Signed, dated informed consent
Provision of signed and dated, written informed consent prior to any study specific procedures
Signed and dated informed consent
Written and voluntary informed consent understood, signed and dated.
Signed and dated written informed consent obtained prior to any study-specific evaluation.
Dated and signed IEC/IRB-approved informed consent.
Signed and dated written informed consent
Provision of signed and dated written informed consent prior to any study-specific procedures, sampling, and analyses. If a patient declines to participate in any voluntary exploratory research and/or genetic component of the study, there will be no penalty or loss of benefit to the patient and he/she will not be excluded from other aspects of the study.
Able to provide signed and dated informed consent before initiation of any study procedures.
Subject has signed and dated informed consent
Written and voluntary informed consent understood, signed and dated.
Patient must consent to the study and provide a signed and dated, written informed consent document prior to any study-specific procedures, sampling, or analyses.
Voluntarily signed and dated written informed consent prior to any specific-study procedure.
Patient has signed and dated informed consent
Signed and dated written informed consent.
Signed and dated written informed consent.
Signed and dated written informed consent obtained from patient or legal representative.
Signed and dated informed consent
Provision of signed and dated informed consent form (ICF).
Ability to provide a signed and dated consent or have a legally authorized representative to provide written and signed consent prior to the initiation of any research related procedures
Signed and dated written informed consent
Subject has signed and dated informed consent
Provision of signed and dated, written informed consent prior to any study specific procedures, sampling and analyses; including access to all archival tumour tissue (diagnostic and/or most recent samples)
Signed and dated PICF obtained prior to initiation of any study-specific procedure and treatment.
Signed and dated written informed consent
Provision of signed and dated, written Informed Consent Form (ICF) prior to any trial-specific procedures, sampling, or analyses. If a patient declines to participate in the voluntary pharmacogenetics component of the trial, he/she will not be excluded from other aspects of the trial.
Provide signed and dated informed consent prior to any study specific procedures.
Signed and dated written informed consent prior to admission to the study
Patients must have given written, signed and dated informed consent prior to registration on the study; NOTE: no study-specific screening procedures may be performed until consent has been given
A signed and dated written informed consent form is obtained from the subject
Signed and dated written informed consent
Signed and dated written informed consent
Signed and dated written ICF by the patient or legally acceptable representative prior to any study-specific procedures
Signed and dated informed consent of the patient, available before the start of any specific trial procedure.
Signed and dated informed consent document.
Informed consent document signed and dated by patient
Signed & dated informed consent prior to Screening evaluations
Must sign informed consent, witnessed, and dated prior to entry
Signed and dated written informed consent to participate in this clinical trial must be obtained prior to any study procedure
Provision of signed and dated, written informed consent prior to any study-specific procedures, sampling and analyses.
Signed and dated informed consent.
Patient provides signed and dated informed consent prior to initiation of any study procedures.
Provision of signed and dated, written informed consent
Provision of signed and dated written informed consent prior to any study specific procedures.
Signed and dated informed consent.
Provision of signed, written and dated informed consent prior to any study specific procedures
Provision of signed and dated, written informed consent prior to any study specific procedures, sampling and analyses
Provision of signed, written and dated informed consent prior to any study specific procedures
Signed and dated IRB/Approved Informed Consent
Able to provide signed and dated informed consent prior to initiation of any study procedures.
Signed and dated written informed consent prior to admission to the study
Subject has signed and dated informed consent
Signed & dated ICF prior to Screening evaluations
Patient must provide a signed and dated written informed consent prior to registration and any study-related procedures
PRE-REGISTRATION INCLUSION CRITERIA: Signed and dated informed consent document for study participation
Voluntarily signed and dated written informed consent
Voluntarily signed and dated written informed consent
Evidence of a personally signed and dated written informed consent to participate in the clinical study
Voluntarily signed and dated written informed consent
Signed and dated written informed consent
Written informed consent (IC) for trial participation must be signed and dated by the patient and the investigator prior to enrollment
Written consent to biological material submission, indicating the patient has been informed of and agrees to tissue and blood material use, transfer and handling, must be signed and dated by the patient and the investigator prior to any procedures specific for this trial
Signed and dated Informed Consent Form (by the patient or a legally acceptable representative as per the local regulations).
Signed and dated informed consent form (by the patient or a legally acceptable representative as per the local regulations) obtained prior to initiation of any study-specific procedure and treatment.
Provide signed and dated informed consent form
Written informed consent form signed and dated by the subject
Subject is capable of understanding and willing to provide a signed and dated written voluntary informed consent before any protocol specific procedures are performed
Signed and dated informed consent
Participant is able and willing to comply with study procedures, and signed and dated informed consent is obtained
Signed and dated written IRB approved informed consent;
Documented, signed, dated informed consent obtained prior to any study specific procedures being performed
Provide signed and dated informed consent form
Provide signed and dated informed consent form.
Patient, or the patient’s legally acceptable representative, must provide a signed and dated written informed consent prior to registration and any study-related procedures
Provision of signed and dated written informed consent prior to any study specific procedures, sampling analysis
Voluntarily signed and dated written informed consent prior to any specific study procedure.
Voluntarily signed and dated informed consent
Signed and dated informed consent document obtained prior to initiation of any study-specific procedure and treatment (by the subject or a legally acceptable representative as per the local regulations).
Written Informed Consent not obtained, signed and dated
Ability to provide signed Informed Consent Form
Be 18 years of age at the time the informed consent form is signed
Provide written informed consent prior to any study related procedure. (In the event that the patient is re-screened for study participation or a protocol amendment alters the care of an ongoing patient, a new informed consent form must be signed.)
Participant has signed informed consent form (ICF) before any trial related activities and according to local guidelines.
Be 18 years old at the time the informed consent form is signed
Signed informed consent form
Patient or authorized proxy needs to have signed the informed consent form
Signed Informed consent form
STUDY ENTRY: Signed Informed Consent Form (ICF).
Signed Informed Consent Form.
Signed informed consent form (ICF) and comply with the requirements of the study protocol
Signed informed consent form (ICF)
Signed informed consent form (ICF)
Signed informed consent form (ICF)
Signed informed consent form (ICF)
Subject has been informed of the study procedures and the treatment and has signed an informed consent form
Signed informed consent form in accordance with institutional policies prior to the initiation of high-dose therapy
Signed study-specific consent form
Signed informed consent form must be obtained prior to any research procedure
Have signed the current approved informed consent form
Signed written informed consent form
Informed consent form signed by the subject
Signed informed consent form must be obtained prior to any study procedure
Signed Informed Consent Form
Signed study-specific consent form prior to registration
Signed informed consent form
Signed informed consent form
Signed informed consent form
Subjects provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Signed informed consent form (ICF).
Signed informed consent form.
Patients must provide a signed informed consent form before any trial relates activities are carried out.
The patient must signed an informed consent form (ICF).
Signed informed consent form (ICF)
Voluntary signed informed consent form (ICF).
Signed study-specific consent form prior to registration
A signed informed consent form or minor assent form
A signed informed consent form or minor assent form
Signed informed consent form
Signed study specific informed consent form;
Patient has provided a signed study informed consent form prior to performance of any study related procedure
Signed study-specific consent form prior to registration
The signed informed consent form prior to the performance of any study related procedures that are not considered part of standard of care
Signed informed consent form
The patient has signed the study-specific informed consent form
Signed informed consent form
Signed informed consent form (ICF)
Patients who have not provided a signed informed consent form to participate in the study, obtained prior to the start of any protocol related activities.
Patients must give written informed consent; a copy of the signed informed consent form will be retained in the patient’s chart
A signed study specific consent form is required
Signed informed consent form (ICF)
Have signed an approved informed consent form for the study.
