Viewing Study NCT06485466



Ignite Creation Date: 2024-07-17 @ 10:41 AM
Last Modification Date: 2024-10-26 @ 3:33 PM
Study NCT ID: NCT06485466
Status: RECRUITING
Last Update Posted: 2024-07-03
First Post: 2024-06-22

Brief Title: TACE Plus Camrelizumab and Apatinib for Unresectable Hepatocellular Carcinoma
Sponsor: Guohui Xu
Organization: Sichuan Cancer Hospital and Research Institute

Study Overview

Official Title: Transarterial Chemoembolization Plus Camrelizumab and Apatinib for Unresectable Hepatocellular Carcinoma a Randomised Open Label Multicenter Controlled Trial
Status: RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Hepatocellular carcinoma HCC is the sixth most common cancer and the third most common cause of cancer-related death worldwide The majority of patients with HCC are diagnosed as intermediate or advanced stage disease and not eligible for curative treatments including transplantation resection and ablation Transarterial chemoembolization TACE is recommended as first-line treatment for patients with intermediate-stage HCC while it is also widely used in the unresectable HCC

The clinical efficacy and safety in advanced HCC patients of camrelizumab plus apatinib were reported in phase 3 trial CARES-310 Camrelizumab plus apatinib with a median progression-free survival of 57 months and a median overall survival of 221 months in advanced HCC

This study is randomized open-label multicenter controlled trial which was focused in initial BCLC-BC HCC patients This study aimed to compare the efficacy and safety of TACE plus programmed death-1 inhibitor camrelizumab and anti-angiogenic therapy apatinib with camrelizumab plus apatinib
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None