Signed informed consentXx_NEWLINE_xXSigned, dated informed consentXx_NEWLINE_xXVoluntary signed informed consent (IC)Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSigned and dated informed consentXx_NEWLINE_xXSubject has the ability to understand and provide signed informed consentXx_NEWLINE_xXProcurement: Informed consent explained to, understood by and signed by patient. Patient given copy of informed consentXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient. Patient given copy of informed consentXx_NEWLINE_xXAbility to understand the purpose and risks of the study and provide signed and dated informed consent.Xx_NEWLINE_xXSigned, written IRB-approved informed consentXx_NEWLINE_xXAbility to provide signed Informed Consent FormXx_NEWLINE_xXSigned informed consent prior to any proceduresXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatients must have signed an approved informed consentXx_NEWLINE_xXAbility to understand and the willingness to sign a written informed consent document; NOTE: consent documents can be signed up to 30 days prior to registration; if > 30 days has elapsed since patient signed the consent document, s/he must re-consent (new signature) before proceeding to register onto studyXx_NEWLINE_xXDated and signed IEC/IRB-approved informed consent.Xx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol and has signed the informed consent documentXx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXThe patient must be able to comprehend and have signed the informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll subjects must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSigned informed consent MUST be obtained from patient or parent/legal guardian (if patient is less than 18 years of age). Consent must be signed prior to any study procedures and study entryXx_NEWLINE_xXSigned informed consent/assentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol and has signed the informed consent documentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol and has signed the informed consent documentXx_NEWLINE_xXPatient has signed informed consentXx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXProvide 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.)Xx_NEWLINE_xXParticipant has signed informed consent form (ICF) before any trial related activities and according to local guidelines.Xx_NEWLINE_xXEvidence of a signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the studyXx_NEWLINE_xXPROCUREMENT INCLUSION CRITERIA: Informed consent explained to, understood by and signed by patient; patient given copy of informed consentXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient; patient given copy of informed consentXx_NEWLINE_xXINCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXINCLUSION - TREATMENT: Informed consent explained to, understood by, and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXSigned and dated written informed consentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol and has signed the informed consent documentXx_NEWLINE_xXSigned informed consent according to institutional guidelines must be obtainedXx_NEWLINE_xXBe 18 years old at the time the informed consent form is signedXx_NEWLINE_xXThe participant is capable of understanding and complying with the protocol and has signed the informed consent documentXx_NEWLINE_xXSigned informed consent for the study protocolXx_NEWLINE_xXINCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given a copy of informed consentXx_NEWLINE_xXINCLUSION - INFUSION: Informed consent explained to, understood and signed by patient/guardian; patient/guardian given a copy of informed consentXx_NEWLINE_xXAble to provide signed and dated informed consent before initiation of any study procedures.Xx_NEWLINE_xXSubject has signed and dated informed consentXx_NEWLINE_xXPROCUREMENT INCLUSION: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXTREATMENT INCLUSION: Informed consent explained to, understood by and signed by patient or guardian; patient or guardian given a copy of the informed consent formXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xX• Subject signed inform consentXx_NEWLINE_xXIn the opinion of the Investigator, the patient is capable of understanding and complying with the protocol and has signed the informed consent document.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned donor and patient/guardian informed consent;Xx_NEWLINE_xXPHASE I: Signed informed consentXx_NEWLINE_xXPHASE IB: Signed informed consentXx_NEWLINE_xXShow evidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial.Xx_NEWLINE_xXSubjects must be able to understand and be willing to sign the written informed consent form; ideally, a signed informed consent form will be appropriately obtained prior to the conduct of any trial-specific procedure; however, if patients have had standard of care assessments performed within the screening period, but before the consent was signed, these will be admissibleXx_NEWLINE_xXUnable to understand the purpose and risks of the study and to provide a signed and dated informed consent form (ICF)Xx_NEWLINE_xXELIGIBILITY CRITERIA AT TIME OF TREATMENT: Informed consent (and assent as applicable) signed by patient/guardianXx_NEWLINE_xXPROCUREMENT INCLUSION CRITERIA: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXFailure to provide signed informed consentXx_NEWLINE_xXPatient or authorized proxy needs to have signed the informed consent formXx_NEWLINE_xXAble to provide signed informed consent (or consent provided by legal guardian for pediatric patients, as applicable)Xx_NEWLINE_xXUnderstand study design, risks, and benefits and have signed informed consentXx_NEWLINE_xXINCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXINCLUSION - TREATMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXPatient has signed and dated informed consentXx_NEWLINE_xXThe patient must be competent and have signed informed consentXx_NEWLINE_xXAbility to sign an informed consent; can be signed by family member or health care proxy; informed consent must be done prior to registration on studyXx_NEWLINE_xXAll patients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSigned and dated written informed consent.Xx_NEWLINE_xXSigned and dated written informed consent.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned, informed consentXx_NEWLINE_xXAbility to understand the purpose and risks of the study and provide signed and dated informed consentXx_NEWLINE_xXSigned Informed consent formXx_NEWLINE_xXSigned and dated written informed consent obtained from patient or legal representative.Xx_NEWLINE_xXHave signed an informed consent document indicating that the subject understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXEvidence of a personally signed informed consent document.Xx_NEWLINE_xXWritten informed consent and/or signed assent from patient, parent or guardian.Xx_NEWLINE_xXSTUDY ENTRY: Signed Informed Consent Form (ICF).Xx_NEWLINE_xXSigned and dated informed consentXx_NEWLINE_xXCapable of understanding and complying with the protocol requirements and has signed the informed consent document.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXProvision of signed and dated informed consent form (ICF).Xx_NEWLINE_xXThe participant is capable of understanding and complying with the protocol and has signed the informed consent documentXx_NEWLINE_xXSigned Informed Consent Form.Xx_NEWLINE_xXSigned informed consent according to institutional guidelines must be obtained prior to registrationXx_NEWLINE_xXAbility 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 proceduresXx_NEWLINE_xXEvidence of a personally signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the studyXx_NEWLINE_xXSigned informed consent document and assent when appropriateXx_NEWLINE_xXHave signed an informed consent document indicating that the subject understands the purpose of and procedures required for the study and is willing to participate in the study.Xx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXSigned and dated written informed consentXx_NEWLINE_xXSubjects must be able and willingly give signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAbility to understand and provide signed informed consentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXSigned informed consent form (ICF) and comply with the requirements of the study protocolXx_NEWLINE_xXHave signed informed consent to participate in the studyXx_NEWLINE_xXSigned and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXProvision of signed informed consent.Xx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXParticipants signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXSubject has signed and dated informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatient must have the ability to understand the requirements of the study and signed informed consent. A signed informed consent by the patient or his legally authorized representative is required\r\nprior to their enrollment on the protocolXx_NEWLINE_xXCapable of understanding and complying with the protocol and has signed the informed consent documentXx_NEWLINE_xXSigned study-specific informed consentXx_NEWLINE_xXSigned, informed consentXx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXSigned informed consent;Xx_NEWLINE_xXSigned and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXPatient has the ability to understand and provide signed informed consentXx_NEWLINE_xXSigned informed consent;Xx_NEWLINE_xXProvide signed Informed ConsentXx_NEWLINE_xXSigned consent to long-term follow-up protocol PA17-0483.Xx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXThe patient is capable of understanding and complying with the protocol and has signed the informed consent document. A signed informed consent form must be obtained before any study-specific procedures are performed.Xx_NEWLINE_xXSigned and dated written informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated written informed consent prior to admission to the studyXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXInformed consent signed by the subjectXx_NEWLINE_xXSubject has been informed of the study procedures and the treatment and has signed an informed consent formXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXCapability to understand and comply with the protocol requirements as and signed informed consent documentsXx_NEWLINE_xXCapable of giving signed informed consentXx_NEWLINE_xXSigned informed consent document(s)Xx_NEWLINE_xXSigned informed consent form in accordance with institutional policies prior to the initiation of high-dose therapyXx_NEWLINE_xXHave signed an informed consent document indicating that the subject understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXSigned and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXSigned informed consent on protocol LAB02-188Xx_NEWLINE_xXHave signed an informed consent documentXx_NEWLINE_xXSigned informed consent by patient and/or parents or legal guardianXx_NEWLINE_xXEvidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the studyXx_NEWLINE_xXPRIOR TO LYMPHODEPLETION: Informed consent explained to, understood by and signed by the patient or legal guardian for pediatric patients; patient and/or legal guardian given a copy of informed consent formXx_NEWLINE_xXSigned, informed consentXx_NEWLINE_xXSigned informed consent according to institutional guidelines prior to registration.Xx_NEWLINE_xXInformed consent obtained and signedXx_NEWLINE_xXSigned and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollment.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent form must be obtained prior to any research procedureXx_NEWLINE_xXInformed consent reviewed and signedXx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXSigned consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXHave signed the current approved informed consent formXx_NEWLINE_xXWritten informed consent from patient and/or signed assent from patient, parent or guardianXx_NEWLINE_xXSigned written informed consent formXx_NEWLINE_xXAbility to understand and provide signed informed consentXx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXSubject understood and signed the study specific informed consentXx_NEWLINE_xXAT THE TIME OF PROCUREMENT: Informed consent explained to, understood by and signed by subject/guardian; subject/guardian given copy of informed consentXx_NEWLINE_xXAT THE TIME OF INFUSION: Informed consent explained to, understood by and signed by research subjects/guardian; subject/guardian given copy of informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPROCUREMENT: Informed consent explained to and signed by patient/guardian able to give informed consent and patient given a copyXx_NEWLINE_xXTREATMENT: Informed consent explained to and signed by patient/guardian able to give informed consent and patient given a copyXx_NEWLINE_xXSigned and dated informed consent form indicating that the patient has been informed of all pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXPatient has signed informed consent and is willing to comply with the protocolXx_NEWLINE_xXCapable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXPatient has the ability to understand and provide signed informed consentXx_NEWLINE_xXInformed consent form signed by the subjectXx_NEWLINE_xXA signed and dated written informed consent form is obtained from the subjectXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian. Patient/guardian given copy of informed consent.Xx_NEWLINE_xXAbility to understand and provide signed informed consentXx_NEWLINE_xXWritten informed consent and/or signed assent line from patient, parent or guardianXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and witnessed informed consent and signed authorization for the release of their protected health informationXx_NEWLINE_xXPatient must have the ability to understand the requirements of the study and signed informed consent a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocolXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXWritten informed consent and/or signed assent line from patient, parent or guardianXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXSigned informed consent form must be obtained prior to any study procedureXx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll patients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXPatients must have signed an approved informed consentXx_NEWLINE_xXSigned informed consent document(s)Xx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated written informed consentXx_NEWLINE_xXPatient (if ? 18 years old), or patient's legal representative(s) must have signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatient has signed the informed consent document agreeing to the use of the study drug, domperidoneXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated written informed consentXx_NEWLINE_xXInformed consent obtained and signedXx_NEWLINE_xXPatient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocolXx_NEWLINE_xXPatients must have signed an approved informed consentXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXInformed consent explained to, understood and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXPatient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocolXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXProvided signed informed consent.Xx_NEWLINE_xXSigned written pre-registration informed consent documentXx_NEWLINE_xXSigned written informed consent\r\n* The signed informed consent\r\n* The benefits/risks of the induction chemotherapy regimen will be reviewed, and a second consent may be necessary if the regimen will be administered according to a separate protocolXx_NEWLINE_xXSigned informed consent according to institutional guidelines must be obtainedXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent by the patient or legally authorized representativeXx_NEWLINE_xXWritten informed consent and/or signed assent line from patient, parent or guardianXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXInformed Consent: Signed by the subject prior to screening.Xx_NEWLINE_xXConsent signedXx_NEWLINE_xXPART II: The Part 2 consent must be signedXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXProvide signed informed consentXx_NEWLINE_xXSigned informed consent before initiation of any study procedures.