A Study of HBM9161 in NMOSD Patients

PHASE1CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

March 31, 2020

Primary Completion Date

December 3, 2021

Study Completion Date

December 24, 2021

Conditions
NMO Spectrum Disorder
Interventions
DRUG

HBM9161 Injection

Subcutaneous injection; Weekly administered for a period of 4 weeks. All subjects are treated with the testing drug, add on intravenous methylprednisolone (ivMP) with gradually reduce the dose then to oral prednisone. After the administration of the testing drug, if the subject's symptoms get worsen, a rescue therapy need to be adopted as based on Investigator's judgement, the testing drug injection should be discontinued.

Trial Locations (1)

Unknown

Nanfang Hospital, Guangzhou

All Listed Sponsors
lead

Harbour BioMed (Guangzhou) Co. Ltd.

INDUSTRY

NCT04227470 - A Study of HBM9161 in NMOSD Patients | Biotech Hunter | Biotech Hunter