Efficacy and Safety of Ultrase® MT20 in Improving the Coefficient of Fat Absorption (CFA) in Children With Cystic Fibrosis (CF) and Pancreatic Insufficiency (PI)

PHASE3CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

July 31, 2007

Primary Completion Date

March 31, 2008

Study Completion Date

April 30, 2008

Conditions
Cystic FibrosisPancreatic Insufficiency
Interventions
DRUG

Ultrase® MT20

Ultrase® MT20 capsules will be administered orally with each meal during Day 1 to 15 in screening phase at a dose based on investigator's discretion. During Day 12 to 15, participants will receive high-fat diet and Ultrase® MT20 dose will be adjusted depending on symptoms of steatorrhea. This will be followed by a washout phase of 6 to 7 days, in which participants will receive only high-fat diet; then stabilized dose of Ultrase® MT20 capsule (as identified during screening phase) will be administered orally for 7 to 11 days during treatment phase. The stabilized dose should not to exceed 2500 lipase units per kilogram body weight per meal (lipase units/kg/meal).

Trial Locations (3)

17033

Pennsylvania State University And the Milton S. Hershey Medical Center, Hershey

44106

Cystic Fibrosis Center Rainbow Babies and Children's HospitalDivision, Cleveland

48109-0212

University of Michigan Health System Cystic Fibrosis Center, Ann Arbor

Sponsors
All Listed Sponsors
lead

Forest Laboratories

INDUSTRY