Viewing Study NCT06311851



Ignite Creation Date: 2024-05-06 @ 8:15 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06311851
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-01
First Post: 2024-03-06

Brief Title: Transarterial Chemoembolization TACE Plus Bevacizumab for Liver Metastases
Sponsor: Pardis Noor Medical Imaging and Cancer Center
Organization: Pardis Noor Medical Imaging and Cancer Center

Study Overview

Official Title: An Open-Label Pilot Study to Evaluate Efficacy and Safety of Bevacizumab Via Transarterial Chemoembolization TACE in Patients With Liver Metastases
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-03
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: Trans arterial chemoembolization TACE has emerged as a treatment option for chemotherapy-refractory diseases in Liver metastases By delivering chemotherapy agents directly to the tumor site TACE can maximize local drug concentrations and reduce systemic adverse reactions Bevacizumab is a monoclonal antibody that functions as an angiogenesis inhibitor It works by slowing the growth of new blood vessels by inhibiting vascular endothelial growth factor A VEGF-A The application of Bevacizumab during TACE has not been reported In this study we will evaluate the the overall survival OSefficacy and safety of the application of Bevacizumab during TACE in patients with Liver Metastases by designing an open single-arm phase II clinical study
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