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Modified TOMOX-HAIC in Combination With Sintilimab and Bevacizumab Biosimilar for First-line Treatment of Advanced Hepatocellular Carcinoma - Trial NCT06285019

Access comprehensive clinical trial information for NCT06285019 through Pure Global AI's free database. This Phase 2 trial is sponsored by Fudan University and is currently Recruiting. The study focuses on Hepatocellular Carcinoma. Target enrollment is 65 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06285019
Phase 2
Recruiting
procedure
Trial Details
ClinicalTrials.gov โ€ข NCT06285019
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Modified TOMOX-HAIC in Combination With Sintilimab and Bevacizumab Biosimilar for First-line Treatment of Advanced Hepatocellular Carcinoma
Efficacy and Safety of Modified Hepatic Artery Infusion Chemotherapy (TOMOX-HAIC) in Combination With Sintilimab and Bevacizumab Biosimilar for the First-line Treatment of Advanced Hepatocellular Carcinoma: a Prospective, Single-arm, Phase II Clinical Study

Study Focus

Hepatocellular Carcinoma

TOMOX-HAIC

Interventional

procedure

Sponsor & Location

Fudan University

Shanghai, China

Timeline & Enrollment

Phase 2

Dec 01, 2023

Dec 31, 2025

65 participants

Primary Outcome

objective response rate (ORR)

Summary

This is a single-center, single-arm, phase II clinical study, to explore the efficacy and
 safety of modified TOMOX-HAIC combined with sintilimab and bevacizumab biosimilar as first
 line treatment in patients with advanced hepatocellular carcinoma.

ICD-10 Classifications

Malignant neoplasm: Hepatoblastoma
Malignant neoplasm: Liver cell carcinoma
Malignant neoplasm: Other specified carcinomas of liver
Malignant neoplasm: Liver, unspecified
Malignant neoplasm: Hepatic flexure

Data Source

ClinicalTrials.gov

NCT06285019

Non-Device Trial