A Study to Evaluate SHR-1210 in Subjects With Advanced HCC

Hengrui Medicine

Status and phase: Completed; Phase 2

Conditions: Hepatocellular Carcinoma Non-Resectable

Treatments: Biological: SHR-1210

Study type: Interventional

Funder types: Industry

Identifiers

NCT02989922

SHR-1210-II/III-HCC

Details and patient eligibility

About

This a randomized controlled Phase 2/3 study to evaluate the efficacy and safety of SHR-1210 in subjects with advanced HCC who failed or intolerable to prior systemic treatment. The primary study hypothesis is that SHR-1210 treatment improves Objective Response Rate and Overall Survival when compare with SOC.

Full description

In June 2017, this study was revised to expand the Phase 2 part to enroll more subjects and remove the Phase 3 part under the same protocol. A Phase 3 study will be initiated separately.

Enrollment: 220 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Histologically confirmed HCC in advanced stage; not suitable to surgery or local regional treatment; with at least one measurable lesion per RECIST 1.1
2. Failed or intolerable to at least one prior systemic treatment for advanced HCC
3. ECOG Performance Status of 0 or1
4. Child-Pugh Class A or B with 7 points
5. Life Expectancy of at least 12 weeks
6. HBV DNA<500 IU/ml
7. Adequate organ function
8. Male or female participants of childbearing potential must be willing to use an adequate method of contraception starting with the first dose of study drug through 60 days for female subjects and 120 days for male subjects after the last dose of study drug

Exclusion criteria

1. Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC
2. Known liver transplant or plan to transplant
3. GI hemorrhage with 6 months
4. History or current brain metastases
5. Active known, or suspected autoimmune disease

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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220 participants in 2 patient groups

SHR-1210 Q2W

Experimental group

Description:

Subjects receive SHR-1210 intravenous at the dose 3mg/kg on Day 1 every 2 weeks

Treatment:

Biological: SHR-1210

SHR-1210 Q3W

Experimental group

Description:

Subjects receive SHR-1210 intravenous at the dose 3mg/kg on Day 1 every 3 weeks

Treatment:

Biological: SHR-1210