Safety, Tolerability and Immunogenic Response of CV-MG01 in Patients With Myasthenia Gravis

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

March 31, 2016

Primary Completion Date

September 30, 2018

Study Completion Date

September 30, 2018

Conditions
Myasthenia Gravis
Interventions
BIOLOGICAL

CV-MG01

"3 consecutive subcutaneous injections of CV-MG01. The three injections are planned for each patient on Days 1, 29 (+/- 3 days) and 85 (+/- 7 days), respectively.~Two dose levels: low and high dose."

BIOLOGICAL

Placebo

3 consecutive subcutaneous injections of placebo. The three injections are planned for each patient on Days 1, 29 (+/- 3 days) and 85 (+/- 7 days), respectively.

Trial Locations (1)

2650

University Hospital, Antwerp, Edegem

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Aepodia

INDUSTRY

collaborator

University Hospital, Antwerp

OTHER

collaborator

Leiden University Medical Center

OTHER

lead

CuraVac

INDUSTRY

NCT02609022 - Safety, Tolerability and Immunogenic Response of CV-MG01 in Patients With Myasthenia Gravis | Biotech Hunter | Biotech Hunter