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RECRUITING

Using Ex Vivo Tumoroids To Predict Immunotherapy Response In NSCLC

NCT05332925 · View on ClinicalTrials.gov ↗

Study Summary

To test whether it is feasible to perform the 3D-EX functional predictive response bioassay in the context of patients with advanced/metastatic NSCLC receiving immune checkpoint inhibitors in the standard of care clinical setting.

Interventions

  • DRUG Standard of care immune checkpoint inhbitors

Study Locations (2)

Kansas

  • The University of Kansas Cancer Center (KUCC) — Fairway
  • The University of Kansas Cancer Center, Westwood Campus — Kansas City

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2022-07-21
Est. Completion 2027-02

Sponsor

Jun Zhang, MD, PhD

2 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05332925

The ClinicalTrials.gov registry entry for NCT05332925 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Jun Zhang, MD, PhD, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Lung Cancer appearing as the primary indexed condition, and to 1 intervention — of which Standard of care immune checkpoint inhbitors is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05332925 reports 2 study locations spanning 1 distinct geographic area — top geographies include Kansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05332925 about?

NCT05332925 is a clinical study titled "Using Ex Vivo Tumoroids To Predict Immunotherapy Response In NSCLC". To test whether it is feasible to perform the 3D-EX functional predictive response bioassay in the context of patients with advanced/metastatic NSCLC receiving immune checkpoint inhibitors in the standard of care clinical setting.

What is the current status of trial NCT05332925?

This trial is currently recruiting. The enrollment target is 25 participants. The study started on 2022-07-21. Estimated completion is 2027-02.

What conditions does trial NCT05332925 study?

This clinical trial studies the following conditions: Lung Cancer, NSCLC, NSCLC Stage IV. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05332925?

The interventions under investigation include: Standard of care immune checkpoint inhbitors (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05332925?

This trial is sponsored by Jun Zhang, MD, PhD, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05332925 being conducted?

This trial has 2 study locations across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial