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)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lenvatinib | Small molecule | 8 mg | Oral |
| Subject | Lenvatinib | Small molecule | 12 mg | Oral |