Phase 2 Pancreatitis Trial, Recruiting NCT06729996 Sponsor: Mayo Clinic Condition: Pancreatitis
Back to Pancreatitis

Phase 2 Pancreatitis Trial, Recruiting

NCT06729996
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 18 and 80 years old at the time of joining
  • You have been diagnosed with recurrent acute pancreatitis or chronic pancreatitis, AND also have diabetes (confirmed by imaging, specific study criteria, blood tests, or current diabetes medication)
  • You are able to give written consent and commit to follow-up visits over time
  • You have had a stable eye exam within the past year, or your most recent eye exam was stable and you are willing to schedule one during the study (an exception applies if you were diagnosed with diabetes within the last 6 months)
  • Your HbA1c (a blood sugar control measurement) is between 6.5% and 10.5% at your first study visit
  • You are currently taking diabetes medications (such as metformin or insulin), or no diabetes medications at all — and you are willing to temporarily stop certain medications under close medical supervision if required by the study team
  • If you are taking a GLP-1 medication (such as Ozempic, Wegovy, or similar), you have been on a stable dose for at least 3 months, your weight has been stable, and you agree not to increase the dose during the study
  • You are willing to check your blood sugar and ketone levels using meters provided by the study

Who may not be able to join:

  • You have had an allergic or sensitivity reaction to pioglitazone or empagliflozin, or you take medications that could interact with these drugs (confirm with trial site)
  • You are already taking pioglitazone or empagliflozin at the time of your first study visit
  • You have been diagnosed with Type 1 Diabetes
  • You are currently pregnant or breastfeeding, or a pregnancy test at screening comes back positive
  • You have a history of a bleeding disorder (such as hemophilia or von Willebrand disease)
  • You have liver disease or significantly elevated liver enzyme levels without a known cause
  • You are currently receiving treatment for cancer that involves systemic (whole-body) therapy — minor skin cancer treatments done in a dermatologist's office are generally acceptable
  • You have osteoporosis that is not being actively treated, based on the doctor's judgment
  • You have had an inflammatory illness (such as a respiratory infection or a pancreatitis episode) within the 30 days before joining
  • You have a history of moderate-to-severe heart failure (classified as NYHA Class III or higher) (confirm with trial site)
  • Your kidneys are not working well enough (kidney filtration rate below 30 mL/min) (confirm with trial site)
  • You have taken part in another clinical trial within 30 days before your first study visit
  • You are currently dependent on alcohol, tobacco, or other substances, based on the doctor's judgment
  • You are currently following a ketogenic (very low-carbohydrate) diet
  • You have autoimmune pancreatitis, pancreatitis caused by a blockage, or have had pancreatic surgery (such as a Whipple procedure, full or partial pancreas removal)
  • You have any other condition the study doctor believes could put your safety at risk, such as certain types of anemia, fluid retention, or heart failure
  • You have had a serious diabetes-related emergency (diabetic ketoacidosis) or signs of poorly controlled diabetes in the past 6 months, or your ketone levels are too high at your first study visit

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Yogish Kudva, Mayo Clinic

Phone: 507-255-1455

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
29 May 2025
Est. completion
31 May 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Hemoglobin A1c (HbA1c); Area under curve (AUC) for glucose; AUC for C-peptide; AUC for Insulin; AUC for glucagon

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov