Study Of Effects Of Oral CREON Capsules In Adult Participants With Exocrine Pancreatic Insufficiency Not Due To Cystic Fibrosis, Chronic Pancreatitis, Pancreatectomy, Or Pancreatic Cancer

Exocrine Pancreatic Insufficiency (EPI) Clinical Trial

Official title:

A Phase 4 Open-Label Single-Arm Study To Evaluate The Use Of CREON In Subjects With EPI Due To Etiologies Other Than Cystic Fibrosis, Chronic Pancreatitis, Pancreatectomy, Or Pancreatic Cancer

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04315311
• Other study ID #: M16-112
• Status: Withdrawn
• Phase: Phase 4
• Start date: May 6, 2020
• Est. completion date: September 22, 2021

Study information

• Verified date: November 2021
• Source: AbbVie
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Exocrine pancreatic insufficiency (EPI) is a condition where the pancreas does not have enough pancreatic enzymes to break down food. Some symptoms of EPI are frequent gas/bloating, unexplained stomach pains, frequent diarrhea, and foul-smelling, greasy stools. The purpose of this study is to see how effective CREON is for treating symptoms of EPI due to causes other than cystic fibrosis (CF), chronic pancreatitis (CP), pancreatectomy (PY), or pancreatic cancer (PC). CREON (Pancrelipase) is an approved drug used to treat people who cannot digest food normally due to their pancreas not making enough enzymes. Adult participants with a diagnosis of EPI due to causes other than CF, CP, PY, or PC will be enrolled. Around 50 participants will be enrolled in approximately 20 sites in the United States. Participants will receive oral CREON capsules with each meal and snack beginning at Day 1 for 27 weeks. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the course of the study at a hospital or a clinic. Participants will need to be confined for 2 separate periods of 6 to 8 days each to measure Co-efficient of Fat Absorption (during screening and after enrollment). The effect of the treatment will be checked by medical assessments, blood and stool tests, checking for side effects and completing questionnaires.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: September 22, 2021
• Est. primary completion date: September 22, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of exocrine pancreatic insufficiency (EPI).
• Participants who are on pancreatic enzyme replacement therapy (PERT) at the time of consent must have a clinical diagnosis of EPI by their physician.

Exclusion Criteria:

• History of cystic fibrosis, chronic pancreatitis, pancreatectomy, pancreatic cancer, or fibrosing colonopathy.

Related Conditions & MeSH terms

• Cystic Fibrosis
• Exocrine Pancreatic Insufficiency
• Exocrine Pancreatic Insufficiency (EPI)
• Pancreatitis
• Pancreatitis, Chronic

Intervention

Drug:
• CREON
Capsule: Oral

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
AbbVie

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change In Coefficient Of Fat Absorption (CFA) From Baseline	CFA is calculated as 100*[fat intake - stool fat]/fat intake. Fat intake will be determined from fat content of food consumed on Days 3 to 5 in the confinement period. Stool fat will be determined from the fat content in the stool(s) collected between the two dye markers in the confinement period.	Week 1
Secondary	Change In Gastrointestinal (GI) Symptoms From Baseline	Change in GI symptoms is measured by AbbVie exocrine pancreatic insufficiency (EPI) symptom questionnaire. EPI symptom questionnaire is a 12-item patient-reported outcome (PRO) instrument that assesses EPI symptoms over the past 7 days.	Week 1
Secondary	Change In Stool Frequency From Baseline	Stool frequency per 24 hours will be recorded daily during the 2 confinement periods. The average stool frequency per 24 hours during confinement period 1 will be considered as baseline.	Week 1
Secondary	Change In Stool Consistency From Baseline	Stool consistency will be evaluated using the Bristol Stool Scale. The Bristol Stool chart is a medical aid designed to classify feces.	Week 1
Secondary	Change In Vitamin D From Baseline	Change from Baseline in vitamin D will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Vitamin E From Baseline	Change from Baseline in vitamin E will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Vitamin K From Baseline	Change from Baseline in vitamin K will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Vitamin A From Baseline	Change from Baseline in vitamin A will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Retinol-Binding Protein From Baseline	Change from Baseline in retinol-binding protein will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Albumin From Baseline	Change from Baseline in albumin will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Prealbumin From Baseline	Change from Baseline in prealbumin will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Transferrin From Baseline	Change from Baseline in transferrin will be assessed through clinical laboratory testing.	Up To Week 27
Secondary	Change In Weight From Baseline	The mean change of weight from Baseline will be calculated.	Up To Week 27
Secondary	Change In Body Mass Index (BMI) From Baseline	BMI is a measure of body fat based on weight in relation to height.	Up To Week 27
Secondary	Change In Hip Circumference From Baseline	Hip circumference is measured by placing the measuring tape around the maximum circumference of the buttocks.	Up To Week 27
Secondary	Change In Waist Circumference From Baseline	Waist circumference is measured by placing a measuring tape on top of the hip bone and wrapping the tape around the waist.	Up To Week 27
Secondary	Change In Gastrointestinal Quality Of Life Index (GIQLI) From Baseline	GIQLI is a 36-item patient reported outcome (PRO) instrument used to assess GI-specific quality of life in participants with GI disorders, with response score ranging from 0 to 4 (0 being "all the time" and 4 being "never").	Up To Week 27

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