RecruitingPhase 1Phase 2NCT05187338

Triplex Checkpoint Inhibitors Therapy for Advanced Solid Tumors

Triplex CTLA4/PD1/PDL1 Checkpoint Inhibitors Combination Therapy for Advanced Solid Tumors


Sponsor

Second Affiliated Hospital of Guangzhou Medical University

Enrollment

100 participants

Start Date

Nov 1, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

This trial is designed to investigate the safety, response rates and survival outcomes of patients with advanced solid tumors by infusion of CTLA4, PD1 and PDL1 antibodies combination through venous (IV), artery (IA) or intra-tumor (IT).


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing a three-drug immunotherapy combination (triple checkpoint inhibitors) delivered via a procedure that targets the blood supply to liver tumors (hepatic arterial infusion) in patients with advanced solid tumors. The aim is to boost the immune system's attack on the cancer. **You may be eligible if...** - You are 18 or older with a confirmed cancer diagnosis - You have at least one tumor that can be measured on imaging - You are in reasonably good health (ECOG score less than 2) - Your liver, kidney, and blood counts are within acceptable ranges **You may NOT be eligible if...** - You are currently enrolled in another drug trial - You have uncontrolled fluid in the abdomen (ascites), confusion from liver disease, or bleeding from esophageal or stomach varices - You have another active cancer or history of malignancy - You are pregnant or breastfeeding - You have uncontrolled blood pressure, heart disease, or diabetes Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGipilimumab +pembrolizumab +durvalumab

This study has 3 subgroups: 1. Ipilimumab +pembrolizumab +durvalumab is administrated with a total dose of 1-2mg/kg via vein, every 3 weeks. 2. Ipilimumab +pembrolizumab +durvalumab is administrated with a total dose of 1-2mg/kg via sustained (10min) micro-pump infusion via artery, every 3 weeks. 3. Ipilimumab +pembrolizumab +durvalumab is administrated with a total dose of 50-150mg via intra-tumor fine needle injection in 5 min, every 3 weeks.


Locations(1)

The Second Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, China

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NCT05187338


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