Signed Informed Consent Form (ICF)
Signed IRB approved Informed Consent Form (ICF).
Patient has been informed about the nature of the study, and has agreed to participate in the study, and signed the informed consent form prior to participation in any study-related activities
Patient has been informed about the nature of the study and has agreed to participate in the study and signed the informed consent form prior to participation in any study-related activities
Signed informed consent form (ICF)
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
Signed the informed consent form (ICF)
Patients must have a signed informed consent form prior to enrollment on study
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
Signed informed consent form (ICF)
Signed study-specific informed consent form
The signed informed consent form
Signed informed consent form
(Patient participation) Signed written informed consent form
Signed informed consent form
Signed informed consent form from patient
Provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Signed informed consent form
Subjects must have signed an approved consent form
Patients who have signed an approved informed consent form
Received and signed an informed consent form.
Signed informed consent form
Signed informed consent form.
Subjects must have received and signed an informed consent form.
Subjects must have received and signed an informed consent form.
Signed Informed Consent Form
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
Written informed consent must be obtained prior to any screening procedures
Subjects must provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) consent prior to performance of study-specific procedures or assessments and must be willing to comply with treatment and follow up \r\n* Note: informed consent may be obtained prior to start of the specified screening window\r\n* Note: procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study such as bone scan) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
Signed written informed consent obtained prior to performing any study procedure, including pre-screening and screening procedures.
Written informed consent prior to beginning specific protocol procedures, including expected cooperation of the patients for the treatment and follow-up, must be obtained and documented according to the local regulatory requirements
Ability to provide written informed consent which must be obtained prior to any screening procedures and according to local guidelines
Written informed consent must be obtained prior to any screening procedures other than procedures performed as part of standard of care.
Written informed consent must be obtained prior to any screening procedures and according to local guidelines
Signed informed consent obtained prior to any screening procedures
Written informed consent obtained prior to any study-specific procedures not considered part of routine medical care.
Written informed consent for screening and trial participation procedures including biological material transfer and handling.
Written informed consent obtained prior to any study-specific procedures not considered part of routine medical care
Written informed consent obtained prior to any study-specific procedures not considered part of routine medical care
Signed written informed consent obtained prior to study procedures
Written informed consent must be obtained prior to any screening procedures
Signed written informed consent obtained prior to study procedures
Written informed consent (or assent/ parental consent for minor subjects) prior to any screening procedures
Written informed consent obtained from the subject prior to performing any protocol-related procedures
signed written informed consent obtained prior to study procedures
Signed informed consent obtained prior to any screening procedures
Written informed consent obtained prior to any screening procedures
Written informed consent obtained prior to biopsies and blood samples
Written informed consent obtained prior to biopsies and blood samples
Written informed consent prior to beginning specific protocol procedures, including expected cooperation of the patients for the study treatment regimen and follow-up, must be obtained and documented according to the local regulatory requirements
Ability to provide written informed consent for the protocol must be obtained prior to any screening procedures; if consent cannot be expressed in writing, it must be formally documented and witnessed, ideally via an independent trusted witness
Signed written informed consent must be obtained prior to any study procedures.
Signed informed consent obtained prior to any screening procedures
Written informed consent for the protocol must be obtained prior to any screening procedures
PHASE I STUDY ELIGIBILITY CRITERIA:\r\nAbility of subject to understand and the willingness to sign a written informed consent document prior to any protocol related procedures, including screening evaluations
Signed informed consent obtained prior to any screening procedures
Written informed consent must be obtained prior to any screening procedures
Signed informed consent obtained prior to any screening procedures
Signed informed consent obtained prior to any screening procedures
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up; procedures conducted as part of the subject‘s routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
Written informed consent must be obtained from all patients prior to any study procedures
Written informed consent must be obtained prior to any procedures unless considered standard of care.
