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Recurrent Acute PancreatitisPhase 2PirfenidoneRAPNCT06253117

Evaluation of Pirfenidone as a Novel Therapeutic Strategy Against Recurrent Acute Pancreatitis.

A Phase 2 study testing Pirfenidone in people with Recurrent Acute Pancreatitis, run by University of Alabama at Birmingham at 3 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This clinical will evaluate the safety, tolerability and early efficacy of pirenidone in patients with recurrent acute pancreatitis. Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Recurrent Acute Pancreatitis
What is being tested?
Pirfenidone
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
60 participants
Where
3 sitesUnited States
Study dates
27 Jun 2024to 1 Sep 2028
Phase
Phase 2
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

A- Inclusion Criteria:

  1. Patients 18 - 85 years of age
  2. Two or more documented attacks of acute pancreatitis, separated by 3 months from one another, defined by at least 2 of the following 3:
  3. amylase or lipase values, or both, that are greater than 3 times the upper limit of normal values
  4. characteristic cross-sectional imaging
  5. typical upper abdominal pain according to the revised Atlanta classification28
  6. Drug/placebo treatment to start
  7. Mild AP Patient is discharged out of the hospital 30 days after diagnosis of mild AP
  8. Moderate Severe or Severe AP Patient is discharged out of hospital Intra-abdominal collections are either resolved on imaging, or are improving and asymptomatic (VAS Pain score ≤3 [with or without pain medication], vomiting ≤once a week, tolerating light diet, and no fever and chills) and do not warrant any intervention (per treating physician)
  9. Ability to understand and the willingness to sign a written informed consent document and medical release
  10. Willing and able to comply with trial protocol and follow up
  11. 2nd AP episode despite correction of the AP etiology (if identified) after the 1st episode as follows i. Patients with biliary pancreatitis who have undergone cholecystectomy, with or without ERCP (if indicated) ii. Patients with hypertriglyceridemia induced pancreatitis who have serum triglyceride levels below 400 while on medication management iii. Patients with medication induced AP developing a 2nd AP episode despite stopping the culprit medication

B- Exclusion Criteria:

  1. Age < 18 or > 85 years.
  2. Body weight > 200 kg.
  3. Ongoing AP (in right clinical situation defined by pain>3, vomiting ≥once a week, fever or chills, not tolerating light diet) or diagnosis of AP in previous 30 days.
  4. Diagnosis of chronic pancreatitis, one of the following
  5. Ductal stricture, calcification and/or atrophy, as seen on CT scan/MRI
  6. 5 or more of the 9 EUS criteria used to diagnose CP
  7. Known hypersensitivity to Pirfenidone.
  8. AST/ALT > 3 times the upper normal limit.
  9. Alkaline phosphatase >2.5 times the upper normal limit.
  10. Bilirubin higher than upper normal limit.
  11. Moderate to severe heart failure and/or coronary heart disease (New York Heart Association (NYHA) Functional Class III/IV).
  12. On home oxygen or home mechanical ventilation.
  13. Advanced liver disease as defined by Child-Pugh cirrhosis B or C.
  14. Paralytic ileus or significant nausea and vomiting preventing administration of light diet.
  15. Chronic diarrhea (>6 months, 3 or more stools/day-Clinically not appearing to be steatorrhea [fecal fat if done less than 15 g per day and fecal elastase if done more than 100].Active cancer (on chemotherapy, radiation or treatment of cancer at the time of enrollment) or cancer free <3 years (non-melanoma skin cancer are not a contraindication)
  16. Known cancer that is end-stage with ongoing palliative care or for which palliative care is appropriate.
  17. Known history of infective hepatitis (Hepatitis B or C)[can enroll if treatment and cure is documented]
  18. Ongoing photosensitivity and rash.
  19. Known live vaccines or therapeutic infectious agents within one month of admission.
  20. Known pregnancy or lactation at the time of admission.
  21. Women of childbearing potential who are not on oral or injectable contraceptives or IUDs, and do not consent to adequate contraception while on, and for 90 days after the administration of the drug/placebo.
  22. Known to be currently participating in a trial testing any investigational medicinal product or participation in a clinical study involving a medicinal product in the last three months.
  23. Problematic pattern of alcohol use or moderate to severe alcohol use disorder (Appendix 2)
  24. Substance use disorder (except recreational or medicinal use of marijuana) [if patient underwent and completed a rehab program, has not used substances for at least one year, and has an adequate support system, they may be enrolled]
  25. Family or personal history of long QT syndrome (> 500 msec).
  26. Strong CYP1A2 inhibitors (e.g., fluvoxamine, enoxacin) or moderate CYP1A2 Inhibitors (e.g., ciprofloxacin).
  27. Renal disease with GFR < 30.
  28. Any condition other than above that, in the opinion of the investigator, is likely to result in the death of the patient within the next 2 years.
  29. Any condition that, in the opinion of the investigator, might be significantly exacerbated by the known side effects associated with the administration of Pirfenidone.

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Kondal Kyanam, M.B.B.S. contact

(205) 975-3593

kbaig@uabmc.edu

Santhi Swaroop Vege, M.D. contact

United States3 sites, 3 recruiting
  • University of Alabama at Birmingham

    Birmingham, Alabama, 35294

    kondal kyanam, MD, (205) 975-3593, kbaig@uabmc.edu

    Recruiting
  • University of Iowa Health Care

    Iowa City, Iowa, 52242

    Rimas Rimas Nemickas, 319-353-8863, rimas-nemickas@uiowa.edu

    Vikas Dudeja, MBBS, FACS

    Recruiting
  • Mayo Clinic

    Rochester, Minnesota, 55905

    Santhi S Vege, 1-507-284-2511, OspinaVelasquez.Luis@mayo.edu

    Recruiting

Other trials in United States

About this study

This clinical will evaluate the safety, tolerability and early efficacy of pirenidone in patients with recurrent acute pancreatitis.

Read the detailed description

Background: Recurrent Acute Pancreatitis (RAP) is occurrence of 2 or more distinct episodes of Acute Pancreatitis (AP) (separated by at least 3 months). RAP not only leads to significant morbidity and reduced quality of life; patients with RAP have a substantial (up to 40%) risk of progressing to chronic pancreatitis (CP). Unfortunately, there is no therapy, which can help prevent future attacks of pancreatitis in RAP patients. In this regard, our published work suggest that pirfenidone, a therapy approved by FDA for the treatment of Idiopathic Pulmonary Fibrosis (IPF), has the potential to emerge as a novel treatment for patients with RAP. Briefly, our results suggest that: 1) Pirfenidone, when administered prophylactically, reduces the risk of AP development; 2) Pirfenidone, when given to experimental animals with severe AP, leads to amelioration of local and systemic injury; and 3) Pirfenidone, when administered to experimental animals with ongoing RAP, reduces risk of progression to CP. Thus, our results suggest that pirfenidone has potential to emerge as novel therapeutic strategy for RAP patients. These studies have high translational value as pirfenidone is already in clinical use for IPF and has over 8 years of record of safety.

Hypothesis: "Pirfenidone treatment in patients with RAP will be safe, tolerable, and efficacious." Objectives: The study has following primary and secondary objectives. Primary Objective: 1) To evaluate the safety and tolerability of pirfenidone compared to placebo, in patients with RAP. 2) To evaluate the efficacy of pirfenidone in reducing the laboratory markers of inflammation.

Secondary Objective: 1) To evaluate the efficacy of pirfenidone in reducing- a) recurrence of AP; b) pancreatitis related emergency room visits and readmissions; c) severity of pancreatitis, if acute pancreatitis was to develop; d) Improving quality of life measures; e) Improvement in patient reported outcomes. 2) To develop a predictive biomarker of efficacy of pirfenidone, which can be incorporated in a future clinical trial.

Specific aims and study design. Pilot Clinical Trial of the Safety, Tolerability and Efficacy of Pirfenidone in RAP. We will conduct a randomized, double-blind, placebo controlled pilot trial of pirfenidone in patients with RAP. RAP patients, 18-85 years of age who meet the eligibility criteria, will be recruited at one of the three participating sites (UAB, Mayo clinic Rochester and Brigham and Women's Hospital, Boston), and randomly assigned to pirfenidone or placebo treatment for 6 months. The primary endpoints of this clinical trial are a) feasibility; and b) safety. We have multiple efficacy secondary endpoints endpoint like cumulative incidence and rate of recurrent attacks of AP, severity of recurrent attacks of AP (mild/moderate/severe), readmissions and/or ER visits for pain, changes in quality of life as measured by PANQOLI and SF-12 health survey questionnaires, and changes in changes in patient reported outcome as measured by PAN-PROMISE score. We plan to recruit 60 patients at the three study sites over the duration of this clinical trial.

