Comparison of PK and Tolerability of MSB11022 Administered by AI or PFS

PHASE1CompletedINTERVENTIONAL
Enrollment

216

Participants

Timeline

Start Date

July 15, 2019

Primary Completion Date

March 17, 2020

Study Completion Date

March 17, 2020

Conditions
Rheumatoid ArthritisPolyarticular Juvenile Idiopathic ArthritisPsoriatic ArthritisAnkylosing SpondylitisCrohn DiseaseUlcerative ColitisPlaque PsoriasisPediatric Plaque PsoriasisPediatric Crohns DiseaseHidradenitis SuppurativaNon-infectious Uveitis
Interventions
DRUG

40 mg MSB11022

Single dose, as a solution, administered subcutaneously, using an auto-injector.

DRUG

40 mg MSB11022

Single dose, as a solution, administered subcutaneously, using a pre-filled syringe.

Trial Locations (2)

66219

PRA Health Sciences (PRA) - Early Development Services (EDS), Lenexa

84124

PRA-EDS, Salt Lake City

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

PRA Health Sciences

INDUSTRY

lead

Fresenius Kabi SwissBioSim GmbH

INDUSTRY