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NCT03663114

A Post-marketing Observational Study on Risk Factors for Hepatic Encephalopathy in Participants With Unresectable Hepatocellular Carcinoma

Completed Last updated 22 January 2021
What this trial tests

trial testing Lenvatinib in Carcinoma, Hepatocellular in 713 participants. Completed in 20 February 2020.

Timeline
2 July 2018
Primary endpoint
20 February 2020
20 February 2020

Quick facts

Lead sponsorEisai Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment713
Start date2 July 2018
Primary completion20 February 2020
Estimated completion20 February 2020
Sites2 locations across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Eisai Inc. — full company profile →

Who can join

18 and older, any sex, with Carcinoma, Hepatocellular. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a post-marketing observational study of lenvatinib in participants with unresectable hepatocellular carcinoma. The primary objective of this study is assessment of risk factors for hepatic encephalopathy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Lenvatinib

Trials testing the same drug.

Other recruiting trials for Carcinoma, Hepatocellular

Currently open trials in the same condition.

Other Eisai Inc. 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/NCT03663114.

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