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Completed Phase 3 Interventional Results available

A Study to Investigate the Effect of Delayed Release Pancrelipase on Maldigestion in Patients With Exocrine Pancreatic Insufficiency Due to Chronic Pancreatitis and Pancreatectomy

ClinicalTrials.gov ID: NCT00414908

Public ClinicalTrials.gov record NCT00414908. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 5:33 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study assessed the effect of pancrelipase delayed release capsules on fat and nitrogen absorption in subjects with PEI due to Chronic Pancreatitis and Pancreatectomy. There was a run-in with a 5-day of single-blind placebo treatment, followed by a 7-day Double-blind period and a 6-month Open-Label Follow-up.

Study identification

NCT ID
NCT00414908
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
52 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2007 (Type not available)
Primary completion
Aug 2008 (Actual)
Completion
Dec 2009 (Actual)
Last update posted
Aug 10, 2011

2007 – 2009

United States locations

U.S. sites
23
U.S. states
19
U.S. cities
23
Facility City State ZIP Site status
Site 9 Scottsdale Arizona — —
Site 22 Bristol Connecticut — —
Site 7 Tampa Florida — —
Site 6 Atlanta Georgia — —
Site 17 Chicago Illinois — —
Site 30 Maywood Illinois — —
Site 14 Indianapolis Indiana — —
Site 15 Kansas City Kansas — —
Site 16 Lexington Kentucky — —
Site 12 New Orleans Louisiana — —
Site 3 Boston Massachusetts — —
Site 2 Ann Arbor Michigan — —
Site 29 Grand Rapids Michigan — —
Site 1 Tupelo Mississippi — —
Site 5 St Louis Missouri — —
Site 8 Cedar Knolls New Jersey — —
Site 20 Boone North Carolina — —
Site 4 Rutherford College North Carolina — —
Site 10 Cincinnati Ohio — —
Site 11 Cleveland Ohio — —
Site 21 Pittsburgh Pennsylvania — —
Site 13 Dallas Texas — —
Site 18 Richmond Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00414908, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 10, 2011 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00414908 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →