B001 injection
DrugB001 injection 50mg/5mL Intravenous solution
NCT Number: NCT05145361
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Early Phase 1
Beijing Tiantan Hospital Capital Medical University, Beijing, Beijing Municipality, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
B001 injection 50mg/5mL Intravenous solution
Placebo 5mL Intravenous solution
Time frame: Up to 18 days.
Measurement of DLT in all subjects.
Time frame: Up to 1 year
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
To characterize the PK (Pharmacokinetics) of B001.
Time frame: Through study completion, up to 2 years
Time frame: Through study completion, up to 2 years
Time frame: Through study completion, up to 2 years
The EDSS provides a total score on a scale that ranges from 0 to 10 in 0.5 increments that represent higher levels of disability. Increasing disability is reflected in an increasing EDSS score.
Time frame: Through study completion, up to 2 years
Contact information is provided by the study sponsor or research team.
Shanghai Pharmaceuticals Holding Co., Ltd
Industry
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)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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