Able to understand and comply with the study procedures, understand the risks involved in the study, and provide written informed consent before the first study-specific procedure; specifically able to comply with the PK assessment schedule during the first 2 treatment cycles.
Subject is able to understand and willing to sign the ICF, according to institutional standards, prior to the initiation of any study related procedures;
Able to understand the study procedures and agree to participate in the study by providing written informed consent
Understand study design, risks, and benefits and have signed informed consent
Is able to provide written informed consent (in English) to participate in the study and able to understand the procedures and study requirements
Participants must be able to understand and sign a written informed consent form and understand the importance of adherence to study treatment and protocol; in addition, participants must demonstrate a willingness to follow all study requirements, including the concomitant medication restrictions, throughout the study
Patients must give written informed consent prior to initiation of therapy, in keeping with the policies of the institution. Patients with a history of major psychiatric illness must be judged able to fully understand the investigational nature of the study and the risks associated with the therapy.
Patients must give written informed consent prior to initiation of therapy, in keeping with the policies of the institution. Patients with a history of major psychiatric illness must be judged able to fully understand the investigational nature of the study and the risks associated with the therapy
Subject must understand risks and benefits of the protocol and be able to give informed consent
Able to understand and comply with the study procedures, understand the risks involved in the study, and provide written informed consent before the first study-specific procedure
Patient or legally appropriate proxy must be able to understand study instructions and sign consent
Able to understand, and the willingness to give, informed consent for the study
Patients must give written informed consent prior to initiation of therapy, in keeping with the policies of the institution; patients with a history of major psychiatric illness must be judged able to fully understand the investigational nature of the study and the risks associated with the therapy
Able to read or understand and give informed consent.
The patient, or their representative, is able to understand the study and is willing to consent to participation in the study.
Part 1: be able to understand the description of the study and give written informed consent
Part 2: able to understand the recommendations for participation in the study
Able to understand and comply with the protocol and study procedures, understand the risks involved in the study, and provide written informed consent before any study-specific procedure is performed.
Subjects must be able to understand the potential risks and benefits of the study, and be able to read and give written informed consent
Be able to understand the study procedures, agree to participate in the study program, and voluntarily provide written Informed Consent
Subjects must be able to understand the potential risks and benefits of the study and must be able to read and provide written, informed consent for the study
Subjects must be able to understand the potential risks and benefits of the study and must be able to read and provide written, informed consent for the study
Must be able to read and understand informed consent
Patients must be female, be ? 18 years of age, be able to understand the study procedures, and agree to participate in the study by providing written informed consent.
Able to understand the study procedures and agree to participate in the study by providing written informed consent Cohort Specific Inclusion Criteria:
Subjects willing and able to give written informed consent to participate in the study and to adhere to the procedures stated in the protocol, or legally acceptable representative willing and able to give written informed consent on behalf of the subject for minors, unconscious adults and those incapable of consenting themselves due to their medical condition, or included as permitted by local regulatory authorities, IRB/IECs or local laws.
Subject is able to read, understand, and sign a written Informed Consent to participate in the study.
Able to understand the description of the study and willing to participate
YBCS: Able to consent to the study
HCP: Able to consent to the study
Able to understand the description of the study and willing to participate
Be able to understand the description of the study and give written informed consent
Patient has been informed of the investigational nature of this study and has given written Informed Consent and is able to adhere to dosing and visit schedules and meet all study requirements
Able to fully understand and participate in the informed consent process
Patients who are able to understand and give consent to participating in the study
Patient is able to understand and give consent to participation in the study.
Patients who in the judgment of the investigators and/or consenting professional, are able to understand the purpose of the study and provide informed consent will be included
Able to understand study requirements
Unwilling or unable to provide informed consent; only individuals (aged 18 or over) who can understand and give informed consent will be approached to participate in this study; individuals who are considered to be mentally disabled will not be recruited for this study; all subjects must understand and be able to give informed consent; we will not be using specific methods to assess decisional capacity; economically disadvantaged persons will not be vulnerable to undue influence, as this study offers no compensation; all individuals will be told that their choice regarding study participation will in no way change their access to clinical care; this should negate any undue influence or coercion; children, fetuses, neonates, or prisoners\r\nare not included in this research study; the menopausal status of the study participant will be reviewed during the screening process by examining the patient’s chart, women of childbearing potential will have a serum or urine pregnancy test at the time of screening
Only individuals (aged 18 or over) who can understand and give informed consent will be eligible to participate in this study
Only individuals who can understand and give informed consent will be eligible to participate in this study
Adults with a suspected or confirmed lymphoma diagnosis and:\r\n* Who will undergo clinically indicated procedure potentially allowing for excess or discarded clinical specimens\r\n* Who must be able to understand and sign an informed consent
Inability to understand the risks and benefits of the study
Able to understand and comply with study procedures, understand the risks involved, and provide written informed consent.
Only individuals who can understand and give informed consent will be eligible to participate in this study; individuals who are considered to be mentally disabled will not be recruited for this study; all subjects must understand and be able to give informed consent; we will not be using specific methods to assess decisional capacity; all individuals will be told that their choice regarding study participation will in no way change their access to clinical care; this should negate any undue influence or coercion; children, fetuses, neonates, or prisoners are not included in this research study; women of child-bearing potential will have a urine pregnancy test at the time of screening
The patient must be able to communicate and understand/complete forms/instructions, and be able to provide informed written consent prior to enrollment; patients may have the assistance of an interpreter or surrogate when completing forms/surveys as needed
Participant must be able to understand and give consent to participate in the study
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Patient able to understand, sign, and date the written informed consent form at screening visit prior to any protocol-specific procedures
Understands and is willing to sign an informed consent form (ICF) prior to initiation of any study-specific procedure.
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure; subjects must be willing and able to comply with scheduled visits, treatment schedule, laboratory testing, and other study requirements
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Subjects 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 admissible
Each patient must be willing to participate as a research participant and must sign an informed consent form.
Sign an Informed Consent Form (ICF);
Patient able to understand and willing to sign and date the written voluntary informed consent form (ICF) at screening visit prior to any protocol-specific procedures
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure; subjects must be willing and able to comply with scheduled visits, treatment schedule, laboratory testing, and other study requirements
Patient must sign a study specific informed consent form
All patients must sign a study-specific consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Patients must be able to understand and be willing to sign the written informed consent form
Patients must sign a study-specific consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Sign Subject Information Sheet and Informed Consent Form
Able to understand and then sign an informed consent form (ICF) prior to initiation of any study-specific procedure and treatment.
Subjects must be able to understand and be willing to sign the written informed consent form
Patient is able to understand and is willing to sign the informed consent form
Must sign the picture consent form
All subjects must have the ability to understand and the willingness to sign a written informed consent\r\n* Note: For research participants who do not speak English, a short form consent may be used with a COH certified interpreter/translator to proceed with screening and leukapheresis, while the request for a translated full consent is processed; however, the research participant is allowed to proceed with lymphodepletion and T cell infusion only after the translated full consent form is signed
Sign a written informed consent form
Each patient much be willing to participate as a research subject and must sign an informed consent form
Each patient must be willing to participate as a research subject and must sign an informed consent form
Able to understand and sign a written informed consent form
Patient must give informed consent and sign an approved consent form prior to any study procedures.
Willing and able to understand and sign the study specific Informed Consent Form
Patient able to understand, sign, and date the written voluntary informed consent form at screening visit prior to any protocol-specific procedures
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Be able to understand and willing to sign an informed consent form (ICF).
Patient able to understand and willing to sign and date the written voluntary informed consent form (ICF) at screening visit prior to any protocol-specific procedures
The patient must sign an informed consent form (ICF)
Must sign study-specific consent form
Participants must sign an approved informed consent form (ICF).
Patients must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
All participating patients must exercise informed voluntary consent and sign a consent form approved by the University of Minnesota Committee on the Use of Human Subjects in Research
Patients must have the ability to sign an approved informed consent form (ICF).
Subjects must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.
Patients must sign a study-specific consent form
Able to understand and willing to sign the informed consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
The subject must sign and date all informed consent statements; children will sign the assent form and their guardian will sign the consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Able to understand and willing to sign informed consent form (ICF)
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Patient must sign a study-specific consent form prior to registration
Willing and able to understand and sign informed consent form
Subjects unable to review and sign informed consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Patient is aware of her diagnosis, understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Subjects or their guardians must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.
Each patients must be willing to participate as a research subject and must sign an informed consent form
Patients must sign a study-specific informed consent form
Patient must be willing and able to sign the informed consent form
Patients must sign a study-specific consent form
Patients must sign the informed consent form before registration
Each patient must be willing to participate as a research subject and must sign an informed consent form
Written informed consent provided before any study-specific procedures are initiated. Subject must be able to understand and be willing to sign a written informed consent form.
Must sign an informed consent form.
Each patient must be willing to participate as a research subject and must sign an informed consent form
Patients must sign a study-specific informed consent form prior to treatment
Each patient must be willing to participate as a research subject and must sign an informed consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Able to understand and willing to sign the informed consent form
Able to understand and sign a consent form
Patients must sign an informed consent form
Patient able to understand and willing to sign and date the written voluntary informed consent form (ICF) at screening visit prior to any protocol-specific procedures
Able to understand and willing to sign the informed consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Each patient must be willing to participate as a research subject and must sign an informed consent form
Patients of their legal representatives must be able to understand and sign an informed consent form
Able to understand and willing to sign an informed consent form (ICF) prior to initiation of any study-specific procedure and treatment
Must sign an Informed Consent Form (ICF)
Each patient must be willing to participate as a research subject and must sign an informed consent form
The patient must be able to understand the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
Patients must sign a study-specific consent form
Patient understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
Able and willing to sign protocol consent form
Patient understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
Inability to sign an informed consent form prior to registration on study
Capacity to understand and sign the study informed consent form
Willing and able to read, understand and sign an informed consent form (ICF)
Willing and able to understand and sign consent form
Patients must sign a study-specific consent form
Patient is able to sign a study specific informed consent form
Willing and able to sign consent form.
Patients must sign an informed consent form for study
Understands the trial and procedure and is willing and able to sign the informed consent form
Patient understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
Subject must be willing and able (in the opinion of the investigator) to understand the informed consent form
Subjects must be able to understand and willing to sign a written informed consent form
Sign an approved informed consent form for this study.
The subject or subject's medical power of attorney has provided written consent to participate in this study.
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Ability to understand and willing to provide informed consent\r\n* If patient unable to understand informed consent, a previously designated durable power of attorney for healthcare or an individual with legal authority may substitute in this capacity\r\n* Assignment of a durable power of attorney for healthcare if not already done
Willing to sign a durable power of attorney.
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Patient or durable power of attorney (DPA) for healthcare must be able to understand and voluntarily sign an Institutional Review Board (IRB) -approved informed consent form
All participants >= 18 years of age must be willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Patients must have the ability to understand the study, its risks, side effects, potential benefits and be able to give written informed consent to participate. Patients may not be consented by a durable power of attorney (DPA).
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Durable power of attorney form offered (patients >= 18 years of age only)
Willing to sign a durable power of attorney
All patients or their legal guardians (if the patient is < 18 years old) or durable power of attorney (DPA) must sign a document of informed consent indicating their understanding of the investigational nature and the risks of this study; when appropriate, pediatric patients will be included in all discussions in order to obtain verbal assent
Ability of patient or durable power of attorney (DPA) for healthcare to give informed consent
Patients must have the ability to understand the study, its risks, side effects, potential benefits and be able to give written informed consent to participate. Patients may not be consented by a durable power of attorney (DPA).
Patients must have the ability to understand the study, its inherent risks, side effects and potential benefits and be able to give written informed consent to participate. Patients may not be consented by a durable power of attorney (DPA).
Patients must have the ability to understand the study, its risks, side effects, potential benefits and be able to give written informed consent to participate. Patients may not be consented by a durable power of attorney (DPA).
Patient or designated individuals with durable medical power of attorney must give written informed consent prior to any study-specific procedures being implemented
Willing to sign a durable power of attorney
Patients must have the ability to understand the study, its inherent risks, side effects and potential benefits and be able to give written informed consent to participate. Patients may not be consented by a durable power of attorney (DPA).
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Durable power of attorney form offered (patients >= 18 years of age only)
Willing to sign a durable power of attorney
Willing to sign durable power of attorney
Willing to sign a durable power of attorney
Patient or durable power of attorney (DPA) for healthcare must be able to understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
Willing to sign a durable power of attorney
Willing to sign a durable power of attorney
Must be able to understand and voluntarily sign an informed consent form (ICF).
