New combo therapy aims to tackle advanced liver cancer
NCT ID NCT07587034
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This trial is testing a new way to treat intermediate and advanced liver cancer. It combines two liver-directed procedures (HAIC and TACE) with two drugs (apatinib and camrelizumab) to see if this approach works better than other combinations. The study will involve 315 adults with liver cancer who cannot have surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- apatinib and camrelizumab
- What this could lead to
- If successful, this could lead to a more effective treatment strategy for people with intermediate to advanced liver cancer, potentially extending life and controlling tumor growth.
- What could go wrong
- This is an early-phase trial (Phase 1/2) with a small number of participants, so results may not apply to everyone. The combination therapy also carries risks of side effects from the drugs and procedures.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 315 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria 1. Age 18-80 years. 2. Diagnosed with hepatocellular carcinoma (HCC) in accordance with the Standardization for Diagnosis and Treatment of Primary Hepatic Carcinoma (2024 Edition) issued by the National Health Commission of the People's Republic of China. 3. BCLC stage B or C, with no indication or refusal of surgical treatment, and measurable lesions meeting the mRECIST (Modified Response Evaluation Criteria in Solid Tumors) criteria on baseline imaging. 4. Child-Pugh liver function grade A or well-compensated grade B (score ≤7). 5. ECOG Performance Status (PS) score 0-1. 6. Expected survival time ≥12 weeks. Exclusion Criteria 1. Prior transarterial chemoembolization (TACE) or other local therapies for HCC (except bridging liver transplantation). 2. Active viral hepatitis (hepatitis B or C) with pre-treatment viral load \>100 IU/mL (positive for HCV RNA or HBV DNA) or without consistent antiviral therapy. 3. Alcohol abuse or pregnancy. 4. Concurrent other malignancies or history of other malignancies within the past 3 years. 5. Renal dysfunction (creatinine \[Cr\] \>2 mg/dL or creatinine clearance \[CCr\] \<30 mL/min) or severe organic diseases of vital organs (heart, lung, brain, etc.). 6. Inability to cooperate with interventional procedures. 7. Presence of distant metastasis. 8. Main portal vein tumor thrombus accompanied by impaired portal venous blood flow and collateral circulation. Withdrawal Criteria 1. Identification of non-compliance with the study protocol during the trial. 2. Administration of radiotherapy or other interventions during the trial that prevent efficacy evaluation. 3. Discontinuation of treatment due to severe adverse reactions (excluded from efficacy analysis but included in adverse reaction statistics). 4. Patient or representative withdraws informed consent or requests to stop treatment. 5. Loss to follow-up or death of the patient. Key Terminology Notes * National Health Commission of the People's Republic of China: Official English name of the Chinese health authority, consistent with government documentation. * Standardization for Diagnosis and Treatment of Primary Hepatic Carcinoma (2024 Edition) : Translated title of the 2024 national guideline for HCC diagnosis and treatment, aligning with the 2022 edition's official English translation published in Cancer Research on Prevention and Treatment. * mRECIST: Abbreviation for Modified Response Evaluation Criteria in Solid Tumors, the standard for assessing treatment response in HCC, widely used in clinical trials. * BCLC Staging: Barcelona Clinic Liver Cancer staging system, a globally recognized framework for HCC prognosis and treatment decision-making. * Child-Pugh Score: A widely used tool to assess liver function in patients with cirrhosis, with grades A (5-6 points), B (7-9 points), and C (10-15 points). * ECOG PS Score: Eastern Cooperative Oncology Group Performance Status, a scale from 0 (fully active) to 5 (dead) used to evaluate a patient's ability to perform daily activities.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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