CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 102 enrolled
Drug / intervention
BMS-247550 +2 moredrug
Likely dose
BMS-247550 6 mg/m² daily for 5 consecutive days every 3 weeks (30 mg/m² per cycle)AI-extracted
Key inclusion· 10
  • Age ≥18 years
  • Histologically or cytologically confirmed renal cell carcinoma (clear cell, papillary type I/II, chromophobe, collecting duct, or medullary)
  • Prior IL-2 experience, or evaluated/deemed ineligible for IL-2, or refused IL-2
  • Measurable disease
Key exclusion· 7
  • CNS metastases unless controlled with radiation or surgery ≥6 months prior to enrollment
  • Poor medical risk due to non-malignant systemic disease or active, uncontrolled infection
  • HIV seropositive status
  • Prior craniospinal radiation or total body irradiation

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00030992
NCT00030992Phase 2Completed

A Phase II Clinical Trial of BMS-247550 (NSC 710428), an Epothilone B Analog, in Renal Cell Carcinoma

National Cancer Institute (NCI)·interventional·Posted Feb 21, 2002·Updated Aug 20, 2012

In Brief

A Phase 2 clinical trial evaluating BMS-247550, Ranitidine, and 1 other intervention for Renal Cell Carcinoma. Completed, enrolled 102 participants across 1 site.

Detailed Summary

This study will examine whether the experimental drug BMS 247550 (Ixabepilone) is an effective treatment for kidney cancer. BMS 247550 belongs to a class of drugs called epothilones that interfere with the ability of cancer cells to divide. In the way they kill cells, they are very similar to a class of compounds known as the taxanes, which include the drug Taxol. Other characteristics of the epothilones, however, enable them to work in cells that are resistant to Taxol. Patients 18 years of age or older with kidney cancer that has not spread to the central nervous system (unless the brain tumor has remained stable for at least six months after surgical or radiation treatment) may be eligible for this study. Pregnant or nursing women may not participate. Candidates are screened with various tests that may include blood and urine tests, electrocardiogram (EKG), and chest x-ray. Computerized tomography (CT) scans or X-rays, and possibly nuclear medicine studies may be done to determine the extent of disease. Participants receive BMS 247550 by a 1-hour infusion into a vein for 5 consecutive days (days 1, 2, 3, 4 and 5) of each 21-day treatment cycle. Patients must stay in the National Institutes of Health (NIH) area near Bethesda, Maryland, for 7 to 8 days during the first treatment cycle and for the 5 days of treatment in subsequent cycles. The total number of cycles will vary among patients, depending on their individual clinical situation. The drug dose may be increased gradually in subsequent cycles in patients who can tolerate such increases. In addition, participants undergo the following tests and procedures: * Periodic physical examinations and frequent blood tests * X-ray and other imaging studies to determine if the tumor is responding to the treatment. * Tumor biopsies to confirm the diagnosis or spread of tumor and to examine the reaction of certain proteins in cancer cells to BMS 247550. Two biopsies will be done. For this procedure, a small piece of tumor tissue is withdrawn through a needle under local anesthetic. Treatment will be stopped in patients whose tumor grows while receiving BMS 247550. Patients whose tumor disappears completely will be followed at NIH periodically for examinations and tests. Patients whose disease does not completely resolve or whose disease recurs may be advised of other appropriate research protocols at NIH or, if none are available, will be returned to the care of their local doctor.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 21, 2002
Enrollment StartFeb 1, 2002
Primary CompletionJan 1, 2009
Study CompletionJun 1, 2012
TodayJul 2, 2026
Enrollment to primary: 6.9 yearsPosted 24.4 years ago

Interventions

BMS-247550drug

One hour infusion on five successive days (daily x 5) every three weeks. Starting dose of 6 mg/m\^2/day for a total per cycle dose of 30 mg/m\^2

Ranitidinedrug

50 mg 30-60 minutes prior to Ixabepilone (BMS-247550)

Diphenhydraminedrug

50 mg intravenously 30-60 minutes prior to Ixabepilone (BMS-247550)