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Study Investigating a Delayed-Release Pancrelipase in Patients With Exocrine Pancreatic Insufficiency Due to Cystic Fibrosis

Phase 3
Completed
Conditions
Cystic Fibrosis
Interventions
Drug: Pancrelipase Delayed Release
Drug: Placebo Comparator
Registration Number
NCT00510484
Lead Sponsor
Solvay Pharmaceuticals
Brief Summary

This study will assess the effect of pancrelipase delayed release 24,000 unit capsules on fat and nitrogen absorption in subjects with PEI due to Cystic Fibrosis.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
35
Inclusion Criteria
  • Confirmed CF diagnosis by two positive chloride sweat tests or gene analysis
  • Confirmed PEI by historical CFA < 70% without supplementation or current or historical fecal elastase < 50ยตg/g stool (within the last 12 months)
  • Subjects of 12 years or older
  • Currently receiving treatment with a commercially available pancreatic enzyme product on a stable dose for more than 3 months
  • Clinically stable condition without evidence of acute respiratory disease or any other acute condition
  • Females of child-bearing potential must agree to continue using a medically acceptable method of birth control
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Exclusion Criteria
  • Ileus or acute abdomen
  • History of fibrosing colonopathy
  • History of distal ileal obstruction syndrome within 6 months of enrollment
  • Use of an immunosuppressive drug
  • Any type of malignancy involving the digestive tract in the last 5 years
  • Known infection with HIV
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
APancrelipase Delayed Release-
BPlacebo Comparator-
Primary Outcome Measures
NameTimeMethod
Coefficient of Fat Absorption (%)5 days

This coefficient is calculated from fat intake and fat excretion : 100\*\[fat intake-fat excretion\]/fat intake. Stools were collected on 3 days during the 5 days treatment period. Higher values indicate a better response.

Secondary Outcome Measures
NameTimeMethod
Coefficient of Nitrogen Absorption (%)5 days

This coefficient is calculated from nitrogen intake and nitrogen excretion : 100\*\[nitrogen intake-nitrogen excretion\]/nitrogen intake. Stools were collected on 3 days during the 5 days treatment period. Higher values indicate a better response.

Total Fat Excretion (Grams)5 days

Total amount of fat excreted during the stool collection period. Stools were collected on 3 days during the 5 days treatment period. Lower values indicate a better response.

Total Stool Weight (Grams)5 days

Total weight of the stools collected during the stool collection period. Stools were collected on 3 days during the 5 days treatment period. Lower values indicate a better response.

Stool Frequency5 days

Stool frequency is the average of the daily number of stools recorded during the treatment period. Lower values indicate a better response.

Percentage of Days With no Flatulence.5 days

The percentage of days with no flatulence is calculated from the diary during the treatment period: 100\*(number of days with no flatulence/number of days recorded in diary). Higher values indicate a better response.

Percentage of Days With no Abdominal Pain.5 days

The percentage of days with no abdominal pain is calculated from the diary during the treatment period: 100\*(number of days with no abdominal pain / number of days recorded in diary). Higher values indicate a better response.

Trial Locations

Locations (23)

Site 20

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Petrofi, Hungary

Site 7

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Louisville, Kentucky, United States

Site 12

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Dayton, Ohio, United States

Site 22

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Johannesburg, South Africa

Site 2

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Toledo, Ohio, United States

Site 3

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Hershey, Pennsylvania, United States

Site 10

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Los Angeles, California, United States

Site 13

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San Francisco, California, United States

Site 17

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Boston, Massachusetts, United States

Site 6

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Minneapolis, Minnesota, United States

Site 19

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Cincinnati, Ohio, United States

Site 14

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Oklahoma City, Oklahoma, United States

Site 15

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Philadelphia, Pennsylvania, United States

Site 9

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Nashville, Tennessee, United States

Site 4

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Orlando, Florida, United States

Site 5

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Miami, Florida, United States

Site 1

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Iowa City, Iowa, United States

Site 18

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Long Branch, New Jersey, United States

Site 8

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Ann Arbor, Michigan, United States

Site 23

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Barcelona, Spain

Site 11

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Long Beach, California, United States

Site 16

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Albuquerque, New Mexico, United States

Site 21

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Jerusalem, Israel

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