Clinical Trials Directory

Trials / Terminated

TerminatedNCT03951012

Use Peripheral Blood Proteomics to Predict the Treatment Response and Toxicities in NSCLC Immunotherapy

Status
Terminated
Phase
Study type
Observational
Enrollment
29 (actual)
Sponsor
Muhammad Furqan · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

Summary

Peripheral blood contains enormous quantity of biological information that can improve our patient care. Investigators plan to use proteomics from serum to study its value in predicting the therapeutic response and toxicities of immunotherapy in non-small cell lung cancer (NSCLC).

Detailed description

An extra tube of blood for research will be collected from consented subjects prior to the initiation of anti-PD-1/L1 based immunotherapy, either single agent or in combination with chemotherapy. The blood will be coded, processed and sent for analysis. Results of analysis will be correlated with clinical data to see whether serum proteomics can be a good therapeutic predictor for future studies and treatments of NSCLC.

Conditions

Interventions

TypeNameDescription
PROCEDUREBlood drawParticipants will be approached during their regular clinic visits and asked if an extra tube of blood may be collected prior to the treatment. If consent is not obtained before this visit, a participant will be asked later in the same day. The amount of blood collected will be 2 teaspoons (10mL).

Timeline

Start date
2019-04-15
Primary completion
2022-08-30
Completion
2023-09-08
First posted
2019-05-15
Last updated
2023-10-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03951012. Inclusion in this directory is not an endorsement.