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.