Clinical Trials in China / NCT07713290
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
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Beijing Ditan Hospital, Capital Medical University | Beijing | Beijing Municipality | |
| Beijing You An Hospital | Beijing | Beijing Municipality | |
| First Hospital of Shanxi Medical University | Taiyuan | Shanxi |
More Beijing Gene Key Life Technology Co., Ltd trials in China
Other trials for the same condition
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