CPT-11 and 5Fluorouracil (5FU) combined with leucovorin has become the standard of care for colorectal cancer. PN401 permits treatment with higher than normal doses of 5FU, which could increase its therapeutic potential. It is hypothesized that adding PN401 to the CPT-11, 5FU, leucovorin regimen will reduce toxicity and will allow higher doses of 5FU to be well tolerated and therefore potentially increase effectiveness.

Condition	Treatment or Intervention	Phase
Solid Tumors	Drug: triacetyluridine  Drug: fluorouracil  Drug: leucovorin  Drug: camptosar	Phase I

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria

• Must be at least 18 years of age;
• Life expectancy: At least 3 months;
• Performance status: ECOG of 0 or 1;
• Histologic or cytologic proof of a solid tumor cancer that is not amenable to curative surgical resection;
• Evaluable or measurable disease documented within 4 weeks of the start of treatment;
• Prior chemotherapy or radiotherapy is allowed if 4 weeks or more have elapsed prior to starting treatment and patients have recovered from toxicities of prior treatment;
• Adequate organ function: Hematopoietic: ANC = 1500/ul or more, Platelets = 100,000/ul or more, Hemoglobin = 9.5 g/dL or more, transfusion prior to evaluation is allowed; Hepatic: Bilirubin = 2.0 mg/dL or less and SGPT(ALT) and SGOT(AST) < 3 x upper limit of normal (< 5 x upper limit of normal if liver metastases present) Renal: Serum Creatinine < 2.0 mg/dL;
• Patient has the initiative, geographic proximity, and means to be compliant with the protocol;
• Fertile patients (male or female) must agree to use effective contraception;
• Must be able to swallow and retain tablets.

Exclusion Criteria

• Major surgery within the four weeks preceding the start of treatment;
• Serious medical or psychiatric illness that would prevent self-determined informed consent;
• Intensive chemotherapy treatment;
• Infection or antibiotics at the time of screening;
• Uncontrolled cardiovascular, pulmonary, renal, neurologic, psychiatric, or hepatic dysfunction;
• Pregnant or nursing;
• Pre-existing diarrhea or uncontrolled clinically significant illness other than cancer (i.e. ulcerative colitis, malabsorption syndrome);
• Brain metastases that have not been stable for more than 3 months;
• Known Dihydropyrimidine Dehydrogenase (DPD) deficiency.

Maryland
      University of Maryland, Greenebaum Cancer Center, Baltimore,  Maryland,  21201,  United States; Recruiting

Study ID Numbers:  401.02.001; GCC0121
Record last reviewed:  September 2002
Record first received:  September 4, 2002
ClinicalTrials.gov Identifier:  NCT00044785
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2004-11-10