A Study to Assess the Safety and Efficacy of Lenvatinib as First-line Treatment in Participants With Unresectable HCC

NCT04297254 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2023-11-15

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the safety of lenvatinib in HCC.

Conditions

  • Carcinoma, Hepatocellular

Interventions

DRUG

Lenvatinib

Lenvatinib capsules.

Sponsors & Collaborators

  • Eisai Pharmaceuticals India Pvt. Ltd

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-04
Primary Completion
2023-07-31
Completion
2023-07-31

Countries

  • India

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04297254 on ClinicalTrials.gov