Trial intelligence / Profile preview

Creon 40,000 MMS in Pancreatic Exocrine Insufficiency

NCT00705978Phase 3Completed

Sponsor
Abbott Laboratories
Start
Jun 2008
Primary completion
May 2010
Modality
Replacement Enzymes
Countries
1
01

Overview

Phase 3, randomised, double-blind trial in pancreatic exocrine insufficiency (EPI) comparing Creon 40,000 MMS with Placebo (2 arms). Primary endpoint: Coefficient of Fat Absorption at 7 days. Started Jun 2008; status: completed.

02

Drugs

LipaCreon
03

Conditions

pancreatic exocrine insufficiency (EPI)

Beyond the preview

Go deeper on NCT00705978.

Study design, results and competitive context are available in the Gosset platform where reported.

Study design & results

Available in the Gosset platform where reported.

Competitive context

Available in the Gosset platform where reported.

Bring the full picture into focus.

See how Gosset can support your research on NCT00705978.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call