Non-Hodgkin's Lymphoma, Solid Malignancies
Conditions
Keywords
diffuse, follicular, chronic lymphocytic leukemia, colorectal cancer, pancreatic cancer, acute myelogenous leukemia, head and neck cancer, breast cancer, prostate cancer, ovarian cancer, bladder cancer, hypoxia, refractory, metastatic
Brief summary
The purposes of this study are to determine: * the largest dose of AQ4N that can be safely given once a week for three weeks out of a 4 week cycle * the side effects of AQ4N when given on the above schedule * how much AQ4N is in the blood and urine at specific times after administration and how the body get rids of AQ4N * if AQ4N helps treat cancer
Detailed description
This study is for people who have advanced cancer for which standard chemotherapy did not work or for which there are no reliably, effective treatments. AQ4N is an experimental chemotherapy that is thought to target tumor areas with low oxygen content and low blood supply; tumor areas that are usually the most resistant to standard chemotherapy and radiation treatment. AQ4N may be beneficial in cancer treatment by interfering with a protein that is required for cells to grow and divide, causing tumors to die or to delay their growth. All patients in this study will receive AQ4N. The dose will be increased for each new patient or group of patients until the maximum tolerated dose is reached.
Interventions
DRUGAQ4N
Sponsors
Novacea
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Advanced solid malignancy or non-Hodgkin's lymphoma that is refractory to treatment or has recurred * Age \> 18 years * Adequate hematologic (blood), kidney and liver function * Negative pregnancy test (females of childbearing potential only) * Willingness to use effective contraception by both males and females throughout the treatment period and for at least 2 months following treatment.
Exclusion criteria
* Any chemotherapy or radiation within the past 4 weeks * Symptomatic or uncontrolled brain metastases (patients with history of brain metastases who have had repeat brain scans within the past 30 days that demonstrate no evidence of tumor progression or brain swelling and who do not require corticosteriod treatment may be eligible) * Significant cardiovascular illness including, but not limited to, the following: active infection, uncontrolled hypertension, symptomatic congestive heart failure, unstable angina pectoris, heart attack within the past six months, or uncontrolled, irregular heart beat * Inadequate cardiac function * Prior investigational therapy within the past 28 days * Pregnant or breast feeding women
Countries
United States
Outcome results
None listed