- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00090727
Chemotherapy for Patients With Advanced Solid Tumors or Non-Hodgkin's Lymphoma
A Phase 1, Open-Label, Dose-Escalation Study of AQ4N Administered Intravenously in Patients With Advanced Malignancies
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
Study Overview
Status
Conditions
Intervention / Treatment
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.
Study Type
Enrollment
Phase
- Phase 1
Contacts and Locations
Study Locations
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New York
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Bronx, New York, United States, 10461
- Weiler Hospital of Albert Einstein College of Medicine
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Texas
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San Antonio, Texas, United States, 78229
- Cancer Therapy & Research Center / Institute for Drug Development
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 021-001
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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