drugset / Trial / NCT03433703

Trial to Evaluate Safety and Efficacy of Treatment of Physician Choice (TPC) Following First-Line Treatment of Lenvatinib in Subjects With Unresectable Hepatocellular Carcinoma (uHCC)

NCT03433703 ↗

Phase 2 Terminated 8 enrolled Eisai Inc.
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to assess the safety and tolerability of subsequent systemic treatment of physician's choice (TPC) following the first-line lenvatinib treatment in unresectable hepatocellular carcinoma (uHCC) participants.

Timeline

Start
2018-04-26
Primary completion
2019-01-07
Completion
2019-01-07

Outcome

Outcome not reported

Stopped (Enrollment): “Study recruitment was stopped due to difficulty in enrolling the targeted number of participants.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenvatinib Small molecule 8 mg Oral
Subject Lenvatinib Small molecule 12 mg Oral