NCT05928299Completed
Integrative Multi-Omics Testing for Immunotherapy Response in Non-Small Cell Lung Cancer
Proteomic and Metabolomic Features Testing for Immunotherapy Response in Non-Small Cell Lung Cancer
Source: ClinicalTrials.gov · Last updated 20 May 2026
Brief summary (registry, in English)
The objective of this study is to use blood and urine proteomic and metabolomic features to monitor lung cancer immunotherapy response.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 150 (actual)
- First submitted
- 8 May 2023
- Start date
- 1 Jan 2020
- Primary completion date
- 31 Dec 2025
- Lead sponsor
- Nanfang Hospital, Southern Medical University
- Diseases
- Lung cancer
- NCT number
- NCT05928299
What you commit to
- Study type: Observational
- Participants enrolled: 150
- From 1 Jan 2020 to the primary completion date, 31 Dec 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Patients with the history of autoimmune disease or immunodeficiency disease;
- Any severe, uncontrolled diseases, including: (1) Active or uncontrolled heart diseases, (2) Renal failure requires hemodialysis or peritoneal dialysis; (3) Liver diseases such as liver cirrhosis, decompensated liver disease, chronic active hepatitis;
- Any severe, uncontrolled urological diseases, or urine total protein \>1.0g/day.
Lab values
- Any severe, uncontrolled metabolic diseases, including uncontrolled diabetes mellitus (fasting blood glucose (FBG)\>10mmol/L);
Who the study is looking for
- Patients who are 18 years or older at the time of signing the informed consent form;
- Patients with histologically or cytologically confirmed non-small cell lung cancer that is metastatic or locally advanced unresectable, not eligible for local curative treatment (Stage IIIB or IV according to AJCC);
- Patients without contraindications for immunotherapy according to CSCO guidelines for Non-Small Cell Lung Cancer (NSCLC) version 2022(No EGFR mutations, ALK or ROS1 rearrangement);
- Patients with at least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors \[RECIST\], version 1.1;
- Patients who have not received systemic treatment in the past, or who have previously received (neo) adjuvant treatment/radical treatment programs and have relapsed for more than 6 months;
- Patients who signed the informed consent and are willing to participate in the study.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Nanfang Hospital Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.