Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT05557838

Study of Durvalumab Plus Tremelimumab as First-line Treatment in Chinese Patients With Unresectable Hepatocellular Carinoma

Led by AstraZeneca · Updated on 2025-02-07

210

Participants Needed

32

Research Sites

109 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a prospective, open label, multi-center, interventional study to assess the safety and efficacy of Druvalumab plus Tremelimumab as first-line treatment in Chinese patients with unresectable hepatocellular carcinoma.

CONDITIONS

Official Title

Study of Durvalumab Plus Tremelimumab as First-line Treatment in Chinese Patients With Unresectable Hepatocellular Carinoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed hepatocellular carcinoma by tissue pathology or imaging
  • No previous systemic therapy for hepatocellular carcinoma
  • Barcelona Clinic Liver Cancer (BCLC) stage B not eligible for local therapy, or stage C
  • Child-Pugh liver function class A or B
  • ECOG performance status 0 to 2 at enrollment (class A and ECOG 0-1 in cohort 1, class B or ECOG 2 in cohort 2)
  • At least one measurable tumor lesion according to RECIST 1.1 guidelines
Not Eligible

You will not qualify if you...

  • History of hepatic encephalopathy within past 12 months or needing medication for it
  • Clinically significant ascites (fluid buildup in the abdomen)
  • Main portal vein tumor thrombosis
  • Active or recent gastrointestinal bleeding within past 6 months
  • Co-infection with HBV and HCV or HBV and Hepatitis D

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 32 locations

1

Research Site

Beijing, China, 100021

Active, Not Recruiting

2

Research Site

Beijing, China, 100142

Active, Not Recruiting

3

Research Site

Beijing, China, 211405

Active, Not Recruiting

4

Research Site

Beijing, China, CN-100730

Active, Not Recruiting

5

Research Site

Changsha, China, 410005

Completed

6

Research Site

Changsha, China, 410013

Active, Not Recruiting

7

Research Site

Chengdu, China, 610041

Active, Not Recruiting

8

Research Site

Fuzhou, China, 350011

Active, Not Recruiting

9

Research Site

Guangzhou, China, 510060

Active, Not Recruiting

10

Research Site

Guangzhou, China, 510100

Active, Not Recruiting

11

Research Site

Guangzhou, China, 510260

Active, Not Recruiting

12

Research Site

Guangzhou, China, 510515

Active, Not Recruiting

13

Research Site

Hangzhou, China, 310022

Active, Not Recruiting

14

Research Site

Harbin, China, 150081

Active, Not Recruiting

15

Research Site

Jinan, China, 2501117

Actively Recruiting

16

Research Site

Nanjing, China, 2100008

Active, Not Recruiting

17

Research Site

Nanjing, China, 210009

Active, Not Recruiting

18

Research Site

Nanjing, China, 210029

Active, Not Recruiting

19

Research Site

Ningbo, China, 315010

Active, Not Recruiting

20

Research Site

Shanghai, China, 200032

Active, Not Recruiting

21

Research Site

Shanghai, China, 200040

Active, Not Recruiting

22

Research Site

Shenyang, China, 110001

Active, Not Recruiting

23

Research Site

Tianjin, China, 300000

Active, Not Recruiting

24

Research Site

Tianjin, China, 300060

Withdrawn

25

Research Site

Tianjin, China, 300170

Withdrawn

26

Research Site

Wenzhou, China, 325000

Active, Not Recruiting

27

Research Site

Wuhan, China, 430022

Active, Not Recruiting

28

Research Site

Wuhan, China, 430079

Active, Not Recruiting

29

Research Site

Xi'an, China, 710038

Active, Not Recruiting

30

Research Site

Zhangjiagang, China, 215699

Active, Not Recruiting

31

Research Site

Zhengzhou, China, 450000

Withdrawn

32

Research Site

Zhengzhou, China, 450008

Active, Not Recruiting

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Research Team

A

AstraZeneca Clinical Study Information Center

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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