Being tested
Pirfenidone, Placebo
Medical subject headings
Pancreatitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PirfenidoneDrug

    Pirfenidone Days 1-7: 267 mg PO TID (801 mg/day) Days 8-14: 534 mg PO TID (1602 mg/day) Day 15 and thereafter: 801 mg PO TID; not to exceed 2403 mg/day

    Duration of treatment- total 6 months

  • PlaceboDrug

    Placebo

Study groups in NCT06253117
Study groupRoleWhat they receive
PlaceboPlacebo comparatorPlacebo
Receives: Drug: Placebo
PirfenidoneExperimentalPirfenidone Days 1-7: 267 mg PO TID (801 mg/day) Days 8-14: 534 mg PO TID (1602 mg/day) Day 15 and thereafter: 801 mg PO TID; not to exceed 2403 mg/day Total duration of experimental or placebo drug treatment 6 months
Receives: Drug: Pirfenidone

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Adverse Event

    Development of anticipated or un-anticipated serious adverse events (class 3-4)

    Measured: 6 months

Secondary outcomes (15)
  1. Development of Recurrent AP

    Cumulative incidence and rate of recurrent attacks of AP over 2 year period following randomization into drug/placebo

    Measured: 2 years

  2. Severity of Recurrent Attacks of AP

    Classified as mild/moderate/severe

    Measured: 2 years

  3. ER Visits

    Readmissions and/or ER visits for pain but not AP, over 2 years following randomization into drug/placebo

    Measured: 2 years

  4. QOL

    SF-12 (0-100, higher score means better physical and mental health functioning)

    Measured: 2 years

  5. Patient reported outcomes

    Changes in patient reported outcome as measured by PAN-PROMISE score (0-70, with higher score meaning worse symptoms)

    Measured: 2 years

  6. Laboratory Marker of Inflammation

    Changes in the laboratory markers of inflammation CRP

    Measured: 2 years

  7. Laboratory Marker of Inflammation

    Changes in the laboratory markers of inflammation IL-10

    Measured: 2 years

  8. Laboratory Marker of Inflammation

    Changes in the laboratory markers of inflammation TNF-α

    Measured: 2 years

  9. Laboratory Marker of Inflammation

    Changes in the laboratory markers of inflammation IL-1

    Measured: 2 years

  10. Laboratory Marker of Inflammation

    Changes in the laboratory markers of inflammation IL-6

    Measured: 2 years

  11. Laboratory Marker of Inflammation

    Changes in the laboratory markers of inflammation Angiopoietin-2

    Measured: 2 years

  12. Development of CP

    Fecal Elastase

    Measured: 2 years

  13. Development of Chronic Pancreatitis

    Development of CP, as evaluated by secretin MRCP at the end of the study

    Measured: 2 years

  14. Development of Diabetes

    hemoglobin A1C

    Measured: 2 years

  15. Development of Diabetes

    Fasting blood sugar

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Feb 2024
  2. Study start27 Jun 2024
  3. Primary completion1 Sep 2028 (estimated)
  4. Study completion1 Sep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06253117
Sponsor's protocol ID
IRB-300012263
Other IDs
HT9425-23-1-0900
Acronym
PirfenidoneRAP
Status last verified
Jul 2026
First submitted
20 Jan 2024
Last updated
29 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Publications

  • Jain T, Iyer S, Bava EP, Kannan AB, Bhandari S, Suryansh S, Ospina Velasquez LE, Gage H, Himle B, Al-Obaidi M, Evans Z, Kulkarni T, Ashat M, Abbasi A, Hashimoto R, Phillips AE, Jayaram NB, Yadav D, Kyanam Kabir Baig KR, Vege SS, Dudeja V. Evaluation of Pirfenidone for Recurrent Acute Pancreatitis: Protocol for a Randomized Trial. J Surg Res. 2026 Oct 22;328:185-192. doi: 10.1016/j.jss.2026.09.023. Online ahead of print.

    PubMed 42913268

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Pirfenidone in people with Recurrent Acute Pancreatitis, run by University of Alabama at Birmingham at 3 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 29 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Kondal Kyanam, M.B.B.S. ((205) 975-3593, kbaig@uabmc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Adverse Event (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06253117, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Jul 2026.

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