Study to Evaluate Safety and Efficacy of Oral MP1032 in Psoriasis Patients

PHASE2CompletedINTERVENTIONAL
Enrollment

46

Participants

Timeline

Start Date

May 31, 2016

Primary Completion Date

December 31, 2016

Study Completion Date

February 28, 2017

Conditions
PsoriasisPlaque Psoriasis
Interventions
DRUG

MP1032

hard gelatine capsules containing 50 mg MP1032 as active ingredient

DRUG

Placebo

hard gelatine capsules without active ingredient

Trial Locations (4)

10783

Rothaar Studien GmbH, Berlin

14050

PAREXEL International GmbH, Klinikum Westend, Berlin

79100

Gemeinschaftspraxis Prof. Dr. Vanscheidt und Dr. Ukat, Freiburg im Breisgau

01069

Klinische Forschung Dresden GmbH, Dresden

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

MetrioPharm AG

INDUSTRY