Able to give written informed consent and comply with all study visits and procedures.
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Willingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigator
Able to understand and comply with the study procedures, understand the risks involved in the study, and provide written informed consent before the first study-specific procedure; specifically able to comply with the PK assessment schedule during the first  treatment cycles.
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Subject has any medical, psychiatric, addictive or other disorder which compromises the ability of the subject to give written informed consent and/or to comply with procedures
Willingness and ability to provide written informed consent prior to any study?related procedures and to comply with all study requirements.
Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements
Willing and able to provide written Informed Consent and comply with the requirements of the study.
Male or female ?  years of age. . Weigh ?  kg. . ECOG performance score -, inclusively. . Negative ?-hCG test in women of childbearing potential. . Able to understand and comply with the requirements of the study and to provide written informed consent.
Subject should be able to provide written informed consent, comply with protocol visits and procedures, be able to take oral medication, and not have any active infection or comorbidity that would interfere with therapy.
Male or female, ?  years old with the ability to understand and provide signed and witnessed informed consent, and agree to comply with protocol requirements
Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements
Able to understand and comply with the requirements of the study and to provide written informed consent or age appropriate assent for pediatric patients.
Able to understand and give written informed consent and comply with study procedures.
Willingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigator
Any medical, psychiatric, addictive or other kind of disorder which compromises the ability of the subject to give written informed consent and/or to comply with procedures
Able to provide written, informed consent before initiation of any study related procedures, and is able, in the opinion of the Investigator, to comply with all the requirements of the study.
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements
Any medical, psychiatric, addictive or other kind of disorder which compromises the ability of the subject to give written informed consent and/or to comply with procedures
Patient has any kind of disorder that compromises the ability of the patient to give written informed consent and/or to comply with study procedures
Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Ability to provide signed informed consent and willing and able to comply with all study requirements
Has any medical or psychiatric disorder that compromises the ability of the subject to give written informed consent, and/or comply with the study procedures.
Be willing and able to understand and give written informed consent and comply with all study related procedures
Able to give written informed consent and comply with all study visits and procedures
Willingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigator
Subject must be able to provide written informed consent, comply with protocol visits and procedures, and take oral medication, and does not have any active infection or comorbidity that would interfere with therapy
Patient understands the nature of the procedure, is willing to comply with associated followup evaluations, and provide written informed consent prior to the procedure
Subject is able to provide written informed consent, comply with protocol visits and procedures, and take oral medication, and does not have any active infection or comorbidity that would interfere with therapy.
Able and willing to provide written informed consent and to comply with the study protocol
Willing and able to comply with the study procedures and provide written informed consent to participate in the study
Be able and willing to provide written informed consent and to comply with all requirements of study participation (including all study procedures);
Ability to provide written informed consent and to understand and comply with the requirements of the study
Has provided written informed consent, and has the willingness and ability to comply with all study procedures
Willingness and ability to provide written informed consent and to comply with the study protocol as judged by the investigator
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol.
Must provide informed consent and HIPPA authorization and agree to comply with all protocol-specified procedures and follow-up evaluations
Able and willing to provide written informed consent and to comply with the study protocol
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements
Ability and willingness to provide written informed consent, and to comply with the requirements of the protocol
Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements.
Ability to provide written informed consent and comply with study requirements
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements
Patients must provide signed, written, informed consent and be willing and able to comply with eligibility requirements, scheduled, visits, and follow-up studies
Any medical, psychiatric, addictive or other disorder which compromises the ability of the subject to give written informed consent and/or to comply with procedures.
Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements.
able understand and give written informed consent and comply with the study protocol.
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements
Subject has any kind of disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures.
Willingness and ability to provide written informed consent prior to any study-related procedures and comply with all study requirements.
Any condition that may compromise the ability to give written informed consent or to comply with the study protocol.
Able to understand and give written informed consent and comply with study procedures.
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements.
Able to understand and give written informed consent and comply with study procedures.
Ability to give written informed consent and willing to comply with the requirements of the protocol; and for Part , to give written informed consent for  cancer biopsy procedures
Willingness and ability to provide written informed consent and to comply with the protocol requirements
Ability to provide written informed consent, comply with protocol visits and procedures, take oral medication, and not have any active infection or chronic comorbidity that would interfere with therapy
Subject should be able to provide written informed consent and comply with protocol visits and procedures.
Must be willing and able to provide written informed consent and comply with the protocol and study procedures
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements and for  months after last dose.
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol.
Have the ability to understand the requirements of the study, provide written informed consent (including consent for the use and disclosure of research-related health information), and comply with the study and follow-up procedures.
Provide written informed consent and willing to comply with protocol requirements.
Subject has any kind of disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
the ability to comply with the study protocol and provide informed consent
Able to provide written informed consent and willing to comply with protocol requirements
Subjects able to provide informed consent and agree to comply with study procedures
Signed written informed consent and willingness to comply with protocol requirements
Able to understand and comply with study procedures, understand the risks involved, and provide written informed consent.
Able to provide written informed consent, comply with protocol visits and procedures, be able to take oral medication, and not have any active infection or comorbidity that would interfere with therapy.
Ability to give informed consent and to comply with study procedures
Able to provide written informed consent and willing to comply with protocol requirements
Provides written informed consent and willing to comply with protocol requirements
Provide written informed consent and willing to comply with protocol requirement