Safety and Tolerability of Pirfenidone in Acute Pancreatitis

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-85
SponsorUniversity of Alabama at Birmingham

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

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators