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 @ 11:31 PM
Ignite Modification Date:
2025-12-24 @ 11:31 PM
NCT ID:
NCT01553656
Eligibility Criteria:
Select Inclusion Criteria:
* Subjects with advanced or metastatic solid tumors for whom the standard of care is ineffective or inappropriate.
* NSCLC expansion cohort subjects must have confirmed NSCLC (Stage IIIb or IV) and documented activating mutations.
* At least 4 weeks must have elapsed from the last anti-cancer therapy. At least 6 weeks for nitrosoureas, mitomycin C and liposomal doxorubicin.
* Have adequate bone marrow function, adequate liver function, and adequate renal function.
* Sexually active subjects (men and women of child-bearing potential (WOCBP)) must agree to use medically accepted barrier methods of contraception (eg, male or female condom) during the course of the study and for 4 months after the last dose of study drug(s), even if oral contraceptives are also used. All subjects of reproductive potential must agree to use both a barrier method and a second method of birth control. Women of childbearing potential (WOCBP) must have a negative pregnancy test at screening.
Select Exclusion Criteria:
* Symptomatic central nervous system (CNS) metastasis, or active CNS metastasis requiring medication.
* WOCBP who are unwilling or unable to use an acceptable method of contraception to avoid pregnancy for the entire study period and for 4 months after the last dose of investigational product.
* Women who are pregnant or breastfeeding.
* Sexually active fertile men not using effective birth control for the entire study period and for 4 months after the last dose of investigational product if their partners are WOCBP.
* Subjects who have uncontrolled intercurrent illness including, but not limited to, infection requiring systemic therapy, symptomatic congestive heart failure, uncontrolled hypertension, uncontrolled angina pectoris, uncontrolled peptic ulcer, cardiac arrhythmia requiring medication.
* Subjects who are HIV antibody positive, HBs antigen positive, and/or HCV antibody positive.
* Subjects with body cavity fluid retention which requires drainage.
* Subjects with any major surgery within 8 weeks prior to study enrollment.
* Subjects with major unhealed wounds or fracture.
* Subjects with a history or concurrent diagnosis of gastrointestinal perforation.
* Subjects with evidence of bleeding tendency or coagulopathy.
* Subjects with a history of thromboembolism.
* Subjects with a history of or concurrent pancreatitis.
* Exposure to any investigational drug within 30 days of enrollment.
* Subjects receiving radiation therapy or treatment with radionuclides within 6 to 2 weeks before first dose of XL184.
* NSCLC expansion cohorts: subjects must not be diagnosed with another malignancy within 2 years before first dose of XL184.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Study:
NCT01553656
Study Brief:
Protocol Section:
NCT01553656