Eligibility Module

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: 2025-12-24 @ 5:06 PM
Ignite Modification Date: 2025-12-24 @ 5:06 PM
NCT ID: NCT00849550
Eligibility Criteria: Inclusion Criteria: * Must be 18 years or older * Must have a performance status of at least 70% (able to carry on most normal activities) * Must have life expectancy of at least 3 months * Must have adequate organ and marrow function as determined by lab tests * Women of child-bearing potential and men must agree to use two forms of contraception * Ability and willingness to sign a written informed consent document * Histologically confirmed solid tumor malignancy that is metastatic or unresectable Exclusion Criteria: * Pregnant or breastfeeding and/or lactating women * Patients who have received any other investigational agents within 28 days of the first day of study drug * Patients with known CNS metastases * History of other carcinomas within last 5 years (except non-melanoma skin cancer, in-situ cervical cancer, localized prostate cancer) * Inadequately controlled hypertension * Significant vascular disease * Invasion or encasement of a major artery * Evidence of bleeding diathesis or coagulopathy * Major surgical procedure, open biopsy or significant traumatic injury within 28 days prior to day 1 of study drug * Serious illness or medical condition * History of myocardial infarction, unstable angina, cardiac or other vascular stenting * History of stroke * HIV, Hepatitis C, Hepatitis B or other serious chronic infection * Impairment of Gastrointestinal function or disease * History of interstitial lung disease * Patients who have had radiation therapy, hormonal therapy, biologic therapy or chemotherapy for cancer within 28 days of receiving study drug.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT00849550
Study Brief:
Protocol Section: NCT00849550