Treating Patients With Advanced Solid Tumors, Breast Cancer or Recurrent Ovarian Cancer (NCT00005807) | Clinical Trial Compass
CompletedPhase 1
Treating Patients With Advanced Solid Tumors, Breast Cancer or Recurrent Ovarian Cancer
United States40 participantsStarted 2000-07
Plain-language summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.
PURPOSE: Phase I trial to study the effectiveness of BMS-247550 in treating patients who have metastatic, recurrent, or locally advanced, ovarian cancer, breast cancer, or metastatic or unresectable solid tumors.
Who can participate
Age range18 Years – 120 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Histologically or cytologically confirmed metastatic or unresectable solid malignancy for which no standard or curative therapies exist or are no longer effective
* Metastatic, recurrent, or locally advanced breast, ovarian, or other cancer
* Hemoglobin at least 9.0 g/dL
* WBC at least 3,000/mm3
* Absolute neutrophil count at least 1,500/mm3
* Platelet count at least 100,000/mm3
* Bilirubin normal
* AST/ALT no greater than 3 times upper limit of normal
* Gilbert's syndrome allowed
* Creatinine no greater than 2 mg/dL
Exclusion Criteria:
* symptomatic congestive heart failure
* unstable angina pectoris
* cardiac arrhythmia
* grade 2 or greater clinical neuropathy
* prior allergy or hypersensitivity reaction (grade 2 or greater) to prior paclitaxel or other therapy containing Cremophor EL
* allergy or intolerance to steroids, diphenhydramine, cimetidine, or ranitidine
* uncontrolled concurrent illness
* active infection
* pregnant or nursing
* other concurrent anticancer therapies or commercial agents
* other concurrent investigational agents
* other concurrent highly active antiretroviral therapy for HIV-positive patients