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up; procedures conducted as part of the subject's routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
Written informed consent obtained from subject prior to any protocol related procedures
Written informed consent must be obtained prior to any screening procedures and according to local guidelines
Written informed consent must be obtained prior to any screening procedures and according to local guidelines
Informed consent must be obtained from all subjects prior to beginning therapy
Signed written informed consent and assent forms (if applicable) must be obtained prior to any study procedures
Written informed consent must be obtained prior to any screening procedures
Written informed consent prior to beginning specific protocol procedures, including expected cooperation of the patients for the treatment and follow-up, must be obtained and documented according to the local regulatory requirements.
Written informed consent must be obtained and documented according to the local regulatory requirements prior to beginning specific protocol procedures;
written informed consent obtained prior to any study-related procedures.
Signed informed consent obtained prior to any screening procedures
Written informed consent must be obtained prior to any screening procedures
Informed consent must be obtained prior to study initiation
Subjects must provide written informed consent within one month prior to performance of study-specific procedures or assessments and must be willing to comply with treatment and follow up\r\n* Note: informed consent will be obtained after establishing the diagnosis of high risk, localized prostate cancer, and may be obtained prior to start of the specified screening window\r\n* Note: procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study such as bone scan) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
Written informed consent must be obtained prior to any study-related procedures
Written informed consent obtained prior to any screening procedures performed
Written informed consent obtained prior to any screening procedures
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up; procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
Informed consent must be obtained in writing for all patients prior to performing study/screening procedures and prior to registration into the study
Subjects must provide written informed consent prior to performance of study specific procedures or assessments, and must be willing to comply with treatment and follow up \r\n* Procedures conducted as a part of routine clinical management of the subject (e.g., blood count, imaging study) and obtained prior to signed informed consent may be utilized for screening or baseline purposes provided these tests are obtained as specified in the protocol)
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow up; procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up; procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
EXPANSION COHORT ONLY: Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up; procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol
Written informed consent must be obtained prior to any screening procedures
Signed written informed consent obtained prior to performing any study procedure, including screening procedures.
Patients must have a written informed consent obtained prior to the initiation of study procedures
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow up; procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol; Note: it is not necessary that informed consent be obtained within the protocol-specified screening window
Written informed consent has been obtained prior to the performance of any protocol-specific procedure.
Written informed consent has been obtained prior to the performance of any protocol-specific procedure.
Ability to provide written informed consent for the protocol must be obtained prior to any screening procedures; if consent cannot be expressed in writing, it must be formally documented and witnessed, ideally via an independent trusted witness
Written informed consent must be obtained prior to any procedures
Signed informed consent obtained prior to any screening procedures
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up; procedures conducted as part of the subject’s routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol \r\n* Note: it is not necessary that informed consent be obtained within the protocol specified screening window
Written informed consent must be obtained prior to any baseline/screening procedures.
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Written informed consent obtained prior to any study-related procedure being performed.
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Patient must have ability to understand and willingness to provide written informed consent prior to participation in the study and any related procedures being performed
Written informed consent obtained prior to any study-related procedure being performed;
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Able to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Written informed consent obtained prior to any study-related procedure being performed;
Subject must provide written informed consent prior to any study-related procedures being performed
Ability to provide written informed consent obtained prior to participation in the study
Voluntarily consents to participate and provides written informed consent prior to any protocol-specific procedures
Provide written informed consent prior to any study-specific screening procedures
Able to provide written informed consent prior to the performance of any study-specific procedures.
Provide written informed consent obtained prior to the initiation of study procedures
Patients must provide written informed consent prior to any study procedures
Provide written informed consent prior to study-specific screening procedures, with the understanding that the patient has the right to withdraw from the study at any time, without prejudice
The ability to provide written informed consent prior to study specific screening procedures, with the understanding that the patient has the right to withdraw from the study at any time
Provide written informed consent prior to any study-specific screening procedures.
