Ability to comply with the study protocol, in the investigator's judgment
Ability and willingness to comply with the study protocol for the duration of the study and with follow-up procedures.
Ability and willingness to comply with the requirements of the study protocol
Patient must have the ability to comply with all study requirements
Ability to comply with study procedures in the Investigator's opinion
Ability to comply with the study protocol, in the investigator's judgment
Willingness and ability to comply with study and follow-up procedures.
Willingness and ability to comply with study and follow-up procedures
Ability to comply with the study protocol, in the investigator's judgment
Limitation of the patient's ability to comply with the treatment or follow-up protocol.
Ability to comply with the protocol
Willingness and ability to comply with protocol-specified Pneumocystis jirovecii pneumonia (PJP) prophylaxis
Willingness and ability to understand the nature of this study and to comply with the study and follow-up procedures.
Willingness and capability to comply with the requirements of the study.
Ability and willingness to comply with the requirements of the study protocol
Willingness and ability to comply with study procedures and follow-up examination
Willingness and ability of the subject to comply with study activities.
Ability to comply with treatment, PK and test schedules
STUDY ENTRY: Ability and willingness to comply with the requirements of the study protocol.
Ability to comply with the study protocol, in the investigator's judgment
Willingness and ability to comply with the trial and follow-up procedures.
Ability to comply with all study procedures and willingness to remain supine for 120 minutes during imaging
Ability to comply with the protocol
Stated willingness to comply with study procedures and duration.
Ability to comply with the protocol
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with the requirements of the study protocol
Ability to comply with the protocol
Stated willingness to comply with all study procedures and be available for the duration of the trial
Ability to comply with protocol requirements.
Ability to comply with the protocol.
Ability and willingness to comply with the requirements of the study protocol
Willingness and ability of subject to comply to study requirements
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with the requirements of the study protocol
Ability to give informed consent and comply with the protocol
Patients must sign informed consent form (ICF) and show ability and willingness to comply with the requirements of the study protocol
Willingness and ability to comply with all study procedures and able to take oral medications
Willingness and ability to comply with study procedures and follow-up examinations
Ability to comply with the protocol
In the investigator’s opinion, the patient has the ability to communicate satisfactorily with the investigator, to participate fully in the study, and comply with all its requirements
Ability to comply with requirements of the protocol, as assessed by the investigator by the patient signing the consent form
Ability to swallow study drugs and to comply with study requirements throughout the study
Willingness to comply with study guidelines
Ability to comply with the protocol procedures (including geographic accessibility)
Have the ability to understand and comply with the requirements and follow-up time points of the study
Willingness and ability to comply with study and follow-up procedures
Willingness and ability to comply with study and follow-up procedures.
Ability and willingness to comply with the requirements of the study protocol.
Ability to give informed consent and comply with the protocol
Ability and willingness to comply with the requirements of the study protocol
Have the willingness and ability to understand the nature of this study and to comply with the study and follow-up procedures.
State willingness to comply with all study procedures and be available for the duration of the trial
Ability and willingness to comply with the requirements of the study protocol
Ability to give written informed consent and willingness to comply with the requirements of the protocol
Ability and willingness to comply with all study requirements
Limitation of the patient's ability to comply with the treatment or to follow-up the protocol.
Have the willingness and ability to comply with scheduled visit and study procedures.
Ability to comply with the study protocol, in the investigator’s judgment
Limitation of the patient's ability to comply with the treatment or follow-up requirements.
Ability and willingness to provide written informed consent, and to comply with the requirements of the protocol
Ability to comply with endometrial biopsies every 3 months
Ability to comply with study procedures
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with the requirements of the study protocol
Willingness and ability to comply with study and follow-up procedures.
Ability and willingness to comply with the requirements of the study protocol
Ability to give written informed consent and willingness to comply with the requirements of the protocol
Ability to give written informed consent and willingness to comply with the requirements of the protocol
Ability to comply with study procedures, in the Investigator's opinion
Ability and willingness to comply with the requirements of the study protocol
Stated willingness of patient to comply with study procedures and reporting requirements.
Ability to comply with endometrial biopsies every 3 months
Ability and willingness to comply with the requirements of the study protocol
Ability to swallow study drugs and to comply with study requirements throughout the study.
Willingness and ability to comply with study and followup procedures.
Willingness and ability to comply with study and follow-up procedures
Ability to comply with an oral drug regimen
Any condition that would interfere with the ability to give informed consent or comply with the study protocol
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with study visits, treatment, testing, and to comply with the protocol, in the investigator's judgment
Willingness and ability to provide written informed consent and to comply with the protocol requirements
Ability to comply with the protocol
Willingness and ability to comply with all study procedures
Written informed consent (and assent when applicable) obtained from subject and ability for subject to comply with the requirements of the study, including the ability to read and speak English.
Any condition that, in the opinion of the enrolling investigator, would interfere with the subject’s ability to comply with the study requirements
Ability to understand and comply with the requirements of this study
Ability to understand and comply with study guidelines
Willingness to comply with study guidelines
Willingness to comply with all study interventions and follow-up procedures including the ability to apply the study drug to the breast
Ability to comprehend and comply with the requirements of the Study
Willingness to comply with all study interventions and follow-up procedures including the ability to swallow the study drug
Willingness to comply with study guidelines
Has any condition that interferes with the ability of the subject to understand or comply with the requirements of the study.
Willingness to comply with the study protocol
Ability to provide signed informed consent and willingness to comply with protocol requirements
Ability and willingness to comply with the study procedures
Willingness to comply with the requirements of the study
Limitation of the patient's ability to comply with the treatment or follow-up protocol.
Willingness and ability to comply with the trial and follow-up procedures.
Willingness and ability to comply with study procedures