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated informed consent of the patient, available before the start of any specific trial procedure.Xx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatients must have voluntarily signed an informed consent in accordance with institutional policies.Xx_NEWLINE_xXAll patients must have given a signed, informed consent prior to enrollment on studyXx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXPatients who have signed informed consent for this long term extension program.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSubjects provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.Xx_NEWLINE_xXSigned and dated informed consent document.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXCapable of giving signed informed consent.Xx_NEWLINE_xXSigned consent to long-term follow- up protocol PA17- 0483Xx_NEWLINE_xXSigned informed consent form (ICF).Xx_NEWLINE_xXSigned informed consent on protocol LAB02-188.Xx_NEWLINE_xXSigned and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the trial prior to randomizationXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXENROLLMENT: Signed informed consent and if applicable pediatric assent.Xx_NEWLINE_xXSigned informed consent form.Xx_NEWLINE_xXPatient has signed the informed consent form prior to the performance of any screening procedures and is able to comply with protocol requirements.Xx_NEWLINE_xXSigned informed consent for protocol PA13-0291Xx_NEWLINE_xXPatient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocolXx_NEWLINE_xXPatient has signed the Informed Consent Form (ICF) prior to any screening procedures being performed and is able to comply with protocol requirementsXx_NEWLINE_xXInformed consent document signed and dated by patientXx_NEWLINE_xXPatients must provide a signed informed consent form before any trial relates activities are carried out.Xx_NEWLINE_xXProvide signed informed consentXx_NEWLINE_xXThe patient must signed an informed consent form (ICF).Xx_NEWLINE_xXSigned & dated informed consent prior to Screening evaluationsXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXSubjects must provide a signed informed consent before any screening proceduresXx_NEWLINE_xXPatient has signed the informed consent (ICF) prior to any screening procedures being performed and is able to comply with protocol requirementXx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXSigned informed consent for the focal laser ablation (FLA) treatment through the 12 month follow up visitXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAble to provide signed, informed consentXx_NEWLINE_xXSigned informed consent according to institutional guidelines must be obtainedXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAbility to understand and sign the informed consent; patient must have signed informed consent prior to registration on studyXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXSigned and informed consent to participant in this studyXx_NEWLINE_xXSigned informed consent to participate in this studyXx_NEWLINE_xXPatients must have signed an approved informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent by the patient or the patient's parent or guardian for patients who are minorsXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXCapable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXSigned and dated written informed consent to participate in this clinical trial must be obtained prior to any study procedureXx_NEWLINE_xXPatient is willing to participate in the study and has signed the study informed consentXx_NEWLINE_xXSigned, written IRB-approved informed consent.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatients must have signed an approved informed consentXx_NEWLINE_xXVoluntary signed informed consent form (ICF).Xx_NEWLINE_xXSigned study-specific informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXA signed informed consent form or minor assent formXx_NEWLINE_xXProvide signed and dated informed consent indicating that the patient has been informed of all pertinent aspects of the study, including the potential risks, and is willingly participating.Xx_NEWLINE_xXThe patient must signed an informed consent form indicating that she/he understands the purpose of and procedures required for the study and is willing to participate in the study.Xx_NEWLINE_xXSigned informed consent prior to any study-related evaluationXx_NEWLINE_xXA signed informed consent form or minor assent formXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned study specific informed consent form;Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatient has provided a signed study informed consent form prior to performance of any study related procedureXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated informed consent.Xx_NEWLINE_xXThe signed informed consent form prior to the performance of any study related procedures that are not considered part of standard of careXx_NEWLINE_xXSigned informed consent documentXx_NEWLINE_xXInformed consent explained to and signed by patient or parent/guardian able to give informed consent and given a copyXx_NEWLINE_xXInformed consent explained to and signed by patient or parent/guardian able to give informed consent and given a copyXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXParticipant is able to provide signed informed consentXx_NEWLINE_xXCapable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXBe 18 years old at the time the informed consent is signedXx_NEWLINE_xXAbility to understand the purpose of the study, provide signed and dated informed consent, and able to comply with all proceduresXx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll patients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXAll subjects must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXCapable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXPatient provides signed and dated informed consent prior to initiation of any study procedures.