The subject must sign a written informed consent form prior to the initiation of any study procedures. Adult subjects unable to provide written informed consent on their own behalf will not be eligible for the study
Provide written, informed consent to participate in the study and follow the study procedures
Willing and able to provide written informed consent prior to performance of any study-specific procedures
Be able to provide written, personally signed, and dated informed consent to participate in the study before completing any study-related procedures. As applicable, a parent/both parents or legally authorized representative (LAR) must provide signature of informed consent and there must be documentation of assent by the subject before completing any study-related procedures.
Be willing and able to provide written informed consent prior to initiation of any study procedures
Patients must provide written informed consent prior to any screening procedures
Provide written, informed consent to participate in the study and follow the study procedures
Ability to give written, informed consent prior to any study-specific screening procedures, with the understanding that the consent may be withdrawn by the patient at any time without prejudice.
Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures
Willing and able to provide written informed consent prior to initiation of any study-related procedures
Provide informed consent and agree to all assessments and study procedures
Patients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related procedures.
Written informed consent prior to any study-specific screening procedures with the understanding that the patient may withdraw consent at any time without prejudice
Written informed consent prior to initiation of any study-related procedures;
Must be willing to provide informed consent prior to any study specific procedures
The subject must be able to provide written, personally signed, and dated informed consent to participate in the study before completing any study-related procedures. As applicable, a parent/both parents or legally authorized representative (LAR) must provide signature of informed consent and there must be documentation of assent by the subject before completing any study-related procedures.
Subjects must provide a signed informed consent before any screening procedures
Patients must provide written informed consent prior to any screening procedures
Provide written, informed consent to participate in the study and follow the study procedures
Patients must provide written informed consent prior to any screening procedures
Following receipt of verbal and written information about the study, patients must provide signed informed consent before any study-related activity is carried out.
Provide written, informed consent to participate in the study and follow the study procedures
Ability to voluntarily provide informed consent to participate prior to any study-related assessments/procedures being conducted
Patients must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to adhere with treatment and follow-up
Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures
Patients must provide written informed consent prior to performance of study-specific procedures or assessments and must be willing to comply with treatment and follow-up
Provide written, informed consent to participate in the study and follow the study procedures
Written informed consent granted prior to initiation of any study-specific screening procedures, given with the understanding that the patient has the right to withdraw from the study at any time, without prejudice
Have given written informed consent prior to any study procedures
Provide signed informed consent after receipt of oral and written information about the study and before any study-related activity is performed
Patients must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to adhere with treatment and follow-up
Understands the potential risks and benefits of study participation and is willing to provide written informed consent.
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up
Subjects must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow up
Able to provide written informed consent prior to any study specific screening procedures with the understanding that the patient has the right to withdraw from the study at any time, for any reason without prejudice
Provide written informed consent prior to any study procedures.
Willing and able to provide written informed consent prior to performance of any study-specific procedures
Willing to adhere to protocol specific requirements 12. Following receipt of verbal and written information about the study, the subject must provide signed informed consent before any study related activity is carried out. 13. Clinically significant toxic effects of prior therapy (expect hydroxyuria) resolved to Grade ? 1 before the start of study.
Following receipt of verbal and written information about the study, patients must provide signed informed consent before any study-related activity is carried out.
Provide written informed consent prior to any screening procedures
Provide written informed consent prior to any screening procedures
Provide written informed consent prior to any study-specific procedures
Written informed consent prior to any study specific screening procedures with the understanding that the patient may withdraw consent at any time without prejudice
PATIENT EXCLUSION: Unable to provide informed consent or complete study procedures as determined by clinical or study staff
CAREGIVER EXCLUSION: Unable to provide informed consent or complete study procedures as determined by clinical or study staff
Patients must provide written informed consent prior to any screening procedures
Written informed consent prior to any study-related procedures
Written informed consent prior to any study-related procedures
Patients must provide written informed consent prior to any screening procedures
Provide informed consent and agree to all assessments and study procedures.
