Study on the Effects of Azeliragon for Patients with Metastatic Pancreatic Cancer Not Responding to Previous Treatments

Sponsor: Cantex Pharmaceuticals

Sponsor score: 0
Inactive

ClinicalTrials ID:NCT05766748

This clinical trial is exploring the safety and potential benefits of a new drug, azeliragon, for patients with metastatic pancreatic cancer who have not responded to previous treatments.

Patient Parameters

Program Overview

The purpose of this study is to evaluate the safety and initial effectiveness of azeliragon, a new treatment for patients with metastatic pancreatic cancer that has not responded to previous therapies. The study is open-label, meaning both the researchers and participants know what treatment is being administered.

Eligibility Criteria

Inclusion Criteria

  • Have a confirmed diagnosis of advanced or metastatic pancreatic cancer that cannot be treated with surgery.
  • Previously treated with chemotherapy regimens like Gemcitabine/Abraxane or FOLFIRINOX.
  • Any side effects from previous chemotherapy, except hair loss, should have improved to a mild level or returned to baseline.
  • Be a male or a non-pregnant, non-breastfeeding female aged between 18 and 80.
  • Have adequate blood counts and organ function as shown by specific blood tests.
  • Have a performance status score of 2 or less, indicating the ability to carry out daily activities with some limitations.
  • Understand the study details and agree to participate by signing an informed consent form.

Exclusion Criteria

  • Have a life expectancy of less than 3 months.
  • Have a performance status score that worsens to more than 2 before starting the study drug.
  • Have active, uncontrolled infections requiring treatment.
  • Are taking certain medications that interfere with the study drug.
  • Have serious medical or psychiatric conditions that could affect safety or study results.
  • Are unable or unwilling to follow study procedures, including taking oral medication.
  • Have digestive issues that affect swallowing or absorbing medication.
  • Are sexually active and not using effective birth control methods if of childbearing potential.
  • Are participating in another interventional clinical trial or have used another investigational drug within 14 days before starting the study drug. Participation in non-interventional studies is allowed.

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