Ireland
--:--IST
Active, not recruiting Phase 1

A Phase 1b Study of GKL-006 Injection in Patients With Unresectable Hepatocellular Carcinoma

NCT07713290 · tracked via the Priya Life Science China tracker
Phase
Phase 1
Started
2025-04-03
Last updated
2026-07-20

Condition(s) studied

Hepatocellular Carcinoma (HCC)Unresectable Hepatocellular Cancer

Investigational drug(s) / intervention(s)

GKL-006 Injection →Transarterial chemoembolization (TACE)

GKL-006 Injection: An iNKT cell therapy

Transarterial chemoembolization (TACE): A standard locoregional therapy for hepatocellular carcinoma

Study summary

This is a Phase 1b study of GKL-006 Injection in patients with unresectable hepatocellular carcinoma.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Voluntarily participates in the study and provides written informed consent. * Has pathologically, cytologically, or radiologically confirmed unresectable hepatocellular carcinoma. * Has CNLC stage II to IIIa disease. * Has not received transarterial chemoembolization within 6 months before screening. * Has at least one measurable lesion according to mRECIST. * Child-Pugh class A or B. * ECOG performance status of 0 - 2. * Has not received radiotherapy, chemotherapy, targeted therapy, or immunosuppressive therapy within 4 weeks before screening. Exclusion Criteria: * Has a known allergy to the investigational product or related components, including human serum albumin. * Has another incurable malignancy within 5 years before screening or concurrently, except for cured basal cell carcinoma of the skin, carcinoma in situ, or breast cancer without recurrence for more than 3 years after radical surgery. * Has a previous diagnosis of mixed or rare histologic subtypes, including fibrolamellar hepatocellular carcinoma, sarcomatoid hepatocellular carcinoma, or combined hepatocellular-cholangiocarcinoma. * Has major vascular invasion on imaging. * Has hepatic encephalopathy within 4 weeks before screening. * Has clinically symptomatic ascites or pleural effusion requiring drainage, or has undergone thoracic or abdominal fluid drainage within 2 weeks before enrollment.

Primary outcome measure(s)

  • Incidence and Severity of Treatment-Related Adverse Events and Safety/Tolerability Risks — From the start of study treatment through 14 days after the fourth treatment; treatment-related adverse events will continue to be assessed according to the study protocol.
    Treatment-related adverse events and laboratory abnormalities will be assessed and graded according to NCI CTCAE v5.0. Safety and tolerability risks include study treatment-related adverse events or laboratory abnormalities occurring.

Trial sites (3)

FacilityCityRegionStatus
Beijing Ditan Hospital, Capital Medical University Beijing Beijing Municipality
Beijing You An Hospital Beijing Beijing Municipality
First Hospital of Shanxi Medical University Taiyuan Shanxi
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07713290 on ClinicalTrials.gov ↗ ← All trials in China