Able to give written informed consent and comply with all study visits and 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.
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.
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 comply with the study procedure and sign a written informed consent
Able to understand and give written informed consent and comply with study procedures.
Be willing and able to provide written informed consent for the trial and comply with the study visit requirements
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
After being fully informed about their illness and the investigative nature of the protocol (including foreseeable risks and possible toxicities), is willing and able comply with the protocol and to provide written, ethics committee-approved informed consent form before performance of any study-specific procedures or examinations
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
Understand the study requirements and the treatment procedures, and is willing to comply with all specified follow-up evaluations, and provides written informed consent before any study-specific tests or procedures are performed.
Ability to provide signed informed consent and willing and able to comply with all study requirements
Able to provide informed consent and comply with all study protocols
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 and willing to provide informed consent and to comply with the study procedures
Able to give written informed consent and comply with all study visits and procedures
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
Able and willing to provide written informed consent prior to performing any study-related procedures and to comply with the study protocol, including patients must be willing and able to use the electronic patient-reported outcome (ePRO) device
Must be willing and able to participate and comply with all trial requirements and able to provide signed and dated informed consent prior to initiation of any trial procedures
Patient understands the procedures and agrees to comply with the study requirements by providing written informed consent
Patient understands the nature of the procedure, is willing to comply with associated follow–up 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
Adult subjects ?18 years of age who are able to understand study procedures, comply with them, and provide written informed consent before any study-specific procedure.
Be able and willing to provide written informed consent and to comply with all requirements of study participation (including all study procedures);
Has provided written informed consent, and has the willingness and ability to comply with all study procedures
Adult subjects ?18 years of age who are able to understand and comply with study procedures, and provide written informed consent before any study-specific procedure.
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
Be willing and able to provide written informed consent for the trial and comply with the study visit requirements
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements
Ability to understand the purpose of the study, provide signed and dated informed consent, and able to comply with all procedures
Ability to understand the nature of this study protocol, comply with study and/or follow-up procedures, and give written informed consent
Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements.
Patients must be willing and able to comply with the protocol and provide written informed consent prior to study specific screening procedures
Patient understands the procedures and agrees to comply with the study requirements by providing written informed consent
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
Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.
Subjects willing and able to comply with all aspects of the protocol for the duration of the study and provide written informed consent before any study-specific screening procedures are performed, with the understanding that the subject may withdraw consent at any time without prejudice
Willing and able to provide written informed consent prior to any study related procedures and to comply with all study requirements.
Be willing and able to give written informed consent, and be able to comply with all study procedures
Subjects willing and able to comply with the study protocol for the duration of the study and provide written informed consent prior to any study-specific screening procedures with the understanding that the subject may withdraw consent at any time without prejudice.
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.
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 3, to give written informed consent for 2 cancer biopsy procedures
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.
The subject has read and understood the written informed consent form (ICF) and is willing and able to give informed consent, fully understands the requirements of the trial and is willing to comply with all trial visits and assessments, including completion of patient-reported measures. Consent must be given before any trial related activities.
Must be willing and able to provide written informed consent and comply with the protocol and study procedures
Be willing and able to give written informed consent, and be able to comply with all 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 3 months after last dose.
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
Able to give informed consent, and comply with study procedures
Subject capable of providing written informed consent prior to initiation of any study procedures; subjects able to understand and comply with planned study procedures and be available for all study visits
Able to provide written informed consent and willing to comply with protocol requirements
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
Subjects able to provide informed consent and agree to comply with study procedures
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
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
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