Clinical trial · Interventional
BMS-188797 and Carboplatin in Treating Patients With Advanced Nonhematologic Cancer
Phase I Study of BMS-188797 in Combination With Carboplatin in Patients With Advanced Malignancies
NCT00006086CI-TRIAL-00003894completedPhase 1ClinicalTrials.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)
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of BMS-188797 and carboplatin in treating patients who have advanced nonhematologic cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Unspecified Adult Solid Tumor, Protocol Specific | Adult Solid Neoplasm | ALIAS | 0.85 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| BMS-188797 | Drug | — | UNRESOLVED |
| carboplatin | Drug | Carboplatin | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed advanced nonhematologic malignancy that has progressed on standard therapy or for which no curative therapy exists * No brain metastases PATIENT CHARACTERISTICS: Age: * 18 and over Performance status: * ECOG 0-2 Life expectancy: * At least 3 months Hematopoietic: * Absolute neutrophil count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic: * Bilirubin no greater than 1.5 mg/dL * ALT and AST no greater than 2.5 times upper limit of normal (ULN) unless due to hepatic metastases Renal: * Creatinine no greater than 1.5 times ULN Other: * No chronic medical condition requiring treatment with corticosteroids * No prior severe hypersensitivity reaction to agents containing Cremophor (polyoxyethylated castor oil) * No serious uncontrolled medical disorder, active infection, or psychiatric disorder (e.g., dementia) that would preclude study * No preexisting neurotoxicity grade 1 or greater * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: * At least 4 weeks since prior immunotherapy and recovered * No concurrent immunotherapy Chemotherapy: * At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered * No more than 2 prior chemotherapy regimens for metastatic disease * No prior platinum or taxane therapy * No other concurrent chemotherapy Endocrine therapy: * At least 2 weeks since prior hormonal therapy (except megestrol for anorexia/cachexia) and recovered * At least 7 days since prior corticosteroids * No concurrent corticosteroids * No concurrent hormonal therapy Radiotherapy: * At least 4 weeks since prior radiotherapy to 30% or more of bone marrow and recovered * No concurrent radiotherapy Surgery: * Not specified Other: * No other concurrent investigational drug
References
Publications (1)
- RESULTFishman MN, Garrett CR, Simon GR, Chiappori AA, Lush RM, Dinwoodie WR, Mahany JJ, Dellaportas AM, Cantor A, Gollerki A, Cohen MB, Sullivan DM. Phase I study of the taxane BMS-188797 in combination with carboplatin administered every 3 weeks in patients with solid malignancies. Clin Cancer Res. 2006 Jan 15;12(2):523-8. doi: 10.1158/1078-0432.CCR-05-0928. PMID 16428495