Study to Evaluate the Safety and Efficacy of EUR-1008 (APT-1008) Pancreatic Enzyme Product in Participants With Cystic Fibrosis and Exocrine Pancreatic Insufficiency

NCT00297167 | Completed Phase 3 Results

• 1 other identifier: EUR-1008-M
• Study Type: interventional
• Target: 34
• Locations: 1 country
• Sites: 1

Brief Summary

The primary efficacy objective of this study is to compare the coefficient of fat absorption (CFA) following oral administration of Aptalis Pharma's (formerly Eurand Pharmaceuticals) pancreatic enzyme product (PEP) capsules and placebo in participants with cystic fibrosis (CF) and exocrine pancreatic insufficiency (EPI).

Conditions

Cystic Fibrosis; Exocrine Pancreatic Insufficiency

Keywords

CF; Cystic Fibrosis; EPI; Exocrine Pancreatic Insufficiency; Pancreatic; Enzyme; PEP

Outcome Measures

Primary Outcomes (1)

• Percent Coefficient of Fat Absorption (CFA%)

  Percent CFA was calculated as (\[fat intake - fat excretion\]/fat intake)multiplied by 100, determined in the stools collected during the 72-hour hospitalization period. Mean percent CFA was calculated for Day 3 to Day 6 during hospital treatment in first and second double-blind (DB) intervention periods.

  Day 3 up to Day 6 of hospital treatment in first and second double-blind intervention periods

Secondary Outcomes (7)

• Percent Coefficient of Nitrogen Absorption (CNA%)

  Day 3 up to Day 6 of hospital treatment in first and second double-blind intervention periods

• Lipid Levels

  End of treatment (Day 6 during first and second double-blind intervention periods)

• Vitamin A Levels

  End of treatment (Day 6 during first and second double-blind intervention periods)

• Vitamin E Levels

  End of treatment (Day 6 during first and second double-blind intervention periods)

• Mean Daily Number of Stools

  Day 3 up to Day 6 during first and second double-blind intervention periods

Other Outcomes (2)

• Percentage of Visible Oil or Grease in Stool

  Day 3 up to Day 6 of hospital treatment in first and second double-blind intervention periods

• Percentage of Stools With Blood

  Day 3 up to Day 6 of hospital treatment in first and second double-blind intervention periods

Study Arms (2)

EUR-1008 (APT-1008) First, Then Placebo

EXPERIMENTAL

Drug: EUR-1008 (APT-1008); Drug: Placebo

Placebo First, Then EUR-1008 (APT-1008)

EXPERIMENTAL

Drug: Placebo; Drug: EUR-1008 (APT-1008)

Interventions

EUR-1008 (APT-1008) DRUG

EUR-1008 (APT-1008) microtablets (5000 lipase units) or minitablets (10000, 15000 or 20000 lipase units) contained in a capsule will be given orally daily in first double-blind intervention period; at a dose based on investigator's discretion as achieved during dose titration and stabilization period (6 to 9 days). The capsules could be opened and sprinkled on acidic food and half of the established dose was used with snacks. Treatment duration for first double-blind intervention period will be 2 days home treatment and 3 to 5 days hospital treatment.

EUR-1008 (APT-1008) First, Then Placebo

Placebo DRUG

Placebo matched to EUR-1008 (APT-1008) microtablets or minitablets contained in a capsule will be given orally daily in second double-blind intervention period; at a dose based on investigator's discretion as achieved during dose titration and stabilization period (6 to 9 days). Treatment duration for second double-blind intervention period will be 2 days home treatment and 3 to 5 days hospital treatment.

EUR-1008 (APT-1008) First, Then Placebo

Eligibility Criteria

• Age: 7 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Participants with age greater than or equal to (\>=) 7 years at the time of enrollment
• Participants with weight 70 kg or less and be in an adequate nutritional status as indicated by a body mass index (BMI) \>=20 kg/m\^2 for ages 18 and above, or a BMI above the twenty fifth percentile for participants aged 7 to 17 years
• Participants with confirmed diagnosis of CF who have 2 clinical features consistent with CF, and have either a genotype with 2 identifiable mutations consistent with CF or a sweat chloride concentration that is more than 60 milliequivalent per liter by quantitative pilocarpine iontophoresis
• Participants with confirmed diagnosis of EPI who are currently receiving treatment with a commercially available PEP and have documented with a fecal elastase of \<100 microgram per gram stool (if no documentation was available, a stool sample was taken at Screening for determination of fecal elastase).
• Clinically stable participants with no evidence of acute respiratory disease or any other acute condition
• Participants who are willing and able to interrupt current CF treatment for CF-related malabsorption along with any medications that may affect gastric motility or stomach power of hydrogen (pH)
• Participants 18 years of age and older had to a) understand the requirements of the study, b) provide written informed consent, c) agree to abide by the study restrictions, and d) return for the required assessments
• Participants 7 to 17 years of age must have a parent(s) or legal guardian who provides written informed consent, agree to abide by the study restrictions
• Females participants of childbearing potential must have a negative serum pregnancy test at screening and must agree to use adequate birth control during the study

