malignant tumors
Conditions
Interventions
None listed
Sponsors
National Cancer Center Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Subjects enrolled or be considered for enrollment in early clinical trials.
Exclusion criteria
Exclusion criteria: Subjects reject exploratory analyses using clinical specimens.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To investigate the efficacy and validity of identifying optimal population and biomarkers that predict the occurrence of adverse events in early clinical trials according to the results of the comprehensive analysis of genetic analyses and immunological profiling | — |
Countries
Japan
Contacts
Public ContactJun Sato
National Cancer Center Hospital Department of Experimental Therapeutics
Outcome results
None listed