Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from giving informed consent.
Any serious medical condition, laboratory abnormality, or psychiatric illness that would – in the opinion of the investigator – prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from giving informed consent.
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent.
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent document or complying with the protocol treatment
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from providing informed consent
Medical, psychiatric or other condition that would prevent the patient from receiving the protocol therapy or providing informed consent
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious psychological condition or psychiatric illness that would prevent the subject from signing the informed consent document, in the investigator opinion
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent document or complying with the protocol treatment
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
Patients who have any serious condition, laboratory abnormality, or psychiatric illness that would prevent them from singing the informed consent form are NOT eligible for participation
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from providing informed consent
Patients must not have any serious medical condition or any other unstable medical co-morbidity, or psychiatric illness that will prevent the subject from signing the informed consent form or will place the subject at unacceptable risk if he/she participates in the study
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition or psychiatric illness that would prevent the patient from providing informed consent
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent document.
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, uncontrolled intercurrent illness, or psychiatric illness/social condition that would prevent the participant from signing the informed consent form
Any serious medical condition, laboratory abnormality, uncontrolled intercurrent illness, or psychiatric illness/social condition that would prevent the participant from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality or psychiatric illness that would prevent obtaining informed consent
Any serious medical condition or psychiatric illness that will prevent the subject from signing the informed consent form or will place the subject at unacceptable risk if he/she participates in the study
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality or psychiatric illness that would prevent obtaining informed consent
Any serious medical condition laboratory abnormality or psychiatric illness that would prevent the subject from signing the consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
Patient has any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent him/her from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any medical condition, that would prevent the subject from signing the informed consent form.
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent subject from providing informed consent
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition or psychiatric illness that would prevent the patient from providing informed consent
Any serious medical condition or psychiatric illness that would prevent the subject from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subjects from signing the informed consent form
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing informed consent form
Any serious medical condition or psychiatric illness that would prevent the patient from providing informed consent
Any serious medical condition laboratory abnormality or psychiatric illness that would prevent the subject from signing the consent form
Any serious medical condition, laboratory abnormality, uncontrolled intercurrent illness, or psychiatric illness/social condition that would prevent the participant from signing the informed consent form
Patients with mental deficits or psychiatric conditions that preclude them from giving informed consent or following protocol
Psychiatric illness, which would prevent the patient from giving informed consent or adhering to the study protocol.
Patients have voluntarily agreed to participate by giving written informed consent.
Patients who have any debilitating medical or psychiatric illness that would preclude their giving informed consent or their receiving optimal treatment and follow up
Subjects must be willing to sign and provide informed consent and be capable of giving informed consent in accordance with the Institutional Review Board/Ethics Committee policy
A patient must be capable of giving informed consent or have an acceptable surrogate capable of giving consent on the subject’s behalf
Any mental or medical condition that prevents the subject from giving informed consent or participating in the trial.
Patients with mental deficits and/or psychiatric history that preclude them from giving informed consent or from following protocol
Must be capable of giving consent to participate in the study
Has any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
Patients must be capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Patients must be capable of giving informed consent and be willing and able to comply with schedule
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form
Patient, or patient's authorized representative, must be willing and capable of giving written Informed Consent and must be able to adhere to dosing and visit schedules as well as meet all study requirements
Capable of giving written informed consent prior to any study-specific procedures
Capable of giving signed informed consent
Psychiatric illness, which would prevent the patient from giving informed consent
Has any mental or medical condition that prevents the patient from giving informed consent
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form
Patient has voluntarily agreed to participate by giving written informed consent/assent for the trial
Patient capable of giving informed consent
Patient capable of giving informed consent
Patient has voluntarily agreed to participate by giving written informed consent
All patients must be consented prior to chemotherapy; the patient should not have any serious medical or psychiatric illness that would prevent either the giving of informed consent or the receipt of treatment
Patients who have any debilitating medical or psychiatric illness that would preclude their giving informed consent or their receiving optimal treatment and follow-up
Patients who have any debilitating medical or psychiatric illness that would preclude their giving informed consent or their receiving optimal treatment and follow-up
Capable of giving signed informed consent which includes compliance with the requirements and restrictions specified. Additional Inclusion criteria for Subjects in Part 2:
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form
Subjects who have voluntarily agreed to participate by giving written informed consent.
Adults capable of giving informed consent.
Capable of giving signed informed consent.
