Status:
COMPLETED
Dose-Escalating Study Of SB-485232 Administered Intravenously Every 28 Days To Adults With Solid Tumors Or Lymphomas
Lead Sponsor:
GlaxoSmithKline
Conditions:
Solid Tumor Cancer
Lymphoma
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
SB-485232 will be administered as five daily intravenous (IV) infusions repeated every 28 days in adult subjects with advanced solid tumors or lymphomas. Subjects may receive up to 6 cycles of treatme...
Eligibility Criteria
Inclusion
- Inclusion criteria:
- Histopathological confirmation of cancer limited to a solid tumor malignancy or follicular lymphoma.
- Advanced or metastatic disease.
- Measurable disease.
- Females of child-bearing potential must use adequate birth control.
- Karnofsky Performance Status of 70% or greater.
- Predicted life expectancy of at least 12 weeks in the estimation of the physician conducting the study (Principal Investigator).
- Adequate laboratory results.
- Subjects with history of coronary artery disease must have a stress test without clinically significant abnormalities.
- Subjects with a history of congestive heart failure, myocardial infarction or prior anthracycline chemotherapy, must have a MUGA (Multiple Gated Acquisition) scan which demonstrates a left ventricular ejection fraction equal to or greater than 40%.
- Signed informed consent form
- Exclusion Criteria:
- Female subject is pregnant or nursing (lactating).
- Active, chronic or uncontrolled infections requiring systemic antibiotic therapy.
- Serious medical or psychiatric disorder that would interfere with the subject''s safety or ability to sign the informed consent.
- Leptomeningeal disease or evidence of prior or current metastatic brain disease.
- Receiving concurrent chemotherapy, immunotherapy, radiotherapy, corticosteroid therapy, or investigational therapy.
- Received chemotherapy, radiotherapy, immunotherapy, hormonal therapy or biological therapy for cancer or underwent a surgical procedure (except for minor surgical procedures) within 4 weeks before beginning treatment with SB-485232 (6 weeks in case of nitrosureas or mitomycin C).
- Exposed to an investigational drug within 30 days or 5 half-lives (whichever is longer) preceding the first dose of SB-485232.
- Severe concurrent disease or condition, including clinically significant autoimmune disease, which in the judgement of the physician conducting the study (the principal investigator) would render the patient inappropriate for study participation.
- History of ventricular arrhythmias requiring drug or device therapy.
- An unresolved or unstable, serious toxicity from prior administration of another investigational product.
- Psychological, familial, sociological, or geographical limitations that do not permit compliance with this protocol.
- Received prior SB-485232 therapy.
- Poor venous access.
Exclusion
Key Trial Info
Start Date :
April 1 2004
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT00085904
Start Date
April 1 2004
Last Update
October 13 2008
Active Locations (3)
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1
GSK Investigational Site
Indianapolis, Indiana, United States, 46202
2
GSK Investigational Site
Boston, Massachusetts, United States, 02215
3
GSK Investigational Site
Pittsburgh, Pennsylvania, United States, 15213-2584