TATE Versus TACE in Intermediate Stage HCC

• Status: Active, not recruiting
• Trial end date: 2021-12-31
• Target enrollment: 0
• Participant gender: All

Summary

An open label randomized study to compare TATE versus TACE in patients with intermediate stage Hepatocellular carcinoma who are not suitable for surgical resection or radiofrequency ablation. The primary endpoint is Progression Free Survival. Secondary endpoints including CR rate, Time to embolization failure, Duration of CR, OS, ORR, local control rate, time to local recurrence and duration to local recurrence. The study treatment is to compare Tirapazamine versus doxorubicin when combined with trans-arterial embolization. Study plans to enroll 134 patients in 1:1 randomization for TATE or TACE. MRI will be used to assess efficacy using a central radiological review for the final analysis.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Teclison Ltd.
• Treatments: Doxorubicin; Liposomal doxorubicin; Tirapazamine

Criteria

1. Confirmed diagnosis of HCC by imaging criteria per American Association for the Study of Liver Diseases (AASLD) criteria.

2. Patients with single or multiple HCC who are unsuitable for surgical resection or RFA, but suitable for embolization.

3. ECOG score 0-1. Child-Pugh score up to B7.

4. Patients should have measurable tumor lesion(s) by contrast MRI.

5. Patients have adequate normal organ function and suitable laboratory criteria.

6. Men and women of child-bearing age need to commit to using two levels of contraception simultaneously to avoid pregnancy.

Exclusion Criteria:

1. Patients who have had a liver transplantation.

2. Patients who have uncontrolled major medical problems such as cardiac, pulmonary (COPD requiring constant oxygen), renal (creatinine over 2.0) diseases, active infectious diseases (except chronic Hepatitis B or C), or non-healing ulceration.

3. Patients who have any clinical evidence of hypoxia with O2 saturation less than 92% on room air.

4. Patients with evidence of arterial insufficiency or microangiopathy in any organ due to any reason, which could lead to distal extremity hypoxia, as evidenced by any gangrenous change in distal limbs or requiring resection for this reason.

5. Patients with poorly controlled HBV infection.

6. Patients on interferon treatment need to have at least 2-week washout period from Day 1.

7. Patients with major gastrointestinal bleeding in the prior 2 months of enrollment or known diagnosis of cancer other than HCC.

8. Pregnant or lactating women.