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NCT03968419 · ClinicalTrials.gov registry record · Phase 2

This Study Will Evaluate the Effect of Canakinumab or Pembrolizumab Given as Monotherapy or in Combination as Neo-adjuvant Treatment for Subjects With Early Stages NSCLC.

A Phase 2 study, sponsored by Novartis Pharmaceuticals.

Terminated
Registry status
Phase 2
Development phase
88
Enrollment target

NCT03968419 is a Phase 2 study that was terminated before completion, run by Novartis Pharmaceuticals. The registered enrollment target is 88 participants.

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The verdict

NCT03968419, a Phase 2 study, was terminated before completion, sponsored by Novartis Pharmaceuticals.

TERMINATED
Registry status
Phase 2
Development phase
88 participants
Enrollment target

Study Summary

The purpose of this study was to evaluate the major pathological response (MPR) rate of canakinumab given as a neoadjuvant treatment, either as single agent or in combination with pembrolizumab, in addition to evaluate the MPR of pembrolizumab as a single agent and the dynamic of the tumor microenvironment changes on treatment.

Interventions

  • DRUG Pembrolizumab
  • DRUG Canakinumab

Trial Details

FieldValue
Enrollment Target 88 participants
Start Date 2019-11-05
Est. Completion 2022-08-15
Phase Phase 2

Sponsor

Novartis Pharmaceuticals

1,375 total trials

What the Registry Record Tells You About NCT03968419

The ClinicalTrials.gov registry entry for NCT03968419 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 88 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Pembrolizumab is the first listed.

NCT03968419 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03968419 about?

NCT03968419 is a clinical study titled "This Study Will Evaluate the Effect of Canakinumab or Pembrolizumab Given as Monotherapy or in Combination as Neo-adjuvant Treatment for Subjects With Early Stages NSCLC.". The purpose of this study was to evaluate the major pathological response (MPR) rate of canakinumab given as a neoadjuvant treatment, either as single agent or in combination with pembrolizumab, in addition to evaluate the MPR of pembrolizumab as a single agent and the dynamic of the tumor microenvi...

What is the current status of trial NCT03968419?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 88 participants. The study started on 2019-11-05. Estimated completion is 2022-08-15.

What interventions are being tested in trial NCT03968419?

The interventions under investigation include: Pembrolizumab (DRUG), Canakinumab (DRUG).

Who is sponsoring clinical trial NCT03968419?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.