drugset / Trial / NCT05147337

A Study to Assess the Safety and Tolerability of E2511 in Healthy Adult and Elderly Participants

NCT05147337 ↗

Phase 1 Completed 47 enrolled Eisai Inc.
RandomizedParallel-groupDouble-blindOther

Summary

The primary objective of this study is to evaluate the safety, tolerability, and plasma pharmacokinetic (PK) of E2511 following multiple oral doses in healthy adult participants.

Timeline

Start
2021-12-01
Primary completion
2022-08-18
Completion
2022-08-18

Drugs

EvaluationDrugModalityDoseRoute
Subject E2511 Unknown 10 mg Oral
Subject E2511 Unknown 20 mg Oral
Subject E2511 Unknown 40 mg Oral
Subject E2511 Unknown 80 mg Oral

Indications

No indication recorded.