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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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nanfang Hospital
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.