About this trial
The goal of the current pilot clinical trial is to evaluate the safety and tolerability of pirfenidone in patients with predicted moderately severe and severe acute pancreatitis. Pirfenidone is currently approved by FDA for the treatment of idiopathic pulmonary fibrosis. Now, over 5 years of data has accumulated demonstrating safety of its use in humans. The investigators' preclinical data suggest that pirfenidone is very effective in reducing the severity of acute pancreatitis in animal models. Following are the objectives of the proposed clinical trial:
Primary Objective:
* To evaluate the safety and tolerability of pirfenidone, compared to placebo, in patients predicted to have moderately severe or severe AP. * To evaluate the efficacy of pirfenidone in reducing the laboratory markers of inflammation and improving patient reported outcome measures.
Secondary Objective:
\- To evaluate the efficacy of pirfenidone in reducing the severity of acute pancreatitis, as measured by well-defined endpoints.
Eligibility criteria
Qualifiers
Patients 18 - 85 years of age
amylase or lipase values, or both, that are greater than 3 times the upper limit of normal values
characteristic cross-sectional imaging
typical upper abdominal pain- acute onset of a persistent, severe, epigastric pain often radiating to the back
Disqualifiers
Age < 18 or > 85 years
Body weight > 200 kg
Presentation to the medical attention > 48 h after diagnosis of AP
Inability to recruit, randomize and start the allocated treatment within 48h of start of pain
Trial design
Treatments tested in this trial
- Pirfenidone Oral Tablet
- Placebo
Treatment groups
Sponsors and collaborators
University of Alabama at Birmingham
Lead sponsor
Mayo Clinic
Collaborator