Study on Dupilumab for Treating Metastatic Non-Small Cell Lung Cancer (NSCLC)

Sponsor: Thomas Marron

Sponsor score: 0
Inactive

ClinicalTrials ID:NCT05013450

This clinical trial is testing the safety and effectiveness of combining Dupilumab with PD-(L)1 blocking drugs for patients with metastatic non-small cell lung cancer (NSCLC) that has returned or not responded to previous treatments.

Patient Parameters

Program Overview

This study aims to find out if adding Dupilumab to existing PD-(L)1 blocking treatments can help patients with metastatic non-small cell lung cancer (NSCLC) who have not responded to or have relapsed after previous treatments. The trial will assess the safety and tolerability of this combination therapy in patients who have already tried PD-(L)1 therapies.

Eligibility Criteria

Inclusion Criteria

  • Must have a confirmed diagnosis of non-small cell lung cancer (NSCLC).
  • Cancer must have progressed after previous treatment with PD-1 or PD-L1 targeted therapy.
  • Can have had only one or no other treatments since the last PD-(L)1 therapy.
  • Must be willing to provide blood samples and undergo tumor biopsies as part of the study.
  • Must be 18 years or older.
  • Must have an ECOG performance status of 0 to 2, unless a long-term disability is present that does not affect response to therapy.
  • Women of childbearing potential and men must agree to use effective contraception during the study and for three months after treatment.
  • Must be able to understand and sign a consent form.

Exclusion Criteria

  • Cannot have had chemotherapy within 14 days before starting the study treatment.
  • Palliative radiotherapy is allowed if it is in the patient's best interest.
  • Cannot have uncontrolled illnesses, such as ongoing infections, heart failure, or unstable mental health conditions.
  • Cannot be pregnant or nursing due to potential risks to the baby.
  • Cannot have an immune deficiency or be on immunosuppressive therapy within seven days before starting the study treatment, except for stable low-dose steroids.
  • Cannot have active autoimmune diseases requiring treatment in the past year, except for replacement therapies like insulin.
  • Cannot have conditions or treatments that might interfere with the study or are not in the patient's best interest.
  • Cannot have HIV with a detectable viral load or unstable treatment.
  • Cannot have active Hepatitis B or C infections, unless controlled with treatment.
  • Cannot have had a bone marrow or organ transplant.
  • Cannot have received a live vaccine within 30 days before starting the study.
  • Cannot have allergies to protein-based treatments.
  • Cannot have unresolved immune-related side effects from previous immunotherapy.
  • Cannot have a history of lung diseases like interstitial lung disease or pneumonitis from previous cancer treatments.

Get This Program In Your Inbox

Receive detailed information about this treatment opportunity to review with your healthcare provider.