck cancer.
Conditions Studied
Interventions
- DRUG docetaxel
- DRUG irinotecan hydrochloride
Study Locations (20)
Colorado
- Medical Center of Aurora - South Campus — Aurora
- Boulder Community Hospital — Boulder
- Penrose Cancer Center — Colorado Springs
- Porter Adventist Hospital — Denver
- St. Joseph Hospital — Denver
- Presbyterian - St. Luke's Medical Center — Denver
- Rocky Mountain Cancer Centers - Denver Rose — Denver
- CCOP - Colorado Cancer Research Program, Incorporated — Denver
- Swedish Medical Center — Englewood
- Sky Ridge Medical Center — Lone Tree
- Hope Cancer Care Center at Longmont United Hospital — Longmont
- St. Mary-Corwin Regional Medical Center — Pueblo
- Rocky Mountain Cancer Centers - Thornton — Thornton
Illinois
- Veterans Affairs Medical Center - Lakeside Chicago — Chicago
- Robert H. Lurie Comprehensive Cancer Center at Northwestern University — Chicago
Alabama
- University of Alabama at Birmingham Comprehensive Cancer Center — Birmingham
California
- Stanford Cancer Center at Stanford University Medical Center — Stanford
Delaware
- CCOP - Christiana Care Health Services — Newark
Florida
- H. Lee Moffitt Cancer Center and Research Institute — Tampa
Georgia
- Veterans Affairs Medical Center - Atlanta (Decatur) — Decatur
Trial Details
| Field | Value |
|---|---|
| Start Date | 2002-11-19 |
| Est. Completion | 2009-05-01 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00040807
The ClinicalTrials.gov registry entry for NCT00040807 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. An enrollment target was not published in the registry record, which is common for early-stage or observational entries. The listed sponsor is Eastern Cooperative Oncology Group, which has 30 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Head and Neck Cancer appearing as the primary indexed condition, and to 2 interventions — of which docetaxel is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00040807 reports 20 study locations spanning 7 distinct geographic areas — top geographies include Colorado, Illinois, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00040807 about?
NCT00040807 is a clinical study titled "Irinotecan and Docetaxel in Treating Patients With Metastatic or Locally Recurrent Head and Neck Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of irinotecan and docetaxel in treating patients who have metastatic or...
What is the current status of trial NCT00040807?
This trial is currently completed. It is a Phase 2 study. The study started on 2002-11-19. Estimated completion is 2009-05-01.
What conditions does trial NCT00040807 study?
This clinical trial studies the following conditions: Head and Neck Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00040807?
The interventions under investigation include: docetaxel (DRUG), irinotecan hydrochloride (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00040807?
This trial is sponsored by Eastern Cooperative Oncology Group, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00040807 being conducted?
This trial has 20 study locations across Alabama, California, Colorado, Delaware, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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