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 @ 1:23 AM
Ignite Modification Date:
2025-12-25 @ 1:23 AM
NCT ID:
NCT01634893
Eligibility Criteria:
Inclusion Criteria:
* Able to provide informed consent
* Not on immune-modulating drugs, except those used as study drug premedication, unless the principal investigator grants an exception (which exception must be documented in writing)
* Patients with relapsed or refractory solid tumors with no viable treatment options
* Measurable disease within 30 days of study enrollment
* Blood hemoglobin \> 8.5 gm/dl within 7 days of study enrollment
* Absolute neutrophil count \> 1000/mm3 within 7 days of study enrollment
* Platelet count \> 50,000/mm3 within 7 days of study enrollment
* SGOT \<10x upper limit of normal within 7 days of study enrollment
* No chemotherapy or radiation therapy in the 14 days prior to initiation of treatment on this study. No other concurrent chemotherapy, surgery or radiation therapy during this protocol except surgery or radiation therapy to control symptoms with concurrence of the principal investigator.
* No contraindication to any study treatment
* No active major medical problems, including untreated or uncontrolled infections
* If of reproductive potential, a negative urine or blood pregnancy test within 3 days of study enrollment, and agreement to use adequate contraception. In relevant subjects, pregnancy testing will continue monthly while on treatment unless the subject is no longer able to become pregnant or there is sufficient justification otherwise
* Not breast feeding
* Life expectancy \> 6 months
* ECOG performance status \< 2
* Age 18+ years
* No active substance abuse in the prior 6 months
* Not on digoxin or cimetidine
Exclusion Criteria:
* Contraindication or hypersensitivity to any study drug or its components or excipients
* Current pregnancy or breast feeding
* Inability to document adequate contraception if a female of reproductive potential
* Chemotherapy or radiation therapy within the 14 days prior to initiation of study treatment
* Prior treatment with sorafenib. Prior HCQ use is not an exclusion.
* Life expectancy \< 6 months
* ECOG performance status \> 2
* Symptomatic coronary artery disease (including uncontrolled angina, congestive heart failure, and the like)
* Uncontrolled hypertension (diastolic BP consistently \>100 mm Hg or systolic BP consistently \>160 mm Hg on a regular basis)
* Uncontrolled, symptomatic cardiac arrhythmia
* Active substance abuse in the prior 6 months
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01634893
Study Brief:
Protocol Section:
NCT01634893