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Completed Phase 3 Interventional Results available

A Multicenter, Open-Label, Phase 3 Trial to Compare the Efficacy and Safety of Lenvatinib (E7080) Versus Sorafenib in First-line Treatment of Participants With Unresectable Hepatocellular Carcinoma

ClinicalTrials.gov ID: NCT01761266

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT01761266. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 12, 2026, 6:13 PM EST

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Official title

A Multicenter, Randomized, Open-Label, Phase 3 Trial to Compare the Efficacy and Safety of Lenvatinib (E7080) Versus Sorafenib in First-Line Treatment of Subjects With Unresectable Hepatocellular Carcinoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

E7080-G000-304 is a multicenter, randomized, open-label, noninferiority Phase 3 study to compare the efficacy and safety of lenvatinib versus sorafenib as a first-line systemic treatment in participants with unresectable Hepatocellular Carcinoma (HCC).

Study identification

NCT ID
NCT01761266
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eisai Limited
Industry
Enrollment
954 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 1, 2013 (Actual)
Primary completion
Nov 13, 2016 (Actual)
Completion
Mar 10, 2021 (Actual)
Last update posted
Apr 5, 2022

2013 – 2021

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Facility # 1 Los Angeles California — —
Facility # 1 Sacramento California — —
Facility # 1 San Francisco California — —
Facility # 1 Washington D.C. District of Columbia — —
Facility # 1 Tampa Florida — —
Facility # 1 Duluth Georgia — —
Facility # 1 Lawrenceville Georgia — —
Facility # 1 Baltimore Maryland — —
Facility # 1 Detroit Michigan — —
Facility # 1 Kansas City Missouri — —
Facility # 1 St Louis Missouri — —
Facility # 1 East Orange New Jersey — —
Facility # 1 Brooklyn New York — —
Facility # 1 Lake Success New York — —
Facility # 1 New York New York — —
Facility # 1 Charlotte North Carolina — —
Facility # 1 Durham North Carolina — —
Facility # 1 Portland Oregon — —
Facility # 1 Austin Texas — —
Facility # 1 Lubbock Texas — —
Facility # 1 Seattle Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 165 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01761266, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 5, 2022 · Synced Nov 12, 2026

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