Patient is capable of giving informed consent
Capable of giving written informed consent
Able to give informed consent (if > 18 years), or with a legal guardian capable of giving informed consent (if < 18 years)
DONOR: Donors able to give informed consent (if > 18 years), or with a legal guardian capable of giving informed consent (if < 18 years)
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form. If the subject is less than 18 years old, an Assent form and parental/guardian Consent form (replacing \you will\ with \your child will\ will be required).
Matched Related Donor: Capable of giving written, informed consent
Subject has voluntarily agreed to participate by giving written informed consent
No debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment and follow-up
Capable of giving informed consent
Capable of giving written informed consent, which includes compliance with the requirements and restrictions
Has any mental or medical condition that prevents the subject from giving informed consent or participating in the trial
Any mental or medical condition that prevents the subject from giving informed consent or participating in the trial.
Patient has a debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment or follow up.
Any serious medical or psychiatric illness that would prevent either the giving of informed consent or the receipt of treatment
Patient must be capable of, and must voluntarily agree to participate by giving written informed consent
Patients may not have any debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment and follow-up
Patient is capable of giving informed consent.
The patient or their legally acceptable representative must be capable of giving written informed consent prior to performing any study-specific tests or procedures.
Adult patients who are capable of giving consent
Capable of giving signed, written informed consent
Capable of giving informed consent
Subjects must be capable of giving informed consent
Capable of giving informed consent
Subjects are capable of giving informed consent or have an acceptable surrogate capable of giving consent on the subject’s behalf
Not giving consent for study participation
Subjects are capable of giving informed consent
Women with psychological, psychiatric, or other conditions which prevent giving fully informed consent
Subjects are capable of giving informed consent.
Incapable of giving informed consent
Psychiatric illness that would prevent the patient from giving informed consent
No debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment and follow-up
Capable of giving informed consent
Subjects capable of giving informed consent
Subject capable of giving informed consent and participating in the process of consent
Subject capable of giving informed consent and participating in the process of consent
Individuals who are not willing or capable of giving informed consent or assent (with legal guardian consent)
Subjects incapable of giving informed written consent
Patients are capable of giving informed consent
Patients are capable of giving informed consent
Other severe acute or chronic medical or psychiatric condition or laboratory abnormality
Has a serious illness or medical condition(s)
Any known clinically significant concomitant medical condition, laboratory abnormality, or psychiatric illness that, in the investigator’s opinion, would prevent the subject from participating in the study, pose an unacceptable risk to the patient in this study, or interfere with the interpretation of safety results
Any other significant medical illness, abnormality, or condition
Serious illness or medical condition.
Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any serious medical condition, laboratory abnormality, uncontrolled intercurrent illness, or psychiatric illness/social condition that would prevent study participation
Any serious medical condition, laboratory abnormality, uncontrolled intercurrent illness, or psychiatric illness/social condition that would prevent study participation
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from participating in the study
Patients with any concurrent uncontrolled clinically significant medical condition, including infection, laboratory abnormality, or psychiatric illness which could place the patient at unacceptable risk of study treatment.
Patients who have prior or ongoing clinically significant illness, medical condition, surgical history, physical finding, or laboratory abnormality as determined by the investigator.
Subject who, in the opinion of the Investigator, has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
A serious illness or medical condition
Serious illness or medical condition that could affect the safety or tolerability of study treatments
Subject has concurrent, uncontrolled medical condition, laboratory abnormality, or psychiatric illness, which could place him/her at unacceptable risk
Has a serious illness or medical condition(s) that would affect safety or tolerability of the study treatments
Other serious illness or medical condition(s) (see protocol)
Unstable or severe uncontrolled medical condition (eg, unstable cardiac function, unstable pulmonary condition), or any important medical illness or abnormal laboratory finding that would, in the Investigator's judgment, increase the subject's risk while participating in this study
Any other significant medical condition, including psychiatric illness or laboratory abnormality, that would preclude the patient participating in the trial or would confound the interpretation of the results of the trial
Any serious medical condition or abnormality in clinical laboratory tests
Any significant medical condition, laboratory abnormality, or psychiatric illness, that would prevent subjects from participating in the study, including the inability to swallow capsules
The participant has a serious illness or medical condition including:
Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any other significant medical illness, abnormality, or condition.
Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study
Any significant medical condition, laboratory abnormality, or psychiatric illness
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Serious concurrent illness, altered medical status or any uncontrolled medical condition
Other serious concurrent illness or medical condition.
Unstable or severe uncontrolled medical condition (eg, unstable cardiac function, unstable pulmonary condition), or any important medical illness or abnormal laboratory finding that would, in the investigator's judgment, increase the subject's risk while participating in this study
The patient has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from participating in the study.
