Viewing Study NCT06492421



Ignite Creation Date: 2024-07-17 @ 11:50 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06492421
Status: RECRUITING
Last Update Posted: 2024-07-09
First Post: 2024-07-02

Brief Title: Neoadjuvant Intra-tumor Double Immunotherapy for Lung Cancer
Sponsor: Second Affiliated Hospital of Guangzhou Medical University
Organization: Second Affiliated Hospital of Guangzhou Medical University

Study Overview

Official Title: Phase II Study of Neoadjuvant CT-Guided Intra-tumor Double Checkpoint Blockades for Untreated Stage I-IIIA Non-Small Cell Lung Cancers Amenable for Surgical Resection
Status: RECRUITING
Status Verified Date: 2024-07
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: This phase II trial studies how well intra-tumor injection of double checkpoint inhibitors work when given alone and in combination with chemotherapy orand bevacizumab in treating patients with previously untreated stage I-IIIA non-small cell lung cancer Immunotherapy with monoclonal antibodies such as ipilimumab pembrolizumab or durvalumab may help the bodys immune system attack the tumor and may interfere with the ability of tumor cells to grow and spread Drugs used in interventional radiological chemotherapy such as idabubicin can directly kill the cancer cell and release tumor antigens to activate DC function in situ Giving intra-tumor injection of checkpoints inhibitors with or without chemotherapy andor bevecizumab may work better than in vein infusion of the drugs in treating patients with non-small cell lung cancer
Detailed Description: Antibodies against CTLA4 PD1 or PDL1 are representative drugs for the check-points inhibitory agents and their clinical indications have been approved in various types of tumors including advanced melanoma non-small cell lung cancer renal cell carcinoma and classical Hodgkins lymphoma and late recurrent head and neck squamous cell carcinoma patients et al Those drugs are regularly systemically administrated by vein infusion however local delivery of those drugs via interventional radiology technique including trans-artery or intra-tumor injection may increase the local drug concentration of the tumor improve the efficacy and reduce systemic adverse reactions CTLA4 antibody ipilimumab has been widely effectively using to combine with PD1 or PDL1 antibody and this study is to combine ipilimumab and PD1 antibody or PDL1 antibody so called double checkpoint inhibitors combination therapy as neoadjuvant therapy for NSCLC via intra-tumor admistration To the investigators knowledge no studies have been developed on the safety efficacy and survival benefit of the double checkpoint inhibitors combination therapy for cancer patients as neoadjuvant treatment via intra-tumor delivery This phase II clinical trial is designed to assess the safety and survival benefit of ipilimumab and pembrolizumab or durvalumab combination with or without chemodrug andor bevacizumab as neoaduvant therapy on patients with NSCLC including safety pCR mPR PFS ORR DCR and median survival time

Study Oversight

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