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXThe patient has provided signed informed consentXx_NEWLINE_xXThe patient has signed the study-specific informed consent formXx_NEWLINE_xXSigned and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXMust provide a signed and dated informed consent indicating that the participants has been informed of all pertinent aspects of the study, including the potential risks, and is willingly participating.Xx_NEWLINE_xXProvision of signed and dated, written informed consentXx_NEWLINE_xXAT THE TIME OF PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXAT THE TIME OF INFUSION: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consentXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXPatient has the ability and willingness to provide informed consent and has signed the informed consent documentXx_NEWLINE_xXHave signed an informed consent document indicating that the subjects understand the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXInformed consent reviewed and signedXx_NEWLINE_xXHave signed an informed consent document indicating that the subjects understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXPatient has signed a written informed consent.Xx_NEWLINE_xXProvide signed informed consentXx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXSigned and dated informed consent.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXHas provided a signed informed consentXx_NEWLINE_xXHave signed an informed consent document indicating that the subjects understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll patients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSigned Informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXHave signed an informed consent document indicating that the subjects understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll patients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSTEP 2 ENROLLMENT AND RANDOMIZATION: the patient has signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatients must have signed an approved informed consentXx_NEWLINE_xXSigned a protocol-specific informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned study-specific informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent from patients and/or their parents or legal guardiansXx_NEWLINE_xXThe participant is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXPatients who have not provided a signed informed consent form to participate in the study, obtained prior to the start of any protocol related activities.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXHas provided signed informed consent for this study.Xx_NEWLINE_xXAn approved informed consent must be signed by the patientXx_NEWLINE_xXSigned informed consent from patients and/or their parents or legal guardiansXx_NEWLINE_xXSigned informed consent documentXx_NEWLINE_xXAll subjects must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSigned informed consent by patient and/or parents or legal guardianXx_NEWLINE_xXVoluntarily signed informed consent.Xx_NEWLINE_xXSigned Informed ConsentXx_NEWLINE_xXSigned and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to undergoing study screening proceduresXx_NEWLINE_xXHas provided signed informed consent for this study.Xx_NEWLINE_xXPatients must give written informed consent; a copy of the signed informed consent form will be retained in the patient’s chartXx_NEWLINE_xXSigned and dated IRB/Approved Informed ConsentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned study-specific informed consentXx_NEWLINE_xXSigned written informed consent to Study ARQ 197-299Xx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXSigned informed consent document and assent when appropriateXx_NEWLINE_xXThe patient must consent to be in the study and must have signed an approved consent form conforming to institutional guidelinesXx_NEWLINE_xXSigned informed consent according to institutional guidelines must be obtainedXx_NEWLINE_xXPatients who have signed an approved Informed ConsentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXHave signed an approved informed consent form for the study.Xx_NEWLINE_xXAble to provide signed and dated informed consent prior to initiation of any study procedures.Xx_NEWLINE_xXSigned Informed Consent Form (ICF)Xx_NEWLINE_xXProvision of a signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXProvision of a signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent prior to the start of systemic therapy; in the event of enrollment of a minor patient, an attempt to obtain assent from the patient must be documented, and parental consent must be signedXx_NEWLINE_xXSigned and dated written informed consent prior to admission to the studyXx_NEWLINE_xXSigned IRB approved Informed Consent Form (ICF).Xx_NEWLINE_xXSigned, approved Informed Consent.