NCT05199571CompletedPhase 4
Study of Efficacy and Safety of Ofatumumab in Relapsing Multiple Sclerosis (RMS) Patients in China
A 12-month, Open-label, Prospective, Multicenter, Interventional, Single-arm Study Assessing the Efficacy and Safety of Ofatumumab 20 mg Subcutaneous (s.c.) Injection in Relapsing Multiple Sclerosis (RMS) Patients in China
Source: ClinicalTrials.gov · Last updated 13 Jan 2026
Brief summary (registry, in English)
The purpose of this study was to evaluate the efficacy and safety of ofatumumab s.c. in adult participants with relapsing multiple sclerosis (RMS) in China.
- Status (registry)
- Completed
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 99 (actual)
- First submitted
- 6 Jan 2022
- Start date
- Jul 2022
- Primary completion date
- Feb 2025
- Lead sponsor
- Novartis Pharmaceuticals
- Diseases
- Multiple sclerosis
- NCT number
- NCT05199571
What you commit to
- Study type: Interventional · Phase 4
- Participants enrolled: 99
- From Jul 2022 to the primary completion date, Feb 2025
- 14 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Women of child-bearing potential unless using effective methods of contraception while taking study treatment and for at least 6 months after stopping medication
- Have received any live or live-attenuated vaccines within four weeks prior to first study drug administration
- Have been treated with medications as specified or within timeframes specified in the protocol
Other illness
- Participants with primary progressive MS (PPMS) or secondary progressive MS (SPMS) without disease activity
- Participants meeting criteria for neuromyelitis optica spectrum disorder (NMOSD)
- Participants with an active chronic disease of the immune system other than MS
- Participants with active hepatitis B disease
- Participants with active systemic infections (including but not limited to active COVID-19 infection) or known to have AIDS or to test positive for HIV antibody at Screening
- Participants at high risk of developing or having reactivation of syphilis or tuberculosis
- Any other disease or condition that could interfere with participation in the study according to the study protocol, or with the ability of the participants to cooperate and comply with the study procedures.
Other
- Pregnant or nursing (lactating) women
- Participants with neurological findings consistent with PML or confirmed PML
Who the study is looking for
- Male or female Chinese aged 18-55 years (inclusive) at their enrollment of the study (signing the study consent form).
- Clinical definite diagnosis of RMS according to the 2017 Revised McDonald criteria (Thompson et al 2018, and the documentation prior to their enrollment to the study (signing the study consent form) of:
- Two documented relapses during the past 2 years, or
- One documented relapse during the last year, or
- A positive Gd-enhancing MRI scan during the year prior to Screening. Note: Screening MRI scan may be used if no positive Gd-enhancing scan exists from prior year.
- Disability status with an EDSS score of 0 - 5.5 (inclusive) at Screening.
- Neurologically stable within 1 month prior to both Screening and Baseline (including no MS relapse in this period).
Age in the registry: 18 years to 55 years · Sex: All · Does not accept healthy volunteers
Sites (14)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.