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NCT07587034Not yet recruitingPhase 1/2

HAIC-TACE Plus Apatinib and Camrelizumab for Liver Cancer

MATCH-001: A Multicenter, Open-Label, Randomized Controlled Trial of Hepatic Arterial Infusion Chemotherapy Followed by Transarterial Chemoembolization Combined With Apatinib and Camrelizumab in Patients With Intermediate and Advanced Hepatocellular Carcinoma

Source: ClinicalTrials.gov · Last updated 20 May 2026

Brief summary (registry, in English)

To provide evidence-based medical evidence for the optimized combination strategy of local and systemic therapies.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
315 (estimated)
First submitted
8 May 2026
Start date
Jun 2026
Primary completion date
Dec 2029
Lead sponsor
Shanghai Zhongshan Hospital
NCT number
NCT07587034

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 315
  • From Jun 2026 to the primary completion date, Dec 2029
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior transarterial chemoembolization (TACE) or other local therapies for HCC (except bridging liver transplantation).
  • Administration of radiotherapy or other interventions during the trial that prevent efficacy evaluation.

Other illness

  • 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.
  • Concurrent other malignancies or history of other malignancies within the past 3 years.
  • 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.
  • BCLC Staging: Barcelona Clinic Liver Cancer staging system, a globally recognized framework for HCC prognosis and treatment decision-making.

Lab values

  • 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.).

Other

  • Alcohol abuse or pregnancy.
  • Inability to cooperate with interventional procedures.
  • Presence of distant metastasis.
  • Main portal vein tumor thrombus accompanied by impaired portal venous blood flow and collateral circulation.
    • Withdrawal Criteria
  • Identification of non-compliance with the study protocol during the trial.
  • Discontinuation of treatment due to severe adverse reactions (excluded from efficacy analysis but included in adverse reaction statistics).
  • Patient or representative withdraws informed consent or requests to stop treatment.
  • 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.
  • mRECIST: Abbreviation for Modified Response Evaluation Criteria in Solid Tumors, the standard for assessing treatment response in HCC, widely used in clinical trials.
  • 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.

Who the study is looking for

  • Age 18-80 years.
  • 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.
  • 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.
  • Child-Pugh liver function grade A or well-compensated grade B (score ≤7).
  • ECOG Performance Status (PS) score 0-1.
  • Expected survival time ≥12 weeks.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.