drugset / Trial / NCT06612632

Immunotherapy Rechallenge in Patients with Solid Tumors in Clinical Trials

NCT06612632

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study plans to include approximately 60-100 patients with advanced solid tumors who have progressed on clinical trial drugs. It will use an open-label, single-arm, multi-cohort umbrella design. In the first phase, patients who have progressed during treatment with novel tumor immunotherapy drugs will initially be targeted, combining or sequencing with PD-1 monoclonal antibody therapy. The inclusion criteria for frontline clinical trials are as follows: priority will be given to phase I clinical trials of novel immunotherapeutics as monotherapy, such as tumor vaccines, NK cell therapy, and new immune checkpoint inhibitors. Based on preliminary data, these have shown synergistic effects with PD-1/L1 monoclonal antibodies. In principle, the same investigational drug will only be used in either a combination or sequencing cohort. Subsequently, the study will expand to include patients who have progressed on other clinical trial treatments, combining or sequencing with other immune mechanism drugs.

Timeline

Start
2024-05-24
Primary completion
2026-06
Completion
2028-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Toripalimab Monoclonal antibody 3 mg/kg
Subject Toripalimab Monoclonal antibody 200 mg

Indications