ClinicalTrials.gov record
Completed Phase 2 Interventional

Gemcitabine and Epirubicin in Treating Patients With Malignant Mesothelioma

ClinicalTrials.gov ID: NCT00017186

Public ClinicalTrials.gov record NCT00017186. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 4, 2026, 11:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Study of Gemcitabine and Epirubicin for the Treatment of Mesothelioma

Study identification

NCT ID
NCT00017186
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alliance for Clinical Trials in Oncology
Other
Enrollment
69 participants

Conditions and interventions

Interventions

  • epirubicin hydrochloride Drug
  • gemcitabine hydrochloride Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2001
Primary completion
Jul 31, 2004
Completion
Apr 30, 2008
Last update posted
Dec 6, 2016

2001 – 2008

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
MBCCOP - Gulf Coast Mobile Alabama 36607
CCOP - Mayo Clinic Scottsdale Oncology Program Scottsdale Arizona 85259-5404
Mayo Clinic - Jacksonville Jacksonville Florida 32224
CCOP - Illinois Oncology Research Association Peoria Illinois 61602
CCOP - Carle Cancer Center Urbana Illinois 61801
CCOP - Cedar Rapids Oncology Project Cedar Rapids Iowa 52403-1206
CCOP - Iowa Oncology Research Association Des Moines Iowa 50309-1016
Siouxland Hematology-Oncology Sioux City Iowa 51101-1733
CCOP - Wichita Wichita Kansas 67214-3882
CCOP - Ochsner New Orleans Louisiana 70121
CCOP - Michigan Cancer Research Consortium Ann Arbor Michigan 48106
CCOP - Duluth Duluth Minnesota 55805
Mayo Clinic Cancer Center Rochester Minnesota 55905
Coborn Cancer Center Saint Cloud Minnesota 56303
CCOP - Metro-Minnesota Saint Louis Park Minnesota 55416
CCOP - Missouri Valley Cancer Consortium Omaha Nebraska 68106
Medcenter One Health System Bismarck North Dakota 58501-5505
CCOP - Merit Care Hospital Fargo North Dakota 58122
CCOP - Toledo Community Hospital Toledo Ohio 43623-3456
CCOP - Geisinger Clinic and Medical Center Danville Pennsylvania 17822-2001
CCOP - Upstate Carolina Spartanburg South Carolina 29303
Rapid City Regional Hospital Rapid City South Dakota 57709
CCOP - Sioux Community Cancer Consortium Sioux Falls South Dakota 57104
CCOP - St. Vincent Hospital Cancer Center, Green Bay Green Bay Wisconsin 54301

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00017186, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 6, 2016 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00017186 live on ClinicalTrials.gov.

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