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

S

Solvay

Status and phase

Completed
Phase 3

Conditions

Cystic Fibrosis
Pancreatic Exocrine Insufficiency

Treatments

Drug: Pancrelipase Delayed Release

Study type

Interventional

Funder types

Industry

Identifiers

NCT00775528
S245.3.128

Details and patient eligibility

About

This study will assess the safety and tolerability of pancrelipase delayed release capsules in subjects up to 6 years of age with Pancreatic Exocrine Insufficiency (PEI) due to Cystic Fibrosis.

Enrollment

19 patients

Sex

All

Ages

1 month to 6 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Confirmed Cystic Fibrosis (CF) diagnosis by two positive chloride sweat tests or gene analysis
  • Current or historical human fecal elastase < 50µg/gstool
  • Weight greater than 3.75 kg
  • Age 1 month to 6 years
  • 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

Exclusion criteria

  • Ileus or acute abdomen
  • History of fibrosing colonopathy, Celiac disease, gastrectomy, Crohn´s disease and small bowel surgery other than minor resection due to meconium ileus without resulting in malabsorption syndrome
  • 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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

19 participants in 1 patient group

A
Experimental group
Treatment:
Drug: Pancrelipase Delayed Release

Trial contacts and locations

12

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Data sourced from clinicaltrials.gov

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