Olanzapine Impact on First-line Immunotherapy for Advanced EGFR-negative NSCLC

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorSecond Affiliated Hospital of Nanchang University

About this trial

Clinical Trial

The objective of this clinical trial is to determine whether antidepressant medications, such as olanzapine, in combination with immune checkpoint inhibitors are more effective than the use of immune checkpoint inhibitors alone. The main questions it aims to answer are:

Is the combination therapy of antidepressant medication with immune checkpoint inhibitors more efficacious than the therapy with immune checkpoint inhibitors alone? What medical issues might participants encounter when treated with the combination of antidepressant medication and immune checkpoint inhibitors?

Participants will:

Take olanzapine in combination with immune checkpoint inhibitors or immune checkpoint inhibitors alone for 2 months.

Visit the clinic for check-ups and tests every two weeks, and have follow-up visits every six weeks after the treatment ends.

Keep a record of their symptoms and disease progression.

Eligibility criteria

Qualifiers

Participants voluntarily enroll in this study and sign an informed consent form, with good compliance and cooperation with follow-up.

Age is over 18 years old (including 18 years old) and under 75 years old (including 75 years old).

ECOG score: 0-2 points.

Expected survival is no less than 3 months.

Disqualifiers

Previously used any EGFR tyrosine kinase inhibitors;

Previously received any chemotherapy for lung cancer;

Previously received any radiotherapy for lung cancer (except palliative radiotherapy for bone metastases);

Within 4 weeks prior to the first administration of the study drug, the subject had undergone major surgery;

Trial design

Treatments tested in this trial

  • Olanzapine
  • Nivolumab

Treatment groups

156 Participants
are divided into 2 treatment groups