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Clinical Trials in China / NCT06824792
Starting soon Phase 4

Optimal Standard Treatment Selection for Solid Tumor Patients by Biologically-informed Multi-agent System

NCT06824792 · tracked via the Priya Life Science China tracker
Sponsor
NING LI
Phase
Phase 4
Started
2025-03-01
Last updated
2025-02-13

Condition(s) studied

Advanced Solid Tumors

Investigational drug(s) / intervention(s)

Biologically-informed multi-agent system (Quasar) including targeted drugs Osimertinib, chemotherapy pemetrexed, immunotherapy pembrolizumab et al. approved by China CDE.

Biologically-informed multi-agent system (Quasar) including targeted drugs Osimertinib, chemotherapy pemetrexed, immunotherapy pembrolizumab et al. approved by China CDE.: Quasar is a biologically-informed multi-agent system developed based on multi-omics and multi-modal data. By integrating multidimensional information such as patients' demographic, clinical, and omics data (including DNA genotyping, whole-exome sequencing, transcriptome sequencing, etc.), it prioritizes standard treatment plans and recommends the optimal personalized treatment plan. Including targeted drugs, chemotherapy, immunotherapy approved by China CDE.

Study summary

This study is an exploratory cohort study conducted under real-world conditions, aiming to evaluate the feasibility of an artificial intelligence (AI)-guided standard treatment selection model for advanced solid tumors, as well as its superiority compared to clinician-selected treatment plans. A multi-agent system based on multimodal AI models will rank the priority of standard treatment options based on the personalized information of the patients, including including demographics, clinical information, and multi-omics data. The final treatment plan will be jointly selected by the patient and the clinician from the AI-recommended options, thereby delivering a personalized treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Voluntarily participate in the clinical study, fully understand and be informed about the study, sign the informed consent form, and be willing and able to comply with and complete all trial procedures. * Aged ≥18 years, no gender restrictions. * Patients with advanced or metastatic malignant tumors confirmed by histology or cytology. * Able to provide tumor tissue and peripheral blood samples for multi-omics testing, or able to provide qualified whole-exome sequencing and transcriptomics data. Exclusion Criteria: * As assessed by the investigator, no standard treatment is available, or the patient is unsuitable for guideline-recommended anti-tumor therapies. * Other conditions deemed unsuitable for participation in this study by the investigator.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cancer Institute and Hospital, Chinese Academy of Medical Sciences (Langfang Branch) Langfang Hebei

More NING LI trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06824792 on ClinicalTrials.gov ↗ ← All trials in China