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RecruitingNCT07852988Updated Oct 1, 2026

Pancreatin Added to Standard Antihyperglycemic Therapy in Patients With Type 2 Diabetes

A Phase 4 interventional study of Pancreatin and Placebo in Type 2 Diabetes (T2DM), sponsored by Silesian Centre for Heart Diseases. Recruiting at 1 site in Poland. Open to participants aged 35 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-10-01.

Sponsored by Silesian Centre for Heart Diseases · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Updated Oct 1, 2026Newly registeredGo to Updates ↓
Phase
Phase 4
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
35 Years to 75 Years
Sex
All
01

Study summary

Medications that enhance the incretin effect (GLP-1 receptor agonists, tirzepatide (GIP/GLP-1 receptor agonist) and DPP-4 inhibitors) are used in treatment of patients with type 2 diabetes. GLP-1 agonists and tirzepatide not only effectively lower blood glucose levels but also promote weight loss-primarily by stimulating the satiety center in the central nervous system - and reduce cardiovascular risk. Evidence suggests that oral pancreatin supplementation also enhances the incretin effect by increasing GIP and GLP-1 concentrations, and consequently insulin levels, which translates into a reduction in postprandial glycemia in patients with cystic fibrosis or chronic pancreatitis. In our study we aim to evaluate the impact of pancreatin on the incretin effect and glycemic control in patients with type 2 diabetes without exocrine pancreatic insufficiency.

Read the detailed description

Glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are the two primary incretin hormones secreted from the small intestine on ingestion of glucose or nutrients to stimulate insulin secretion from pancreatic β cells. They play a role in regulation of blood glucose levels, particularly postprandial glycemia. Lipids and carbohydrates are the most potent stimulators of incretin hormone secretion. Pancreatin is a mixture of digestive enzymes naturally produced by the pancreas, which is used as a medication supporting macronutrient digestion, especially in cases of exocrine pancreatic insufficiency. Evidence suggests that oral pancreatin supplementation enhances the incretin effect by increasing GIP and GLP-1 concentrations, and consequently insulin levels, which translates into a reduction in postprandial glycemia in patients with cystic fibrosis or chronic pancreatitis. Based on a randomized, placebo-controlled, double-blind study, we aim to evaluate the effect of pancreatin on the incretin effect and glycemic control in patients with type 2 diabetes without exocrine pancreatic insufficiency.

We plan to recruit a total of 100 patients with type 2 diabetes treated with oral antihyperglycemic drugs or insulin, either as monotherapy or in combination. Patients will be randomly divided into 2 groups:

  • Group of 50 patients receiving pancreatin 25 000 U with up to 3 main meals daily for 3 months
  • Group of 50 patients receiving placebo with up to 3 main meals daily for 3 months

Baseline assessment:

  • Anthropometric parameters: body weight, height, waist-to-hip ratio, body composition (bioelectrical impedance analysis)
  • Laboratory tests: aspartate aminotransferase, alanine aminotransferase, serum amylase, lipid profile, HbA1c, selected cytokines, average glucose concentration from the last 7 days before study start (glucometer - 4 measurements per day), data from the FreeStyle Libre2 continuous glucose monitoring system (2 weeks prior to study start): assessment of TIR (Time in Range 70-180 mg/dL), glycemic variability coefficient (CV), standard deviation (SD), mean glucose concentration, frequency and severity of hypoglycemia; daily insulin requirements from the last 7 days (for insulin-treated patients)

Assessment after study completion:

  • Anthropometric parameters: body weight, height, waist-to-hip ratio, body composition (bioelectrical impedance analysis)
  • Laboratory tests: aspartate aminotransferase, alanine aminotransferase, serum amylase, lipid profile, HbA1c, selected cytokines, average glucose concentration from the last 7 days before study end (glucometer - 4 measurements per day), data from the FreeStyle Libre 2 continuous glucose monitoring system (last 2 weeks of study): assessment of TIR, CV, SD, mean glucose concentration, frequency and severity of hypoglycemia; daily insulin requirements from the last 7 days (for insulin-treated patients).

Should pancreatin demonstrate a beneficial effect on glycemic homeostasis, these formulations could serve as a valuable adjunctive therapy for type 2 diabetes.

