Optic Neuritis Clinical Trials

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Efficacy and Safety of Ofatumumab in AQP4-IgG Seropositive NMOSD: an Open-label, Single-arm, Multicentre Prospective Pilot Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This is an open-label, single-arm, multicentre prospective pilot study to assess the efficacy and safety of ofatumumab in patients with AQP4-IgG seropositive neuromyelitis optica spectrum disorder (NMOSD) in China.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of NMOSD according to the 2015 International Panel Diagnostic Criteria for NMOSD with AQP4-IgG.

• Clinical evidence of at least 2 relapses (including first attack) in past 24 months with at least 1 relapse occurring in the preceding 12 months.

• Adults aged ≥18 years old.

• Expanded disability status scale (EDSS) score between 0 and 7.5 (inclusive).

• Provision of written informed consent to participate in this study.

• Only oral corticosteroids were permitted at screening (≤10mg equivalent per day), which should be terminated within one month.

• Effective contraception was used for female patients with fertility during the treatment or at least 3 months after stopping medication.

Locations
Other Locations
China
Tangdu Hospital
RECRUITING
Xi'an
Contact Information
Primary
Jun Guo, M.D.
guojun_81@163.com
86-29-8477 8844
Backup
Yan Jia, M.S.
neurologist_jiayan@163.com
86-29-8471 7483
Time Frame
Start Date: 2022-06-28
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 5
Treatments
Experimental: Ofatumumab
The enrolled patients will receive ofatumumab (20 mg/0.4 ml) subcutaneously administered at baseline, Day 7, Day 14 and monthly thereafter. Patients will receive ofatumumab therapy for a total of 48 weeks.
Sponsors
Collaborators: Henan Provincial People's Hospital
Leads: Tang-Du Hospital

This content was sourced from clinicaltrials.gov