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 @ 5:03 AM
Ignite Modification Date:
2025-12-25 @ 5:03 AM
NCT ID:
NCT00493818
Eligibility Criteria:
Inclusion Criteria:
* Confirmed diagnosis of solid tumor malignancy or lymphoma that is not responsive to standard therapies or for which there is no approved therapy
* Female patients of child-bearing potential must be willing to abstain from intercourse from 2 weeks prior to administration of the first dose of study medication until 28 days after the final dose of study medication or be willing to consistently and correctly use an acceptable method of birth control.
Exclusion Criteria:
* Prior anti-cancer therapy within the prior 28 days.
* History of diabetes.
* Coronary artery disease/myocardial infarction, acute coronary syndromes within the past 6 months.
* Use of theophylline and warfarin within 14 days prior to the first dose of study drug.
* Current use of oral corticosteroids (note: Inhaled corticosteroids are permitted.)
* Participation in an investigational study within the prior 28 days.
* Pregnant or breast-feeding.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00493818
Study Brief:
Protocol Section:
NCT00493818