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
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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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