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Sponsored by: |
Axcan Pharma |
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Information provided by: | Axcan Pharma |
ClinicalTrials.gov Identifier: | NCT00513682 |
This protocol will enroll children aged 7 to 11 years old, suffering from Cystic Fibrosis and Pancreatic Insufficiency in order to demonstrate the safety of Ultrase MT20 as well as the efficacy of this product in the improvement of the fat absorption.
Condition | Intervention | Phase |
---|---|---|
Cystic Fibrosis Pancreatic Insufficiency |
Drug: ULTRASE MT20 |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Crossover Assignment, Safety/Efficacy Study |
Official Title: | Efficacy and Safety of ULTRASE MT20 in Improving the Coefficient of Fat Absorption (CFA%) in Children With Cystic Fibrosis (CF) and Pancreatic Insufficiency (PI) |
Enrollment: | 9 |
Study Start Date: | July 2007 |
Study Completion Date: | April 2008 |
Primary Completion Date: | March 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
Treatment phase: Experimental
During the treatment phase, the patient will eat a high fat diet and will take ULTRASE MT20 at a specific daily dose to treat his pancreatic insufficiency.
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Drug: ULTRASE MT20
A stabilized dose of ULTRASE MT20 in capsules will be dispensed with each meal and snack during all days of the treatment phase.
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This study will include 3 phases: the screening phase, the washout phase and the treatment phase.
Screening Phase: this phase will last fifteen (15) days and all patients will take ULTRASE MT20 during this period. During the last 4 days, patents will be stabilized on a high fat diet and with Ultrase MT20.
Washout Phase: this phase will last 6 to 7 days. The patient will continue the high-fat diet but WILL REFRAIN from taking ULTRASE MT20 or any other enzymes. A 72-hour stool collection will be performed and all food consumed by the patient will be recorded to assess the Coefficient of Fat Absorption (CFA%) and the Coefficient of Nitrogen Absorption (CNA%).
Treatment Phase: this phase will last 7 to 11 days. The patient will continue the high-fat diet and will take the 'Stabilized Dose' of ULTRASE MT20 established during screening. Another 72-hour stool collection will be performed and all food consumed by the patient will be recorded to assess the Coefficient of Fat Absorption (CFA%) and the Coefficient of Nitrogen Absorption CNA%).
Ages Eligible for Study: | 7 Years to 11 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Michigan | |
University of Michigan Health System Cystic Fibrosis Center | |
Ann Arbor, Michigan, United States, 48109-0212 | |
United States, Ohio | |
Cystic Fibrosis Center Rainbow Babies and Children's HospitalDivision | |
Cleveland, Ohio, United States, 44106 | |
United States, Pennsylvania | |
Pennsylvania State University And the Milton S. Hershey Medical Center | |
Hershey, Pennsylvania, United States, 17033 |
Principal Investigator: | Michael Konstan, MD | Rainbow Baby- University hospital of Cleveland |
Study Director: | Jean Spénard, Ph.D | Axcan Pharma Inc. |
Study ID Numbers: | UMT20CF07-01 |
Study First Received: | August 7, 2007 |
Last Updated: | April 9, 2008 |
ClinicalTrials.gov Identifier: | NCT00513682 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Cystic Fibrosis Pancreatic insufficiency Steatorrhea Children 7 to 11 years pancreatic enzyme |
Digestive System Diseases Genetic Diseases, Inborn Respiratory Tract Diseases Cystic Fibrosis Fibrosis Lung Diseases |
Infant, Newborn, Diseases Pancreatic Diseases Pancrelipase Steatorrhea Exocrine Pancreatic Insufficiency |
Fibrosis Gastrointestinal Agents Pancrelipase Pharmacologic Actions Digestive System Diseases Pathologic Processes Cystic Fibrosis |
Respiratory Tract Diseases Genetic Diseases, Inborn Lung Diseases Therapeutic Uses Pancreatic Diseases Infant, Newborn, Diseases Exocrine Pancreatic Insufficiency |