ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

A Global Study to Evaluate Transarterial Chemoembolization (TACE) in Combination With Durvalumab and Bevacizumab Therapy in Patients With Locoregional Hepatocellular Carcinoma

ClinicalTrials.gov ID: NCT03778957

Public ClinicalTrials.gov record NCT03778957. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 21, 2026, 12:56 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III, Randomized, Double-blind, Placebo-controlled, Multicenter Study of Transarterial Chemoembolization (TACE) in Combination With Either Durvalumab Monotherapy or Durvalumab Plus Bevacizumab Therapy in Patients With Locoregional Hepatocellular Carcinoma (EMERALD-1)

Study identification

NCT ID
NCT03778957
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
724 participants

Conditions and interventions

Interventions

  • Bevacizumab Drug
  • Durvalumab Drug
  • Placebo Other
  • Transarterial Chemoembolization (TACE) Procedure

Drug · Other · Procedure

Eligibility (public fields only)

Age range
18 Years to 110 Years
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
Nov 29, 2018
Primary completion
Sep 10, 2023
Completion
Aug 30, 2026
Last update posted
Apr 14, 2026

2018 – 2026

United States locations

U.S. sites
24
U.S. states
18
U.S. cities
22
Facility City State ZIP Site status
Research Site Costa Mesa California 92627
Research Site La Jolla California 92093-0698
Research Site Orange California 92868
Research Site Washington D.C. District of Columbia 20007
Research Site Jacksonville Florida 32224
Research Site Miami Florida 33136
Research Site Honolulu Hawaii 96819
Research Site Chicago Illinois 60612
Research Site Shreveport Louisiana 71103
Research Site Detroit Michigan 48201
Research Site Rochester Minnesota 55905-0001
Research Site St Louis Missouri 63110
Research Site Stony Brook New York 11794
Research Site Charlotte North Carolina 28204
Research Site Cleveland Ohio 44106
Research Site Portland Oregon 97213
Research Site Pittsburgh Pennsylvania 15212
Research Site Sioux Falls South Dakota 57105
Research Site Memphis Tennessee 38104
Research Site Dallas Texas 75216
Research Site Dallas Texas 75235
Research Site Houston Texas 77030
Research Site Houston Texas 77090
Research Site Milwaukee Wisconsin 53226

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 142 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03778957, 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 14, 2026 · Synced May 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03778957 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →