Last reviewed · How we verify

NCT04683185

A Study to Assess the Safety and Tolerability of E6742 in Japanese Healthy Adult Participants

Completed Phase 1 Last updated 20 July 2021
What this trial tests

Phase 1 trial testing E6742 in Healthy Volunteers in 24 participants. Completed in 21 June 2021.

Timeline
28 December 2020
Primary endpoint
21 June 2021
21 June 2021

Quick facts

Lead sponsorEisai Co., Ltd.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeother
Enrollment24
Start date28 December 2020
Primary completion21 June 2021
Estimated completion21 June 2021
Sites1 location across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Eisai Co., Ltd. — full company profile →

Who can join

Adults 20 to 55, any sex, with Healthy Volunteers. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary purpose of the study is to evaluate the safety, tolerability and pharmacokinetics (PK) of multiple ascending oral doses of E6742 in Japanese healthy adult participants.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A new therapeutic target for systemic lupus erythematosus: the current landscape for drug development of a toll-like receptor 7/8 antagonist through academia-industry-government collaboration.
    Tanaka Y, Tago F, Yamakawa N, Aoki M, et al · · 2024 · cited 8× · PMID 37772762 · DOI 10.1080/25785826.2023.2264023

Verify or expand the search:

Other trials of E6742

Trials testing the same drug.

Other recruiting trials for Healthy Volunteers

Currently open trials in the same condition.

Other Eisai Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04683185.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing