drugset / Trial / NCT06692491

Study of Precision Treatment for Rare Tumours in China Guided by PDO and NGS

NCT06692491

Phase 2 Not yet recruiting 200 enrolled Peking University Shenzhen Hospital
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The objective of this Phase II, open-label, multicenter, non-randomised controlled clinical trial is to guide precision treatment for patients with rare tumours based on Patient-Derived Organoids/Next-Generation Sequencing drug screening.

Timeline

Start
2025-01-01
Primary completion
2027-12-31
Completion
2029-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Adebrelimab Monoclonal antibody 20 mg/kg
Subject Alectinib Small molecule 600 mg
Subject Atezolizumab Monoclonal antibody 1200 mg
Subject Camrelizumab Monoclonal antibody 200 mg
Subject Cisplatin Other / unclassified 90 mg/m2
Subject Durvalumab Monoclonal antibody 10 mg/kg
Subject Entrectinib Small molecule 600 mg
Subject Envafolimab Monoclonal antibody 150 mg
Subject Epirubicin Small molecule 90 mg/m2
Subject Gemcitabine Small molecule 1000 mg/m2
Subject Imatinib Small molecule 400 mg
Subject Irinotecan Small molecule 125 mg/m2
Subject Nivolumab Monoclonal antibody 3 mg/kg
Subject Osimertinib Small molecule 80 mg
Subject Paclitaxel Small molecule 260 mg/m2
Subject Palbociclib Small molecule 125 mg
Subject Pamiparib Small molecule 60 mg
Subject Pembrolizumab Monoclonal antibody 200 mg
Subject Pyrotinib Small molecule 400 mg
Subject Savolitinib Small molecule 300 mg
Subject Serplulimab Monoclonal antibody 3 mg/kg
Subject Sintilimab Monoclonal antibody 200 mg
Subject Tislelizumab Monoclonal antibody 200 mg
Subject Toripalimab Monoclonal antibody 240 unknown
Subject Vemurafenib Small molecule 960 mg
Subject Vinorelbine Small molecule 25 mg/m2
Subject Vinorelbine Small molecule 30 mg/m2
Subject fluorouracil Small molecule 600 mg/m2

Indications

No indication recorded.