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSubject has signed and dated informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatient 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 activitiesXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXPatient 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 activitiesXx_NEWLINE_xXProcurement consent signed and faxed to Research CoordinatorXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatient must have signed informed consent prior to registration on this studyXx_NEWLINE_xXSigned and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXTREATMENT: Patients must have signed the screening consentXx_NEWLINE_xXPatients must have signed an approved informed consentXx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXPatients must have signed an approved informed consent.Xx_NEWLINE_xXPatient must provide a signed and dated written informed consent prior to registration and any study-related proceduresXx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXHave signed an informed consent document indicating that the subject understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXPRE-REGISTRATION INCLUSION CRITERIA: Signed and dated informed consent document for study participationXx_NEWLINE_xXEvidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trialXx_NEWLINE_xXInformed consent explained to, understood by and signed by patient/guardian. Patient/guardian given copy of informed consent.Xx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXVoluntarily signed and dated written informed consentXx_NEWLINE_xXVoluntarily signed and dated written informed consentXx_NEWLINE_xXSigned the informed consent form (ICF)Xx_NEWLINE_xXEvidence of a personally signed and dated written informed consent to participate in the clinical studyXx_NEWLINE_xXHave signed an informed consent document indicating that the subject understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatients must have a signed informed consent form prior to enrollment on studyXx_NEWLINE_xXSubjects, or subject's legal representative, who have provided signed informed consent, and assent when applicable, prior to participation.Xx_NEWLINE_xXUnable to give signed informed consentXx_NEWLINE_xXSigned informed ConsentXx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXSigned informed consent from patientXx_NEWLINE_xXInformed consent obtained and signedXx_NEWLINE_xXA signed informed consent document (ICD)Xx_NEWLINE_xXPatient (or legal representative) is able to understand and provide signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXSigned informed consent documentXx_NEWLINE_xXSigned Informed Consent.Xx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXWritten informed consent and/or signed assent line from patient, parent or guardianXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent form (ICF)Xx_NEWLINE_xXSigned study-specific informed consent formXx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXHave signed an informed consent document indicating that the subjects understands the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXThe signed informed consent formXx_NEWLINE_xXVoluntarily signed and dated written informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll patients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXThe subject has the capability of understanding the informed consent document and has signed the informed consent documentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXInformed consent explained to and signed by parent/legal guardian or patient if the patient is >= 18 yearsXx_NEWLINE_xXPatient or legal guardian has signed informed consent.Xx_NEWLINE_xXParents or legal guardian signed-written informed consentXx_NEWLINE_xXPatient and/or legal guardian able to provide signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned and dated written informed consentXx_NEWLINE_xXSigned and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollmentXx_NEWLINE_xXA personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXWritten informed consent (IC) for trial participation must be signed and dated by the patient and the investigator prior to enrollmentXx_NEWLINE_xXSigned ICFXx_NEWLINE_xXSigned and dated Informed Consent Form (by the patient or a legally acceptable representative as per the local regulations).Xx_NEWLINE_xXHave signed an informed consent document indicating that the subjects understand the purpose of and procedures required for the study and are willing to participate in the studyXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXCapable of giving signed, written informed consentXx_NEWLINE_xXAll patients will have given signed, informed consent prior to registrationXx_NEWLINE_xX(Patient participation) Signed written informed consent formXx_NEWLINE_xXPatient must provide signed informed consent.Xx_NEWLINE_xXProvide signed and dated informed consent formXx_NEWLINE_xXSigned informed consent to the studyXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXHave read and signed study informed consent document (ICF)Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll participants must have given signed, informed consent prior to registration