Provide informed consent and agree to all assessments and study procedures
Provide informed consent and agree to all assessments and study procedures
Patients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related procedures
Patients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related procedures
INCLUSION CRITERIA (NEXT 60 PATIENTS WITH LOCALLY ADVANCED PROSTATE CANCER): Patients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related procedures
Patients or their legal representatives must have the ability to read, understand and provide written informed consent for the initiation of any study related procedures
The subject must sign a written informed consent form prior to the initiation of any study procedures. Adult subjects unable to provide written informed consent on their own behalf will not be eligible for the study.
Provide written informed consent prior to any study-specific screening procedures
Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures
Understand and provide written informed consent prior to initiation of any study-specific procedures.
Provision of informed consent prior to any study specific procedures
Provision of informed consent
Provision of signed written informed consent
Provision of informed consent prior to any study specific procedures
Provision of written informed consent prior to any study-specific procedures
Provision of written informed consent
Provision of informed consent prior to any study specific procedures.
Provision of signed informed consent.
Provision of signed written informed consent.
Provision of genetics research informed consent
Provision of written informed consent to participate in this investigational study
Provision of informed consent prior to any study specific procedures
Provision of informed consent prior to any study specific procedures
Provision of informed consent prior to any study specific procedures
Provision of written informed consent
Provision of written informed consent prior to any screening procedures
The patient has a psychiatric illness or developmental delay that would interfere with understanding of the study and provision of informed consent
Provision of written informed consent
Provision of informed consent prior
Provision of informed consent prior to any study specific procedures.
Provision to sign and date the consent form
Provision of informed consent prior to any study specific procedures.
Provision of fully informed consent prior to any study specific procedures
Provision of informed consent prior to any study specific procedures
Provision of informed consent prior to any study specific procedures, sampling, and analysis.
Provision of informed consent prior to any study specific procedures, sampling and analyses.
Provision of written signed informed consent prior to any study specific procedures;
Provision of a signed informed consent
Provision of a signed informed consent
Provision of informed consent prior to any study specific procedures
Provision of written informed consent
Provision of written informed consent
Provision of informed consent
Provision of informed consent prior to any study-related procedures
Provision of written informed consent.
Provision of informed consent prior to any study-related procedures
Provision of written informed consent to participate in this investigational study
A willingness to follow the study protocol, as indicated by provision of informed consent to participate
Provision of written informed consent for tumor resection, stereotactic surgery, tumor biopsy, samples collection and treatment with investigational products prior to undergoing any study procedures
Provision of written informed consent and assent, when applicable, for tumor resection, stereotactic surgery, tumor biopsy, sample collection, and/or treatment with study drug prior to undergoing any study-specific procedures
Provision of informed consent by primary caregiver
Provision of informed consent
Provision to sign and date the consent form
Provision of informed consent prior to any study-related procedures
Provision of written informed consent
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA]) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization (applies to covered entities in the Unites States of America [USA] only) obtained from the subject/legal representative prior to performing any protocol-related procedures, including screening evaluations.
Written informed consent and authorization obtained from the subject/Health Insurance Portability and Accountability Act (HIPAA)-appointed legal representative prior to performing any protocol-related procedures including screening evaluations
Written informed consent obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent obtained from the patient/legal representative prior to performing any protocol-related procedures, including screening evaluation
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA]) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA]) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations.
Written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization obtained from the subject/legal representative prior to performing any protocol-related procedures
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
The patient/legal representative must be able to read and understand the informed consent form (ICF) and must have been willing to give written informed consent and any locally required authorization (eg, Health Insurance Portability and Accountability Act in the United States of America [USA]; European Union Data Privacy Directive in the European Union [EU]) before any study-specific procedures, including screening evaluations, sampling, and analyses
Written informed consent and any locally required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent must be obtained from the subject/legal representative prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA]) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of American [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Information Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g.,) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study; written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization will be obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA]) obtained from the patient prior to performing any protocol-related procedures, including screening evaluations
Signed written informed consent and Health Insurance Portability and Accountability Act (HIPAA) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent obtained from the patient/legal representative prior to performing any protocol-related procedures, including screening evaluations
Written informed consent by the patient (or legal representative) prior to admission to this study. In addition any locally required authorization (Health Insurance Portability and Accountability Act in the USA [HIPAA], obtained from the patient prior to performing any protocol-related procedures, including screening evaluations.
Written informed consent and any locally required authorization (eg, HIPAA) obtained from the patient/legal representative prior to performing any protocol-related procedures, including screening evaluations.
Written informed consent and authorization obtained from the subject/Health Insurance Portability and Accountability Act (HIPAA)-appointed legal representative prior to performing any protocol-related procedures including screening evaluations
Written informed consent and any locally-required authorization obtained from the patient prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and HIPAA authorization (applies to covered entities in the USA only) obtained from the subject/legal representative prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally required authorization (e.g., HIPAA in the USA) obtained from the patient/legal representative prior to performing any protocol-related procedures, including screening evaluations.
Written informed consent and any locally required authorization (eg, Health Insurance Portability and Accountability Act [HIPAA] in the USA) obtained from the subject/legal representative prior to performing any protocol-related procedures, including screening evaluations
Written informed consent and any locally-required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] authorization) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations
Provided informed consent
Provided written informed consent prior to any study-specific procedures.
Informed consent provided
Written informed consent provided prior to the initiation of study procedures
Written informed consent provided.
Provided written informed consent
Has provided written informed consent for participation in this trial
Subject has provided written informed consent
Subject has provided informed consent prior to initiation of any study-specific activities/procedures;
Have provided written informed consent
Must have provided written informed consent prior to participating in any study-related activity.
Have provided written consent for protocol directed biopsies
Have provided written informed consent.
Subject has provided informed consent
Has provided written informed consent prior to completing any study procedures
There will be no upper age limit for eligibility; elderly patients will be eligible for participation provided they are competent to provide informed consent, or written consent can be provided by their duly appointed healthcare proxy
Have provided informed consent
101 Subject has provided informed consent prior to initiation of any study-specific activities/procedures OR subject's legally acceptable representative has provided informed consent prior to any study-specific activities/procedures being initiated when the subject has any kind of condition that, in the opinion of the investigator, may compromise the ability of the subject to give written informed consent.
Written informed consent provided
Subject has provided informed consent prior to initiation of any study-specific activities/procedures
Provided written consent
Written informed consent provided
Written informed consent must be provided.
Must have provided informed consent for study participation.
Has provided written informed consent prior to any study related activities.
Subject has provided informed consent or subject's legally acceptable representative has provided informed consent when the subject has any kind of condition that, in the opinion of the Investigator, may compromise the ability of the subject to give written informed consent.
Written informed consent provided.
Has provided written informed consent
Subject has provided informed consent.
Has provided written informed consent
Patients will have provided informed consent to participate, documented by their signature on the study consent form
Subject must have provided written Informed Consent
Have been informed of the nature of the study and provided written informed consent, prior to initiation of any study activities;
Patients will have provided informed consent to participate, documented by their signature on the study consent form
Patients will have provided informed consent to participate, documented by their signature on the study consent form
Subject has provided written informed consent with HIPAA authorization
Patient having provided his/her written informed consent to participate in the trial prior to any study-related procedure being conducted
Subject has provided written informed consent to participate in the study
Subject has provided written informed consent to participate in the study
Has voluntarily consented to participate and provided written informed consent prior to any protocol-specific procedures
Patients who have provided informed consent for the long term follow up study prior to their study participation .
Subject's legally acceptable representative has provided informed consent/assent when the subject is legally too young to provide informed consent/assent and the subject has provided written assent based on local regulations and/or guidelines prior to any study-specific activities/procedures being initiated.