Subjects must voluntarily sign an informed consent form (ICF); and able to meet all study requirements
Able to understand and voluntarily sign an informed consent form
Subject must understand and voluntarily sign an Informed Consent Form (ICF) prior to any study-specific assessments/procedures being conducted.
Must be able to understand and voluntarily sign an informed consent form (ICF).
Able to understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form.
Able to understand and voluntarily sign an informed consent form
Willing and able to understand and voluntarily sign a written informed consent
Understand and voluntarily sign an informed consent document
Subject (when applicable, parental/legal representative) must understand and voluntarily sign an ICF/IAF prior to any study-related assessments/procedures being conducted.
Understand and voluntarily sign an informed consent, and be able to comply with study procedures and follow-up examinations.
Understand and voluntarily sign an informed consent document prior to conducting any study related assessments or procedures
Understand and voluntarily sign an informed consent form
Patients must be able to understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Fully understand the study and voluntarily sign the informed consent form;
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Able to understand and to provide voluntarily informed consent
Newly diagnosed MCL: Understand and voluntarily sign an IRB-approved informed consent form
Understand and voluntarily sign an informed consent document
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form.
Patients must understand and voluntarily sign an informed consent form
Subject must voluntarily sign and understand written informed consent.
Must understand and voluntarily sign informed consent;
Subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted
Subject must understand and voluntarily sign an informed consent form (ICF) prior to any study-related assessments/procedures being conducted.
Understand and voluntarily sign a biomarker-specific component of the informed consent form prior to any study-related procedures conducted.
Understand and voluntarily sign an ICD (Informed Consent Document) prior to any study related assessments/procedures are conducted.
Understand and voluntarily sign and date an informed consent document prior to any study related assessments/procedures are conducted.
Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures are conducted.
Subjects must voluntarily sign an ICF;
Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures are conducted.
Voluntarily agree to participate and sign an informed consent document
Patient must understand and voluntarily sign an informed consent, and be able to comply with study procedures and follow-up examinations
Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures are conducted.
Participant understands and voluntarily signs an informed consent document prior to any study related assessments or procedures are conducted.
Understand and voluntarily sign an informed consent form
The patient (when applicable) or patient's parent(s) or legal guardian(s) understand(s) and voluntarily signed an informed consent document prior to any study-related assessments/procedures being conducted. Where locally applicable, the patient also understands and voluntarily provides his/her assent prior to any study-related assessments/procedures being conducted.
Understand and voluntarily sign an informed consent form
Must understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form.
Must understand and voluntarily sign an informed consent document.
Understand and voluntarily signed informed consent
Patient must understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Understand and voluntarily sign an informed consent form
Must understand and voluntarily sign an informed consent form.
Subject understands and voluntarily signs an informed consent document prior to conducting any study related assessments/procedures
Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures being conducted.
Patient must understand and voluntarily sign an informed consent form, with the understanding that the patient may withdraw consent at any time without prejudice to future medical care
Understand and voluntarily sign an informed consent form prior to any study related assessments/procedures being conducted.
Understand and voluntarily sign an informed consent form
Understand and voluntarily provide written consent to the Informed Consent Form prior to conducting any study related assessments/procedures.
Patients must be able to understand and voluntarily sign an informed consent form
Willing and able to understand and voluntarily sign a written informed consent
Understand and voluntarily sign informed consent form
Must understand and voluntarily sign informed consent form
Understand and voluntarily sign an informed consent document prior to any study-related assessments or procedures conducted.
Understand and voluntarily sign a biomarker-specific component of the informed consent document prior to any study-related procedures conducted.
Subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted.
Understand and voluntarily sign an informed consent form
Must understand and voluntarily have signed an Informed Consent after its contents have been fully explained.
Voluntarily agree to participate and sign an informed consent document
Patients must be able to read, understand, and voluntarily sign an informed consent document
The subject's parent(s)/legal guardian(s) understand(s) and voluntarily signed an informed consent document prior to any study-related assessments/procedures being conducted. Where locally applicable, the subject also understands and voluntarily provides his/her assent prior to any study-related assessments/procedures being conducted
Must understand and voluntarily sign an informed consent form after the contents have been fully explained to them
Must understand and voluntarily have signed an Informed Consent after its contents have been fully explained
Subject must understand and voluntarily sign an ICD prior to any study-related assessments/procedures being conducted.