You may not qualify if:

• Participants with fibrosing colonopathy, hyperuricemia or hyperuricosuria
• Participants who are allergic to pork or other porcine PEPs
• Participants with forced expiratory volume (FEV1) \<30 percent of predicted FEV1 at screening
• Participants with any acute systemic administration of an antibiotic for any reason in the previous 4 weeks; however, a low stable dose of an antibiotic or chronic treatment with an inhalatory antibiotic is allowed
• Participants with hepatic insufficiency as defined by history or presence of ascites or serum albumin level of \< 3.0 milligram/deciliter, or a coagulopathy with an international normalized ratio that is greater than 1.7
• Participants who have used an acute dose of any steroid in the previous 2 weeks; however, low chronic doses of a steroid is allowed
• Participants with history of or current diagnosis of distal ileal obstruction syndrome (DIOS) as evidenced or suggested by constipation, abdominal pain, anorexia, early satiety, recurrent vomiting, and palpable fecal mass on physical examination (the absence of DIOS will be confirmed by an X-ray of the abdomen taken at screening)
• Participants with any solid organ transplant or surgery affecting the bowel. Participants with a history of appendectomy and inguinal (non-incarcerated) hernioplasty or meconium ileus without the need for bowel resection could be enrolled. Gastrointestinal-tube-fed patients, in absence of dumping syndrome, were also eligible
• Participants with history of or current screening evaluation of hyperglycemia as defined by an 8-hour fasting blood glucose (FBG) of \>126 mg/dL, or of CF-related diabetes as determined according to the Cystic Fibrosis Foundation (CFF) Consensus Conference of January 1999 (Section IX Part II), that is: a) FBG \>126 mg/dL (7.0 millimoles per liter \[mmol/L\]) on two or more occasions b)FBG \>126 mg/dL (7.0 mmol/L) plus casual (without regard to time of day or last meal consumed) glucose level \>200 mg/dL (11.1 mmol/L) c)Casual (previously called random) glucose levels \>200 mg/dL (11.1 mmol/L) on two or more occasions with symptoms
• Participants using an enzyme preparation in excess of 10,000-lipase units/kg/day
• Participants using an immunosuppressive drug
• Participants who are expecting an inability to tolerate the washout period and/or the placebo treatment
• Participants participating in an investigational study of a drug, biologic, or device not currently approved for marketing, within 30 days of screening visit
• Female participants who are pregnant or breastfeeding, or unwilling to use effective birth control during study
• Participants with any condition that would, in the investigator's opinion, limit the participant's ability to complete the study

Sponsors & Collaborators

• Forest Laboratories: lead

Study Sites (1)

University of Texas Health Center at Tyler

Tyler, Texas, 75708, United States

Location

Related Publications (1)

• Wooldridge JL, Heubi JE, Amaro-Galvez R, Boas SR, Blake KV, Nasr SZ, Chatfield B, McColley SA, Woo MS, Hardy KA, Kravitz RM, Straforini C, Anelli M, Lee C. EUR-1008 pancreatic enzyme replacement is safe and effective in patients with cystic fibrosis and pancreatic insufficiency. J Cyst Fibros. 2009 Dec;8(6):405-17. doi: 10.1016/j.jcf.2009.07.006. Epub 2009 Aug 15.

  PMID: 19683970 DERIVED

MeSH Terms

Conditions

Cystic Fibrosis; Exocrine Pancreatic Insufficiency

Condition Hierarchy (Ancestors)

Pancreatic Diseases; Digestive System Diseases; Lung Diseases; Respiratory Tract Diseases; Genetic Diseases, Inborn; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infant, Newborn, Diseases

Results Point of Contact

• Title: Robert Winkler, MD, VP, Clinical Development and Operations
• Organization: Aptalis Pharma US, Inc.

1- 800- 472- 2634

Study Officials

• Aptalis Medical Information

  Forest Laboratories

  STUDY DIRECTOR

Publication Agreements

• PI is Sponsor Employee: No
• Restriction Type: OTHER
• Restrictive Agreement: Yes

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 27, 2006
• First Posted: February 28, 2006
• Study Start: May 1, 2006
• Primary Completion: November 1, 2006
• Study Completion: November 1, 2006
• Last Updated: March 16, 2017
• Results First Posted: April 4, 2014

Record last verified: 2017-02

Locations

US (1)