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COMPLETED Phase 2

A Phase II Study of Epothilone Analog BMS-247550 in Patients With Non-Small Cell Lung Cancer Who Have Failed First Line Platinum Based Chemotherapy

NCT00035516 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this clinical research study is to learn if BMS-247550 can shrink or slow the growth of the cancer in patients with non-small cell lung cancer who have failed first-line platinum based chemotherapy. The safety of this treatment will also be studied.

Interventions

  • DRUG Epothilone

Study Locations (16)

Florida

  • Mount Sinai Medical Center — Miami Beach
  • H Lee Moffitt Cancer Center — Tampa

Tennessee

  • Sarah Cannon Cancer Center — Nashville
  • Vanderbilt University Med School Div of Medical Oncology — Nashville

Alabama

  • University of Alabama at Birmingham — Birmingham

California

  • Un of California Davis Cancer Center — Sacramento

Illinois

  • Rush Presbyterian St Lukes ME — Chicago

Kentucky

  • Consultants in Blood Disorders — Louisville

Louisiana

  • Ochsner Cancer Institute — New Orleans

Maryland

  • University of Maryland Greenbaum Cancer Center — Baltimore

Trial Details

FieldValue
Start Date 2001-02
Est. Completion 2004-04
Phase Phase 2

Sponsor

R-Pharm

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00035516

The ClinicalTrials.gov registry entry for NCT00035516 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 R-Pharm, which has 7 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 Carcinoma, Non-small-cell Lung appearing as the primary indexed condition, and to 1 intervention — of which Epothilone 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: NCT00035516 reports 16 study locations spanning 14 distinct geographic areas — top geographies include Florida, Tennessee, 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 NCT00035516 about?

NCT00035516 is a clinical study titled "A Phase II Study of Epothilone Analog BMS-247550 in Patients With Non-Small Cell Lung Cancer Who Have Failed First Line Platinum Based Chemotherapy". The purpose of this clinical research study is to learn if BMS-247550 can shrink or slow the growth of the cancer in patients with non-small cell lung cancer who have failed first-line platinum based chemotherapy. The safety of this treatment will also be studied.

What is the current status of trial NCT00035516?

This trial is currently completed. It is a Phase 2 study. The study started on 2001-02. Estimated completion is 2004-04.

What conditions does trial NCT00035516 study?

This clinical trial studies the following conditions: Carcinoma, Non-small-cell Lung. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00035516?

The interventions under investigation include: Epothilone (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00035516?

This trial is sponsored by R-Pharm, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00035516 being conducted?

This trial has 16 study locations across Alabama, California, Florida, Illinois, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial