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 @ 3:17 AM
Ignite Modification Date:
2025-12-25 @ 3:17 AM
NCT ID:
NCT00470405
Eligibility Criteria:
Inclusion Criteria:
* Pathologic or cytologic diagnosis of solid tumors or lymphoma
* Metastatic disease
* No curative or effective therapy exists
* Measurable or nonmeasurable disease
* No clinically relevant third-space fluid collections
* Fluid collections must be drained before study enrollment
* No leukemia
* No CNS metastases
Exclusion Criteria:
* ECOG performance status 0-2
* Life expectancy ≥ 12 weeks
* ANC ≥ 1,500/mm\^3
* Platelet count ≥ 100,000/mm\^3
* Hemoglobin ≥ 9 g/dL
* Bilirubin ≤ 1.5 times upper limit of normal (ULN)
* AST and ALT ≤ 3.0 times ULN (5 times ULN if liver has tumor involvement)
* Creatinine clearance ≥ 45 mL/min
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective contraception during and for 3 months after completion of study therapy
* No active infection or other serious illness that would preclude study participation
* No weight loss ≥ 10% within the past 6 weeks
* No peripheral neuropathy (e.g., diabetic neuropathy) ≥ CTC grade 1
* Must be able to take concurrent vitamin B12 and folic acid
PRIOR CONCURRENT THERAPY:
* No more than 1 prior chemotherapy regimen for metastatic disease
* More than 12 months since prior adjuvant therapy
* More than 30 days since prior drug that has not received regulatory approval
* More than 30 days since prior radiation therapy and recovered (alopecia allowed)
* Prior standard postoperative adjuvant radiation therapy for rectal cancer allowed
* No prior radiation therapy to ≥ 25% of bone marrow
* No prior oxaliplatin or pemetrexed disodium
* No NSAIDs or acetylsalicylic acid 2 days before (5 days for long-acting agents \[e.g., piroxicam\]), during, and for 2 days after each dose of pemetrexed disodium
* No concurrent nonpalliative radiation therapy or surgery for cancer
* No concurrent hormonal cancer therapy (except medroxyprogesterone)
* No other concurrent experimental medications (except thymidine)
* No other concurrent chemotherapy or immunotherapy
* No other concurrent anticancer therapy
* Concurrent palliative radiation therapy allowed for small areas of painful metastasis that cannot be managed adequately by systemic or local analgesics
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00470405
Study Brief:
Protocol Section:
NCT00470405