02

Conditions studied

  • Type 2 Diabetes (T2DM)

Keywords

  • type 2 diabetes
  • pancreatin
  • glycemic control
  • incretin effect
03

In context

Diabetes Mellitus, Type 2

9,357 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,318 are open to participants now.

This study's planned enrollment of 100 is above the median of 80 across 7,523 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

Silesian Centre for Heart Diseases is the lead sponsor of 17 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Type 2 diabetes diagnosed for at least 12 months
  • Patients treated with oral antihyperglycemic agents and/or insulin as monotherapy or combination therapy
  • Age between 35 and 75 years
  • HbA1c: 6.5% - 9.0%

Exclusion criteria

Exclusion Criteria:

  • Type 1 diabetes
  • Use of incretin-based drugs (GLP-1 receptor agonists, dual GIP and GLP-1 receptor agonists, DPP-4 inhibitors) currently or within the last 3 months
  • History of pancreatic surgery
  • History of chronic pancreatitis
  • History of acute pancreatitis
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Pancreatin

    Participants receiving pancreatin

    Drug: Pancreatin

  • Placebo comparator
    Control

    Participants receiving placebo

    Drug: Placebo

Interventions

  • DrugPancreatin

    Pancreatin 25 000 U with each of the 3 main meals daily for 3 months

    Also known as: ActiveLab

  • DrugPlacebo

    Placebo capsule with each of the 3 main meals daily for 3 months

    Also known as: ActivLab Placebo

06

What researchers measure

Primary outcomes

  1. Glycemic control

    HbA1c value

    Time frame: 3 months

  2. Time in range

    Time in range (glucose 70-180 mg/dl)

    Time frame: 3 months

Secondary outcomes

  1. Body weight

    Body weight measurement

    Time frame: 3 months

  2. Lipid profile

    Total cholesterol, LDL-cholesterol, HDL-cholesterol, Triglicerides

    Time frame: 3 months

07

Study locations

1 of 1 sites recruiting
  • Department of Internal Medicine, Diabetology and Cardiometabolic Disorders, Faculty of Medical Sciences Zabrze
    Zabrze, Silesian Voivodeship 41-800, Poland
    Recruiting
08

References and documents

Publications

  • Perano SJ, Couper JJ, Horowitz M, Martin AJ, Kritas S, Sullivan T, Rayner CK. Pancreatic enzyme supplementation improves the incretin hormone response and attenuates postprandial glycemia in adolescents with cystic fibrosis: a randomized crossover trial. J Clin Endocrinol Metab. 2014 Jul;99(7):2486-93. doi: 10.1210/jc.2013-4417. Epub 2014 Mar 26. PubMed 24670086 ↗
  • Knop FK, Vilsboll T, Larsen S, Hojberg PV, Volund A, Madsbad S, Holst JJ, Krarup T. Increased postprandial responses of GLP-1 and GIP in patients with chronic pancreatitis and steatorrhea following pancreatic enzyme substitution. Am J Physiol Endocrinol Metab. 2007 Jan;292(1):E324-30. doi: 10.1152/ajpendo.00059.2006. Epub 2006 Sep 5. PubMed 16954337 ↗
  • Ebert R, Creutzfeldt W. Reversal of impaired GIP and insulin secretion in patients with pancreatogenic steatorrhea following enzyme substitution. Diabetologia. 1980 Sep;19(3):198-204. doi: 10.1007/BF00275269. PubMed 6997121 ↗

Individual participant data

Plan to share: Yes — Deidentified individual participant data and the study protocol will be made available upon reasonable request.

Supporting information: Study protocol, Sap, Icf

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 1, 2026
Show all 1 update
  1. Oct 1, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07852988
Lead sponsor
Silesian Centre for Heart Diseases
Collaborators
Medical University of Silesia
Responsible party
Sponsor
First posted
Oct 1, 2026
Start date
Aug 1, 2026
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Oct 1, 2026

Study contacts

Marta Wróbel, PhD
Contact
mwrobel@sum.edu.pl
48606873060
Paulina Piekarz-Ząbek, MD
Contact
k_bielawa@poczta.fm
‭+48 604 223 652‬
Marta Wróbel, PhD
principal investigator · Department of Internal Medicine, Diabetology and Cardiometabolic Disorders

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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