Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:25 AM
Ignite Modification Date:
2025-12-25 @ 4:25 AM
NCT ID:
NCT00580320
Eligibility Criteria:
Inclusion Criteria:
* Histologic diagnosis of cutaneous or mucosal melanoma, soft tissue sarcoma (STS), or an APUD (amine precursor uptake and decarboxylation) tumor. APUD tumors include parathyroid carcinoma, medullary carcinoma of the thyroid, small cell carcinoma of the lung, pheochromocytoma, islet cell tumors, carcinoid tumors, and malignant paraganglioma.
* Measurable or evaluable disease not appropriate for resection and/or radiation with curative intent. Patients with small cell carcinoma must have extended stage disease or, if limited stage disease, must have received at least one prior systemic therapy.
* Age 18 years or greater
* ECOG Performance Status 0 or 1
* Women must be post-menopausal, infertile as the result of a surgical procedure, or willing to use a medically accepted form of birth control (abstinence, hormonal contraceptive, intra-uterine device, diaphragm with spermicide, condon with spermicide) for the duration of study treatment. Men also must agree to use a medically accepted form of birth control for the duration of study treatment.
Exclusion Criteria:
* Uncontrolled brain metastatic disease
* Platelet count \<100
* Absolute neutrophil count \<1.5
* Blood transfusion or hematopoietic growth factors for cytopenia within one month of enrollment.
* Calculated or measured (Cockcroft and Gault formula) creatinine clearance \<30 mL/minute
* AST \> 3 times the upper limit of normal, unless elevation due to metastatic disease, in which case AST \> 5 times the upper limit of normal
* Bilirubin \> 2 mg/mL
* Grade 2 or greater peripheral neuropathy
* Hypersensitivity to bortezomib, boron, mannitol, or dacarbazine
* Pregnant or nursing
* Other investigational drugs within 14 days of enrollment
* Other medical or other condition(s) that in the opinion of the investigator/sub-investigator might compromise the objectives of the study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00580320
Study Brief:
Protocol Section:
NCT00580320