Any important medical illness or abnormal laboratory finding that would increase the risk of participating in this study
Certain serious illness or medical condition(s)
For Part D, have a serious illness or medical condition(s), including but not limited to the following:
Any concurrent, uncontrolled medical condition, laboratory abnormality, or psychiatric illness which could place him/her at unacceptable risk
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Known serious illness or medical condition
Other serious concurrent illness or medical condition.
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Prior or ongoing clinically significant illness, medical condition, surgical history, physical finding, electrocardiogram (ECG) finding, or laboratory abnormality
Any serious illness or medical condition that could affect participation on trial
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
Any important medical illness or abnormal laboratory finding that would increase the risk of participating in this study
Serious cardiac illness or medical condition including but not confined to:
Clinically significant illness, medical condition, surgical history, physical finding, or laboratory abnormality that could affect the safety of the patient; alter the absorption of the study drugs; or impair the assessment of study results.
Other serious concurrent illness or medical condition.
Any serious medical condition, laboratory abnormality, or psychiatric illness that, in the view of the treating physician, would place the participant at an unacceptable risk if he or she were to participate in the study or would prevent that person from giving informed consent.
Any serious medical condition, lab abnormality or psychiatric illness
Any important medical illness or abnormal laboratory finding that would, in the investigator's judgment, significantly increase the subject's risk of participating in this study
Any serious medical condition, laboratory abnormality, or psychiatric illness that, in the view of the treating physician, would place the participant at an unacceptable risk if he or she were to participate in the study or would prevent that person from giving informed consent
Any significant medical condition, laboratory abnormality, or psychiatric illness that, as determined by the treating Investigator, would prevent the subject from participating in the study or providing written informed consent
Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study
Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study based on investigator´s judgment.
Has a serious illness or medical condition(s)
Chronic gastrointestinal illness
Uncontrolled serious medical or psychiatric illness
Patients with an active psychiatric or mental illness making informed consent or careful clinical follow-up unlikely are excluded
Patients should have NO significant medical or psychiatric illness that would interfere with compliance and ability to tolerate treatment as outlined in the protocol
Severe psychiatric illness or mental deficiency making compliance to treatment unlikely and/or informed consent impossible
DONOR: Severe psychiatric illness or mental deficiency making compliance with donation unlikely and/or informed consent impossible
Mental incapacitation or psychiatric illness that would preclude study participation
A major psychiatric illness which would limit understanding of the proposed protocol treatment and consent process
Patients with severe co-extensive comorbidities or significant psychiatric illness
Any serious medical illness, other than that treated by this study, which would limit survival to less than 1 month or psychiatric illness which would limit informed consent
Patients with a history of serious co-morbid illness or uncontrolled illnesses that would preclude protocol therapy.
Any serious medical illness, other than treated by this study, which would limit survival to less than 1 month or psychiatric illness which would limit informed consent
Patients with a mental disorder, psychiatric illness/social or concussion which would inhibit their ability to provide informed consent or prevent compliance with follow-up
Patients should not have a history of significant psychiatric illness
If history of depression or psychiatric illness, has to be well controlled with antidepressants and/or under psychiatrist/ psychologist care
Severe psychiatric illness or mental deficiency sufficiently severe as to make compliance with the transplant treatment unlikely and informed consent impossible
Significant underlying medical or psychiatric illness
Have additional uncontrolled serious medical or psychiatric illness.
Other serious medical illness other than that treated by this study which would limit survival to <2 years or psychiatric conditions which would prevent informed consent or compliance with treatment.
Patients with serious unstable medical illness
Patients must not have a serious medical or psychiatric illness which prevents informed consent or compliance with treatment
Psychiatric illness which may make compliance to the clinical protocol unmanageable or which may compromise the ability of the patient to give informed consent
Patients with serious unstable medical illness
Significant underlying medical or psychiatric illness.
Patients should not have a history of significant psychiatric illness
Significant underlying medical or psychiatric illness
Significant underlying medical or psychiatric illness
Psychiatric illness that may affect the patient's compliance with the treatment.
Subjects with uncontrolled medical or mental illness that, in the Investigator's judgement, could affect treatment tolerability or compliance.
Have psychiatric or other medical illness, or any other condition that in the opinion of the investigator prevents compliance with the study procedures or ability to provide valid informed consent.
Psychiatric, other medical illness or other condition that in the opinion of the principal investigator (PI) prevents compliance with study procedures or ability to provide valid informed consent.
