Clinical trial · Interventional
Ixabepilone in Treating Patients With Metastatic, Recurrent, or Unresectable Kidney Cancer
A Phase II Trial of BMS 247550 (Ixabepilone) in Advanced Renal Cell Carcinoma
NCT00182702CI-TRIAL-00009804completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This phase II trial is studying how well ixabepilone works in treating patients with metastatic, recurrent, or unresectable kidney cancer. Drugs used in chemotherapy, such as ixabepilone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Clear Cell Renal Cell Carcinoma | Clear Cell Renal Cell Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Recurrent Renal Cell Cancer | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
| Stage III Renal Cell Cancer | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
| Stage IV Renal Cell Cancer | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ixabepilone | Drug | — | UNRESOLVED |
| laboratory biomarker analysis | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment
- description
- Patients receive ixabepilone IV over 3 hours on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
- interventionNames
- Drug: ixabepilone
- Other: laboratory biomarker analysis
Primary outcomes (1)
- measure
- Objective response rate (partial or complete)
- timeFrame
- Up to 5 years
Secondary outcomes (2)
- measure
- Progression-free survival (PFS)
- timeFrame
- From the start of treatment to time of progression, assessed up to 5 years
- description
- PFS rate will be estimated using the Kaplan-Meier method. Median PFS time and its associated 90% confidence interval will be estimated using the method of Brookmeyer and Crowley.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically or cytologically confirmed renal cell carcinoma of 1 of the following subtypes: * Clear cell * Papillary, type I or II * Chromophobe * Collecting duct * Medullary * Metastatic, recurrent, or unresectable disease * Measurable disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm by spiral CT scan * No known active brain metastases requiring steroid or anticonvulsant therapy * Patients with definitively treated brain metastases are eligible provided they are not on steroids or anticonvulsants AND show no evidence of disease progression for ≥ 3 months after completion of definitive therapy * Performance status - ECOG 0-2 * At least 3 months * WBC ≥ 3,000/mm\^3 * Absolute neutrophil count ≥ 1,500/mm\^3 * Platelet count ≥ 100,000/mm\^3 * Bilirubin ≤ 1.5 times upper limit of normal (ULN) * AST and ALT ≤ 2.5 times ULN * Creatinine ≤ 1.5 times ULN * Glomerular filtration rate ≥ 50 mL/min * No symptomatic congestive heart failure * No unstable angina pectoris * No cardiac arrhythmia * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * No ongoing or active infection * No HIV positivity * No peripheral neuropathy \> grade 1 * No psychiatric illness or social situation that would preclude study compliance * No history of allergic reaction attributed to compounds of similar chemical or biological composition to study drug * No history of severe hypersensitivity reaction to agents containing Cremophor® EL * No other active malignancy * Curatively treated malignancies are allowed provided the risk of recurrent disease at the time of study enrollment is \< 20% * No other uncontrolled illness * More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered * No prior tubule inhibitors, including, but not limited to, any of the following: * Vinca alkaloids (e.g., vinblastine, vincristine, or vinorelbine) * Taxanes (e.g., docetaxel or paclitaxel) * Epothilones * No other concurrent chemotherapy * See Disease Characteristics * No concurrent hormonal therapy except steroids for adrenal failure or hypersensitivity prophylaxis or hormones for non-disease related conditions (e.g., insulin for diabetes) * More than 4 weeks since prior radiotherapy and recovered * No concurrent palliative radiotherapy * No other concurrent investigational agents * No other concurrent anticancer therapy
References
Publications (0)
Data not yet available
No reference posted for this study.