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Clinical Trial Summary

The primary purpose of the study is to investigate the incidence of adverse drug reactions (ADRs) (ADR of special interest: capillary leak syndrome, infusion reaction, rhabdomyolysis, myelosuppression, infection, hepatic dysfunction, visual impairment/color blindness, ischemic heart disease/arrhythmia/cardiac failure, and severe skin disorders).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05137847
Study type Observational
Source Eisai Inc.
Contact
Status Completed
Phase
Start date May 24, 2021
Completion date March 17, 2023

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