--- a
+++ b/clusters/9knumclustersv2/clust_1333.txt
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+Participants must, in the opinion of the investigator, be capable of complying with the protocol
+The subject is capable of understanding and complying with protocol requirements.
+Participants must in the opinion of the investigator be capable of complying with this protocol
+Patients in whom there is a medical contraindication or potential problem in complying with the requirements of the protocol, in the opinion of the investigator.
+Capable of understanding and complying with protocol requirements.
+Participants must, in the opinion of the Investigator, be capable of complying with the requirements of this protocol including self-administration of study treatment
+mCRPC EXPANSION COHORT: Patient must be capable of understanding and complying with protocol requirements and is willing to give informed consent
+Participants in whom there is a medical contraindication or potential problem in complying with the requirements of the protocol, in the opinion of the investigator
+Patient must be capable of understanding and complying with protocol requirements and is willing to give informed consent
+The subject is capable of understanding and complying with parameters as outlined in the protocol
+Patient must be capable of understanding and complying with protocol requirements and is willing to give informed consent
+The subject is capable of understanding and complying with parameters as outlined in the protocol
+In the opinion of the investigator, the participant or legal guardian is capable of understanding and complying with protocol requirements for the duration of the study.
+Psychiatric disorders or other conditions rendering the subject incapable of complying with the requirements of the protocol
+Participants must, in the opinion of the investigator, be capable of complying with the protocol
+Must in the opinion of the investigator be capable of complying with this protocol
+Participants must, in the opinion of the investigator, be capable of complying with the protocol
+Written voluntary informed consent: the patient is capable of complying with the requirements of the written Informed Consent Form and complying with protocol requirements
+Subjects must in the opinion of the Investigator be capable of complying with this protocol
+Participants must be capable of understanding and complying with the protocol requirements and signing informed consent
+Participants must, in the opinion of the investigator, be capable of complying with the requirements of this protocol
+Capable of complying with study procedures and communicating with study personnel
+Patient is capable of complying with study procedures
+Patient is capable of complying with study procedures
+Patient is capable of complying with study procedures
+Patient is capable of complying with study procedures
+Capable of understanding and complying with protocol requirements.