Eisai Clinical Trials
Study Overview
E2086
N/A
NCT06481488
Jun 2024 - Dec 2024
Healthy Volunteers
1. Part A: Number of Participants With Treatment-emergent Adverse Events (TEAEs) [Time Frame: Day 10]
2. Part A: Number of Participants With Serious Adverse Events (SAEs) [Time Frame: Day 10]
3. Part A: Number of Participants With Clinically Significant Abnormal Laboratory Parameters [Time Frame: Day 10]
4. Part A: Number of Participants With Clinically Significant Abnormal Vital Signs Values [Time Frame: Day 10]
2. Part A: Number of Participants With Serious Adverse Events (SAEs) [Time Frame: Day 10]
3. Part A: Number of Participants With Clinically Significant Abnormal Laboratory Parameters [Time Frame: Day 10]
4. Part A: Number of Participants With Clinically Significant Abnormal Vital Signs Values [Time Frame: Day 10]
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Males and females 18 Years to 55 Years (Adult)
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Completed -
Phase 1
United StatesData Sharing
ClinicalStudyDataRequest.com (CSDR) is a multi sponsor site through which qualified researchers who wish to access clinical trial data and associated information in order to conduct further research can submit their research proposal or enquiry.
CSDR Sharing is not available for this study.
CSDR Availability Clinical Trial Data Redacted documents may be available upon request for this study.
Document type Availability Protocol SAP Sample CRF Full CSR