Viewing Study NCT06188650



Ignite Creation Date: 2024-05-06 @ 7:54 PM
Last Modification Date: 2024-10-26 @ 3:17 PM
Study NCT ID: NCT06188650
Status: RECRUITING
Last Update Posted: 2024-01-03
First Post: 2023-12-18

Brief Title: The Efficacy and Safety of Drug Loaded Microsphere Bronchial Artery Chemoembolization DEB-BACE Combined With Anlotinib and Adebelimumab in the Third Line Treatment of Advanced NSCLC a Prospective Single Arm Single Center Exploratory Clinical Study
Sponsor: Ningbo Medical Center Lihuili Hospital
Organization: Ningbo Medical Center Lihuili Hospital

Study Overview

Official Title: The Efficacy and Safety of Drug Loaded Microsphere Bronchial Artery Chemoembolization DEB-BACE Combined With Anlotinib and Adebelimumab in the Third Line Treatment of Advanced NSCLC a Prospective Single Arm Single Center Exploratory Clinical Study
Status: RECRUITING
Status Verified Date: 2023-12
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: The goal of this clinical trial is to learn about Drug loaded microspheres for bronchial artery chemoembolization DEB-BACE combined with anlotinib and adebelimumab in patients with advanced NSCLC after second-line treatment

The main question it aims to answer is

The efficacy and safety of Drug Loading Beads Bronchial Arterial Chemoembolization DEB-BACE combined with Anlotinib and Adebelimumab in the third line treatment of advanced NSCLC

Participants will receive DEB-BACE treatment rest for 1 week and then undergo 1 cycle of treatment with combination of Anlotinib and Adebelimumab With a maximum of 4 DEB-BACE treatments depending on the therapeutic effect followed by continued treatment with Anlotinib and Adebelimumab
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?: False
Is an FDA AA801 Violation?: None