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Gemcitabine and Epirubicin in Treating Patients With Malignant Mesothelioma
NCT00017186 · 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 tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining gemcitabine and epirubicin in treating patients who have malignant mesothelioma.
Conditions Studied
Interventions
- DRUG epirubicin hydrochloride
- DRUG gemcitabine hydrochloride
Study Locations (20)
Minnesota
- CCOP - Duluth — Duluth
- Mayo Clinic Cancer Center — Rochester
- Coborn Cancer Center — Saint Cloud
- CCOP - Metro-Minnesota — Saint Louis Park
Iowa
- CCOP - Cedar Rapids Oncology Project — Cedar Rapids
- CCOP - Iowa Oncology Research Association — Des Moines
- Siouxland Hematology-Oncology — Sioux City
Illinois
- CCOP - Illinois Oncology Research Association — Peoria
- CCOP - Carle Cancer Center — Urbana
North Dakota
- Medcenter One Health System — Bismarck
- CCOP - Merit Care Hospital — Fargo
Alabama
- MBCCOP - Gulf Coast — Mobile
Arizona
- CCOP - Mayo Clinic Scottsdale Oncology Program — Scottsdale
Florida
- Mayo Clinic - Jacksonville — Jacksonville
Kansas
- CCOP - Wichita — Wichita
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 69 participants |
| Start Date | 2001-07 |
| Est. Completion | 2008-05 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00017186
The ClinicalTrials.gov registry entry for NCT00017186 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. The registered enrollment target is 69 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alliance for Clinical Trials in Oncology, which has 147 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 Malignant Mesothelioma appearing as the primary indexed condition, and to 2 interventions — of which epirubicin hydrochloride 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: NCT00017186 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Minnesota, Iowa, Illinois. 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 NCT00017186 about?
NCT00017186 is a clinical study titled "Gemcitabine and Epirubicin in Treating Patients With Malignant Mesothelioma". 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 tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining gemcitabine and epirubicin in treating patients who have ma...
What is the current status of trial NCT00017186?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 69 participants. The study started on 2001-07. Estimated completion is 2008-05.
What conditions does trial NCT00017186 study?
This clinical trial studies the following conditions: Malignant Mesothelioma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00017186?
The interventions under investigation include: epirubicin hydrochloride (DRUG), gemcitabine hydrochloride (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00017186?
This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 147 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00017186 being conducted?
This trial has 20 study locations across Alabama, Arizona, Florida, Illinois, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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