Signed informed consent prior to study specific procedures.
Signed informed consent prior to the performance of any study-specific procedures, including fresh tumor biopsies.
Signed informed consent/authorization is obtained prior to conducting any study-specific screening procedures.
Signed written informed consent granted prior to initiation of any study-specific procedures.
Provide signed, written informed consent prior to the initiation of any study-specific procedures
The patient has signed informed consent prior to initiation of any study-specific procedures or treatment.
Patient must give study-specific informed consent on an IRB-approved consent prior to any research-related procedures or study treatment.
The patient has not signed a study-specific informed consent for this study.
Signed, informed consent must be obtained prior to any study specific procedures
Have signed an informed document prior to any study-specific procedures or treatment
Signed study-specific informed consent
Signed informed consent obtained prior to initiation of any study-specific procedures and treatment;
Signed, informed consent must be obtained prior to any study specific procedures
Ability to understand and the willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
Written informed consent/assent prior to any study-specific procedures
Signed written informed consent granted prior to initiation of any study-specific procedures
Signed informed consent prior to the start of any study specific procedures.
Subject understood and signed the study specific informed consent
Ability to understand and willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
Signed informed consent prior to the start of any study specific procedures.
Signed informed consent prior to initiation of any study-specific procedure or treatment
Signed study-specific informed consent prior to study entry
Signed study-specific informed consent form prior to study entry
Signed study-specific informed consent prior to study entry
Signed informed consent before initiation of any study procedures.
Ability to sign informed consent form; informed consent form for this study must be signed prior to the performance of any study-specific procedures and initiation of any study therapy
The patient has signed informed consent prior to initiation of any study-specific procedures or treatment.
The patient has signed informed consent prior to initiation of any study-specific procedures or treatment.
Signed study-specific informed consent
Signed written informed consent before performance of study-specific procedures or assessments and must be willing to comply with treatment and follow up
Signed informed consent obtained prior to initiation of any study-specific procedures and treatment as confirmation of the patient’s awareness and willingness to comply with the study requirements (inclusive of 2 biopsies, one at baseline and if they qualify, one pre-randomization for part 2B)
Signed informed consent prior to any protocol-specific procedures
Ability to understand and the willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
The patient has signed informed consent prior to initiation of any study-specific procedures or treatment.
Provided informed consent prior to initiation of any study-specific activities/procedures
Ability to understand and the willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
Signed, informed consent must be obtained prior to any study specific procedures
Signed, informed consent must be obtained prior to any study specific procedures.
Signed informed consent prior to the start of any study specific procedures.
Signed a protocol-specific informed consent
Signed, informed consent must be obtained prior to any study specific procedures.
Signed study-specific informed consent
Have given written informed consent prior to any study-specific procedures
Have given written informed consent prior to any study-specific procedures
Signed study-specific informed consent
Signed written informed consent granted prior to initiation of any study-specific procedures
Have signed an informed document prior to any study-specific procedures or treatment
Ability to understand and the willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
Signed study-specific informed consent prior to registration
Ability to understand and willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
Ability to understand and the willingness to sign a written informed consent. A signed informed consent must be obtained prior to any study specific procedures.
Written informed consent before any study-specific procedure is performed
Informed consent given prior to study-specific screening procedures
Have signed written informed consent prior to the initiation of any study-specific procedures
A signed informed consent must be obtained prior to any study-specific procedures.
Written informed consent prior to completing any study-specific procedure
Signed written informed consent from either the subject, or their legally acceptable representative if the subject is incapable of giving their own consent, prior to performing any study-specific tests or procedures.
Give written informed consent prior to any study-specific procedures.
Willing and able to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
Ability to understand and to sign an informed consent form; a signed informed consent must be obtained prior to any study specific procedures
Before any study-specific procedure is performed, the appropriate written informed consent must be obtained
Must give study specific informed consent prior to enrollment. For re-administration, patients must be re-consented.
Ability to understand and the willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures
Written informed consent before any study-specific procedure is performed
Subjects must give written informed consent to participate in study. Consent must be obtained prior to the performance of any study-specific, non-institutional standard procedures. A copy of the signed informed consent will be retained in the subject's chart.
Signed a study-specific informed consent prior to study entry
Signed study-specific informed consent prior to registration
Signed, specific informed consent prior to study entry
Signed, specific informed consent prior to study entry
Valid written informed consent signed by the patient prior to any study-specific procedures
Ability to understand and the willingness to sign a written informed consent. A signed informed consent, including consent for biomarker analyses, must be obtained prior to any study-specific procedures
Signed informed consent prior to any protocol-specific procedures