in studyXx_NEWLINE_xXUnderstands study design, risks, and benefits and have signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXHas signed consent within 6 months of diagnosis dateXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXWritten informed consent form signed and dated by the subjectXx_NEWLINE_xXPatient aged 12-17 years: has signed informed assent and their parent/legal guardian has signed informed consent for study participationXx_NEWLINE_xXPatient aged 18-25 years: has signed informed consent for study participationXx_NEWLINE_xXAble to understand and comply with the protocol requirements and has signed the informed consent document.Xx_NEWLINE_xXSigned informed consent on protocol LAB02-188Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent`Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent form from patientXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXWritten informed consent and/or signed assent line from patient, parent or guardianXx_NEWLINE_xXSigned and dated informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned written informed consent by parent(s)/legal guardians of the pediatric patient in compliance with the local laws and regulations. In addition signed children's assent form according to local requirements.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXInformed consent explained to, understood by and signed by subject/guardian; subject/guardian given copy of informed consentXx_NEWLINE_xXAll patients must have given signed, informed consent prior to registration on studyXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned the 2 year extension study informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXParticipant is able and willing to comply with study procedures, and signed and dated informed consent is obtainedXx_NEWLINE_xXSigned and dated written IRB approved informed consent;Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXEvidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trialXx_NEWLINE_xXSigned informed consent obtained prior to any screening proceduresXx_NEWLINE_xXProvide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.Xx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned informed consent obtained prior to any screening procedureXx_NEWLINE_xXSigned document of informed consent completed by the parent or legal guardianXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXAll subjects must have given signed, informed consent prior to study registrationXx_NEWLINE_xXFor patients at high risk for developing aGVHD, informed consent should be signed prior to transplant.Xx_NEWLINE_xXProvide signed and dated informed consent formXx_NEWLINE_xXAbility to provide signed informed consent and willingness to comply with protocol requirementsXx_NEWLINE_xXInformed consent must be given and signedXx_NEWLINE_xXWillingness to signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXSigned, informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXInformed consent or assent signed by study subject or parent/guardian according to institutional guidelinesXx_NEWLINE_xXPatients must have signed informed consentXx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXProvide signed and dated informed consent form.Xx_NEWLINE_xXSubjects must have signed an approved consent formXx_NEWLINE_xXHave signed informed consent to participate in the studyXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXThe subject is capable of understanding and complying with the protocol requirements and has signed the informed consent documentXx_NEWLINE_xXSigned written informed consent and willingness to comply with protocol requirementsXx_NEWLINE_xXPatient has signed the informed consent (ICF) and is able to comply with protocol requirementsXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXPatients with signed informed consentXx_NEWLINE_xXSigned informed consentXx_NEWLINE_xXHave signed Informed Consent to participate in the studyXx_NEWLINE_xXSigned consentXx_NEWLINE_xXSigned consentXx_NEWLINE_xXPatients who have signed an approved informed consent formXx_NEWLINE_xXHave signed informed consent to participate in the studyXx_NEWLINE_xXSigned informed consent of the patientXx_NEWLINE_xXPatients must have signed an informed consentXx_NEWLINE_xXParticipants must be willing to participate and provide signed informed consentXx_NEWLINE_xXgive signed informed consent prior to the initiation of therapyXx_NEWLINE_xXSigned informed consent for patient’s participating in the paper based surveyXx_NEWLINE_xXReceived and signed an informed consent form.Xx_NEWLINE_xXSigned informed consent formXx_NEWLINE_xXThe patient is capable of understanding and complying with the protocol and has signed the informed consent document.Xx_NEWLINE_xXSigned informed consent form.Xx_NEWLINE_xXSubjects must have received and signed an informed consent form.Xx_NEWLINE_xXVoluntarily signed and dated informed consentXx_NEWLINE_xXPatient has the ability to understand and provide signed informed consent.Xx_NEWLINE_xXSigned informed consent.Xx_NEWLINE_xXSubjects must have received and signed an informed consent form.Xx_NEWLINE_xXSigned Informed Consent FormXx_NEWLINE_xXWritten Informed Consent not obtained, signed and datedXx_NEWLINE_xXBefore the patient is enrolled, the consent form, including any addenda, must be signed and dated by the patient and the person who explains the study to that patientXx_NEWLINE_xX