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NCT05145361RecruitingEarly phase 1

Clinical Study of B001 Injection in Subjects With Neuromyelitis Optic Spectrum Disorder (NMOSD)

A Phase Ib Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of B001 in Subjects With Aquaporin-4 Antibody (AQP4-IgG) Positive Neuromyelitis Optic Spectrum Disorder (NMOSD)

Source: ClinicalTrials.gov · Last updated 5 May 2026

Brief summary (registry, in English)

The objectives of this phase Ib study are to evaluate the efficacy, safety, pharmacokinetics, pharmacodynamics and immunogenic profiles of B001 in subjects with aquaporin-4 antibody (AQP4-IgG) positive NMOSD.

Status (registry)
Recruiting
Phase (registry)
Early phase 1
Study type
Interventional
Enrollment
45 (estimated)
First submitted
21 Nov 2021
Start date
Apr 2022
Primary completion date
Dec 2026
Lead sponsor
Shanghai Pharmaceuticals Holding Co., Ltd
NCT number
NCT05145361

What you commit to

  • Study type: Interventional · Early phase 1
  • Planned participants: 45
  • From Apr 2022 to the primary completion date, Dec 2026
  • 4 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

  • Any previous treatment with anti-CD20, eculizumab, anti-BLyS monoclonal antibody (e.g., belimumab), any other treatment for prevention of multiple sclerosis (MS) relapse (e.g., interferon, natalizumab, glatiramer acetate, fingolimod, teriflunomide or dimethyl fumarate) within 6 months prior to baseline.
  • Received immunosuppression such as azathioprine, mycophenolate mofetil, methotrexate, cyclophosphamide, tacrolimus, mitoxantrone, cyclosporine A, etc, and rug therapy, biological agents such as satralizumab, tocilizumab, eculizumab, etc, 3 months prior to the first administration.
  • Evidence of serious uncontrolled concomitant diseases that may preclude participant participation, as described; Other nervous system disease, cardiovascular disease, hematologic/hematopoiesis disease, respiratory disease, muscular disease, endocrine disease, renal/urologic disease, digestive system disease, congenital or acquired severe immunodeficiency.
  • Known active infection within 3 months prior to baseline
  • History of drug or alcohol abuse within 6 months prior to baseline
  • Receipt of any live or live attenuated vaccine within 4 weeks prior to baseline

Other illness

  • History of severe allergic reaction to a biologic agent
  • Evidence of chronic active hepatitis B or C
  • Evidence of active tuberculosis
  • Uncontrolled systemic diseases, including hypertension that cannot be effectively controlled after treatment (systolic blood pressure ≥150 mmHg and/or diastolic blood pressure ≥100 mmHg), diabetes, gastrointestinal diseases, etc.; or the investigator believes that there is anything inappropriate reasons for selection.

Lab values

  • Following laboratory abnormalities at screening\*:
    • White blood cells (WBC) \<4.0 x10\^3/microliter (μL)
    • Absolute neutrophil count (ANC)
    • Absolute lymphocyte count \<0.5 x10\^3/μL
    • Platelet count \<80 x 10\^9/ L
    • Aspartate aminotransferase (AST) or alanine aminotransferase

Other

  • Pregnancy or lactation.

Who the study is looking for

  • NMOSD as defined by either of the following 2015 criteria with anti-AQP4 antibody (Ab) seropositive status at screening
  • Clinical evidence of at least 1 documented relapse in last 12 months prior to screening
  • Expanded Disability Status Scale (EDSS) score from 0 to 7.5 inclusive at screening
  • Age 18 to 70 years, inclusive at the time of informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beijing Tiantan Hospital,Capital Medical University
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
First Hospital of Shanxi Medical University
Coordinator of this site? Confirm its status
TaiyuanChinaRecruiting
Tianjin Medical University General Hospital
Coordinator of this site? Confirm its status
TianjinChinaRecruiting
Tangdu Hospital, Fourth Military Medical University
Coordinator of this site? Confirm its status
Xi'anChinaRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.