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NCT02269995

Post-marketing Surveillance of DC Bead in Patients With Hepatocellular Carcinoma

Completed Last updated 5 November 2018
What this trial tests

trial testing E7040 in Hepatocellular Carcinoma in 300 participants. Completed in 25 December 2015.

Timeline
6 March 2014
Primary endpoint
14 May 2015
25 December 2015

Quick facts

Lead sponsorEisai Co., Ltd.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment300
Start date6 March 2014
Primary completion14 May 2015
Estimated completion25 December 2015
Sites1 location across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Eisai Co., Ltd. — full company profile →

Who can join

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

Sponsor's own description

This surveillance's objectives are: 1. Unknown adverse reactions 2. Incidences of adverse drug reaction 3. Factors considered to have effect to safety and effectiveness

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 recruiting trials for Hepatocellular Carcinoma

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/NCT02269995.

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