Control of Steatorrhea in Participants With Cystic Fibrosis and Exocrine Pancreatic Insufficiency

Forest Laboratories

Status and phase

Completed

Phase 4

Conditions

Cystic Fibrosis

Exocrine Pancreatic Insufficiency

Treatments

Drug: Kreon® 25,000

Drug: Panzytrat® 25,000

Study type

Interventional

Funder types

Industry

Identifiers

NCT01327703

2010-019267-11 (EudraCT Number)

MA-PA25CF10-01

Details and patient eligibility

About

This study by Aptalis (formerly Axcan) assesses the efficacy and safety of Panzytrat® 25,000 compared to Kreon® 25,000 in the control of steatorrhea in participants with cystic fibrosis (CF) and exocrine pancreatic insufficiency (EPI).

Full description

This is an open-label, Phase IV, multicenter, randomized, two-period cross-over study to compare the efficacy and safety of Panzytrat® 25,000 to Kreon® 25,000 in participants aged 7 years and older suffering from CF and EPI. The study consists of a qualification phase (5 to 15 days); two treatment periods of 14 days each (plus a 3-day window if needed) and a 3-day stool collection will be performed from Days 12 to 15.

A safety follow-up phone call will be arranged 7-10 days after completion of the treatment phase or after an early discontinuation.

Enrollment

87 patients

Sex

All

Ages

7+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Participant or his/her legal representative signed informed consent form (ICF) prior to starting any study procedures
Participant with clinical diagnosis of CF based on one or more typical clinical features of CF phenotype, in addition to one of the following: a genotype that documents the presence of 2 CF-causing mutation, or a sweat chloride test greater than or equal to 60 millimole per liter (mmol/L) by quantitative pilocarpine iontophoresis on two separate occasions
Participant with severe EPI confirmed by enzyme-linked immunosorbent assay (ELISA) measurement of fecal elastase-1 (FE-1)
Male or female participant aged 7 years or older
Participant currently receiving and has received a stable dose of lipase with either Panzytrat® 25,000 or Kreon® 25,000 for at least 30 days prior to ICF signature
Participant generally in good health, except for the underlying symptoms associated with CF and EPI, and is clinically stable (no change in the last 30 days of physical examination) as evidenced by medical and medication histories, physical examination including vital signs during screening and laboratory tests
Participant able to maintain a CF standardized diet with a lipid content customized to his/her needs during the study according to the qualification phase diary
Women of childbearing potential must have a negative pregnancy test at study entry and must use a medically acceptable contraceptive method for the duration of the study

Exclusion criteria

Participant with known contraindication, sensitivity or hypersensitivity to Panzytrat® 25,000 or Kreon® 25,000, or to any porcine protein
Participant who recently received treatment of an emergent acute infection with oral or intravenous (IV) antibiotics that was not stopped at least 14 days prior to randomization
Participant with chronic use of narcotics that were not stopped at least 7 days prior to the qualification visit
Participant using of any prohibited medications or products listed in the prohibited medication section of the protocol
Participant with acute pancreatitis or exacerbation of chronic pancreatic disease
Participant with history of significant bowel resection that could impair fat absorption
Participant with any condition known to increase fecal fat loss including but not limited to: celiac disease, Crohn's disease, tropical sprue, bacterial bowel infection, liver disease, lactose intolerance, pseudomembranous colitis, biliary and pancreatic cancer, radiation enteritis, Whipple's disease, Whipple's procedure, etc
Participant with any significant gastrointestinal dysmotility disorders
Participant with chronic abdominal pain or severe abdominal pain at study entry
Participant using enteral tube feeding over day and night
Participant with history or presence of clinically significant portal hypertension
Participant with history or presence of complete distal intestinal obstruction syndrome (DIOS) in the past 6 months, or 2 or more episodes of DIOS in the past year
Participant with poorly controlled diabetes as per the investigator's opinion
Female participants who are pregnant or breastfeeding
Participant with any condition or history of any illness, or pre-study laboratory abnormality which, in the opinion of the investigator or sponsor, might put the participant at risk, prevent the participant from completing the study, or otherwise affect the outcome of the study
Participant using any investigational drug within 30 days prior to the date of signature of the ICF