Interstitial Lung Disease Clinical Trials

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A Single-cell Approach to Identify Biomarkers of Pulmonary Toxicity for Immune Checkpoint Blockade

Status: Recruiting
Location: See location...
Intervention Type: Drug, Radiation
Study Type: Observational
SUMMARY

The main goal of this prospective non-interventional exploratory monocentric study is to characterize the immune cell composition of bronchoalveolar lavage (BAL) fluid from cancer patients experiencing cancer therapy-induced pneumonitis on a single-cell scale. These mechanistic insights can directly lead to putative diagnostic biomarkers and therapeutic targets. A second highly clinically relevant hypothesis is that single-cell profiling of blood samples will reveal circulating biomarkers of ICB toxicity, making non-invasive diagnosis feasible.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 120
Healthy Volunteers: f
View:

• Adult M/F/X (\>= 18 years)

• Patients receiving or having received treatment per guidelines

• Patients undergoing bronchoscopy with BAL, for possible cancer treatment-induced pneumonitis

• Not included in other clinical trials

• Signed informed consent form

Locations
Other Locations
Belgium
Universitaire Ziekenhuizen Leuven
RECRUITING
Leuven
Contact Information
Primary
Els Wauters, MD, PhD
els.wauters@uzleuven.be
+3216340942
Time Frame
Start Date: 2020-02-01
Estimated Completion Date: 2025-01-31
Participants
Target number of participants: 60
Treatments
ICI-pneumonitis
Cancer patients experiencing ICI-pneumonitis
Radiotherapy induced pneumonitis
Cancer patients experiencing RT-pneumonitis
TKI-induced pneumonitis
Cancer patients experiencing TKI-induced pneumonitis
Sponsors
Leads: Universitaire Ziekenhuizen KU Leuven
Collaborators: KU Leuven

This content was sourced from clinicaltrials.gov