No serious medical or psychiatric illness which prevents informed consent or intensive treatment is allowed
Medical or psychiatric illness which would compromise the patient's ability to tolerate treatment or limit compliance with study requirements
Patients with serious unstable medical illness
Psychiatric, other medical illness or other condition that in the opinion of the PI prevents compliance with study procedures or ability to provide valid informed consent
Psychiatric, other medical illness or other condition that in the opinion of the PI prevents compliance with study procedures or ability to provide valid informed consent.
Psychiatric, other medical illness or other condition that in the opinion of the PI prevents compliance with study procedures or ability to provide valid informed consent
uncontrolled psychiatric illness;
Significant psychiatric illness
If the patient has co-morbid medical illness, life expectancy attributed to the comorbid illness must be greater than 6 months
Significant or acute medical illness
Evidence of significant medical illness, abnormal laboratory finding or psychiatric illness/social situations that would, in the investigator’s judgment, makes the patient inappropriate for this study
Other uncontrolled, concurrent illness that would preclude study participation; or, psychiatric illness or social challenges that would entail unreasonable risk or preclude informed consent or compliance with study procedures
Subjects who have a history of significant psychiatric illness
Have no active cardiac, neurologic, or psychiatric illness, and
No significant co-morbid medical or psychiatric illness that would significantly compromise the patient’s clinical care and chances of survival
Patients must not have a severe psychiatric illness, including major depression or any previous suicide attempts
Hospitalized for psychiatric illness within the past two years
Patient has a serious medical or psychiatric illness which prevents informed consent or adherence with treatment
Psychiatric illness that may make compliance to the clinical protocol unmanageable or may compromise the ability of the patient to give informed consent
Severe concomitant medical or psychiatric illness
Any debilitating medical or psychiatric illness that would preclude ability to give informed consent or receive optimal treatment and follow-up
DONOR: Untreatable/unstable psychiatric illness
Patients with serious unstable medical illness
No serious medical or psychiatric illness which prevents informed consent or intensive treatment
Serious intercurrent medical or psychiatric illness
Patients with serious unstable medical illness
Patients should have no significant psychiatric illness or medical illness that would preclude the ability to comply with the protocol
Concurrent serious medical illness that could potentially interfere with protocol compliance (such medical illness will not include hepatitis or cirrhosis, as the degree of liver impairment caused by these diseases are covered by other exclusion criteria).
Patients should have no significant psychiatric illness or medical illness that would preclude the ability to comply with the protocol
Any serious medical or psychiatric illness
Comorbid systemic illness or psychiatric illness that could interfere with study completion
Any serious medical or psychiatric illness
History of clinically significant psychiatric illness that would prevent the patient from providing a valid ICF and complying with protocol requirements
Have additional uncontrolled serious medical or psychiatric illness.
Severe concomitant medical or psychiatric illness
Must be cognitively intact and free of serious psychiatric illness (as determined by study recruiter at intake)
Significant psychiatric disturbance verified by medical record sufficient to preclude completion of the assessment measures, interview or informed consent (i.e. acute psychiatric symptoms which require individual treatment)
Major psychiatric illness or comorbid conditions prohibiting compliance with study procedures as determined by the treating oncologist
Diagnosis of major mental illness on the medical record (verified by the recruiter)
Patients with any medical illness or concurrent psychiatric illness which, in the investigators’ opinion, cannot be adequately controlled with appropriate therapy
Immunosuppression as a result of underlying illness or treatment;
Major psychiatric illness or co-morbid conditions prohibiting compliance with study procedures
History of hospitalization for psychiatric illness
Have a diagnosis of psychiatric illness or other major illness in addition to PCa, such as other cancers, uncontrolled hypertension, lung disease, liver disease or heart disease
Serious underlying medical comorbidity such as uncontrolled hypertension, cardiovascular disease, pulmonary disease, psychiatric illness, or any other condition for which the patient is not approved for exercise by their physician
Self-report of hospitalization for psychiatric illness within the last two years
Unstable self-reported medical or psychiatric illness (Axis I – current or within the last 5 years) that would make it unsafe or impossible to adhere to the study protocol
No history of prior inpatient psychiatric treatment for severe mental illness within 1 year (e.g., psychosis)
History of prior inpatient psychiatric treatment for severe mental illness within the past year (e.g., psychosis),
DONOR: Severe psychiatric illness. Mental deficiency sufficiently severe as to make compliance with the donation procedure unlikely, and making informed consent impossible
Participants who exhibit confusion, disorientation, or have a history of major psychiatric illness which may impair their understanding of the informed consent
Severe psychiatric illness
Severe psychiatric illness
No uncontrolled serious medical or psychiatric illness
Have been hospitalized for treatment of a major psychiatric illness within the last five years
Poorly controlled hypertension, DM or other serious medical/psychiatric illness