A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in Subjects With Diabetes Mellitus Type 2

PHASE4WithdrawnINTERVENTIONAL
0
Timeline

Start Date

November 30, 2013

Primary Completion Date

August 31, 2014

Study Completion Date

August 31, 2014

Conditions
Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2
Interventions
DRUG

Creon

Creon 25000 (2 capsules per meal 3 times per day and 1 capsule/snack 2 times per day) during 12 weeks

DRUG

Creon 25000 matching Placebo

Creon 25000 placebo matching capsules (2 capsules per meal 3 times per day and 1 capsule/snack 2 times per day) during 12 weeks

Trial Locations (10)

15706

Site reference no. 112495, Santiago de Compostela

28034

Site reference no. 112519, Madrid

29071

Site reference no. 112520, Málaga

35415

Site reference no. 113476, Pohlheim

40002

Site reference no. 112518, Segovia

41014

Site reference no. 112496, Seville

44789

Site reference no. 113456, Bochum

60594

Site reference no. 113477, Frankfurt

89073

Site reference no. 113475, Ulm

05004

Site reference no. 112517, Ávila

Sponsors

Lead Sponsor

Collaborators (3)

All Listed Sponsors
collaborator

Nuvisan

UNKNOWN

collaborator

Datamap

INDUSTRY

collaborator

ClinIntel

INDUSTRY

collaborator

Catalent

INDUSTRY

lead

Abbott

INDUSTRY

NCT02009410 - A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in Subjects With Diabetes Mellitus Type 2 | Biotech Hunter | Biotech Hunter