Study of Durvalumab and Tremelimumab as First-line Treatment in Patients With Advanced Hepatocellular Carcinoma



Status:Recruiting
Conditions:Liver Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 100
Updated:3/10/2019
Start Date:October 11, 2017
End Date:June 30, 2021
Contact:AstraZeneca Clinical Study Information Center
Email:information.center@astrazeneca.com
Phone:1-877-240-9479

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A Randomized, Open-label, Multi-center Phase III Study of Durvalumab and Tremelimumab as First-line Treatment in Patients With Advanced Hepatocellular Carcinoma

This is a randomized, open-label, multi-center, global, Phase III study to assess the
efficacy and safety of durvalumab plus tremelimumab combination therapy and durvalumab
monotherapy versus sorafenib in the treatment of patients with no prior systemic therapy for
unresectable HCC. The patients cannot be eligible for locoregional therapy.

The study population includes patients 18 years of age or older with advanced HCC, Barcelona
Clinic Liver Cancer stage B not eligible for locoregional therapy or stage C, and Child-Pugh
A classification liver disease. Patients must not have received any prior systemic therapy
for unresectable HCC.

Patients in all treatment arms may continue receiving their originally assigned treatment, at
the Investigator's discretion, until progression

Patients in all arms with confirmed PD who, in the Investigator's opinion, continue to
receive benefit from their assigned treatment and meet the criteria for treatment in the
setting of PD may continue to receive their assigned treatment.

If a patient discontinues study drug(s) due to disease progression, the patient will enter
survival follow-up. Patients who have discontinued treatment due to toxicity or symptomatic
deterioration or who have commenced subsequent anticancer therapy, will have tumor
assessments until confirmed PD and will be followed for survival.

Inclusion criteria

- HCC based on histopathological confirmation

- No prior systemic therapy for HCC

- Barcelona Clinic Liver Cancer (BCLC) stage B (that is not eligible for locoregional
therapy) or stage C

- Child-Pugh Score class A

- ECOG performance status of 0 or 1 at enrollment

Exclusion criteria

- Hepatic encephalopathy within past 12 months or requirement for medication to prevent
or control encephalopathy

- Clinically meaningful ascites

- Main portal vein tumor thrombosis

- Active or prior documented GI bleeding (eg, esophageal varices or ulcer bleeding)
within 12 months

- HBV and HVC co-infection, or HBV and Hep D co-infection
We found this trial at
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Seattle, WA
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Ann Arbor, MI
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Boston, MA
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Charlotte, North Carolina 28207
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Chicago, IL
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Durham, NC
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Fort Myers, FL
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Germantown, TN
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Hartford, CT
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Jacksonville, FL
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New Orleans, LA
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Rochester, MN
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Saint Petersburg, Florida 33713
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Saint Petersburg, FL
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Washington,
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Westwood, KS
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