CompletedPhase 3NCT00035152

Study Comparing Weekly Taxol and Carboplatin vs Standard Taxol and Carboplatin Regimen for Stage IIIB or IV Non-Small-Cell Lung Cancer

Taxol and carboplatin are commonly used drugs for the treatment of stage IIIB or IV non small cell lung carcinoma. This study compares treatment with Taxol/carboplatin given every 3 weeks to a schedule where it is given weekly. The purpose of the study is to determine the most effective and safe schedule for giving these drugs in non small cell lung carcinoma.

Checked against the public recordLast updated Sep 19, 2016 · Source: ClinicalTrials.gov

StatusCompleted
PhasePhase 3
U.S. locations56
SponsorBristol-Myers Squibb
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 3
Sponsor
Bristol-Myers Squibb
Interventions being studied
Drug: Paclitaxel and carboplatin
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion criteria: * Confirmation of non-small cell bronchogenic carcinoma (epidermoid, squamous, adeno, large cell anaplastic carcinoma, but no small cell or carcinoid) must be histologically or cytologically confirmed. * No prior antineoplastic chemotherapy, hormonal therapy or therapy with biological response modifiers * No previous irradiation to the only area of measurable disease. Exclusion Criteria: * Past or current history of neoplasm other than the entry diagnosis. Exceptions are curatively treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix or other cancers treated by surgery or radiation with a disease free survival longer than 5 years. * Patients who have undergone surgery less than 3 weeks prior to enrollment. * History of serious cardiac disease not adequately controlled. * Patients with serious active infections or other serious underlying medical condition. * Uncontrolled diabetes mellitis.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Genesis Cancer CenterHot Springs, Arkansas
  • Little Rock Hematology/Oncology AssociatesLittle Rock, Arkansas
  • Highlands Oncology GroupSpringdale, Arkansas
  • Medical Oncology Care AssociatesOrange, California
  • Naval Medical CenterSan Diego, California
  • Danbury Hospital/Praxair Cancer CenterDanbury, Connecticut
  • Walter Reed Army HospitalWashington D.C., District of Columbia
  • Washington VA Medical CenterWashington D.C., District of Columbia
  • Good Samaritan Medical CenterWest Palm Beach, Florida
  • Wellstar Cobb HospitalAustell, Georgia
  • Joliet Oncology/Hematology Associates,Ltd.Joliet, Illinois
  • Mid Illinois Hematology and Oncology Associates, Ltd.Normal, Illinois

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Sep 19, 2016. Always confirm current availability with the study team.

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