A Clinical Trial of BAT4406F Injection in Patients with Neuromyelitis Optica Spectrum Disorders
- Conditions
- Optic Neuromyelitis Spectrum Disease
- Interventions
- Drug: BAT4406F InjectionDrug: BAT4406F Placebos
- Registration Number
- NCT06044350
- Lead Sponsor
- Bio-Thera Solutions
- Brief Summary
This is a phase II/III multicenter, randomized, double-blind, placebo-controlled study, to investigate the efficacy and safety of BAT4406F injection in patients with neuromyelitis optica lineage disease (NMOSD) who are positive for aquaporin 4 antibody (AQP4-IgG) .
- Detailed Description
This study was a phase II/III multicenter, randomized, double-blind, placebo-controlled study, which was divided into screening period (4 weeks) , randomized control period (RCP) , and open-label period (Olp)A total of 162 subjects were enrolled during the screening period and randomly assigned 2:1 to either the BAT4406F group or the placebo group after randomization on Day 1 of the RCP, subjects would receive BAT4406F (at a dose of 500mg) or placebo, intravenously, at D 1 and D 182, respectively.
If any of the following conditions occur, subjects can enter OLP from RCP: 1. Subjects who complete the 52-week RCP study without recurrence of NMOSD can enter Olp within 14 days after the end of the RCP study. 2. In the stage of RCP, NMOSD recurred. After rescue therapy, the patients with stable condition could enter OLP within 28 days after diagnosis. Subjects continued to participate in the RCP study if they were not identified by CEC as having a relapse upon examination. 3. When a protocol-defined first relapse event of 35 cases is observed, or when all 162 subjects have completed randomization and 12 months have elapsed since the first dose in the last of these subjects, or when recommended by the Independent Data Monitoring Committee (IDMC) , the RCP study should be stopped for enrolled subjects, and all enrolled subjects at the RCP stage should stop the RCP study within 14 days of entry into OLP, after which subjects will receive BAT4406F injection at the same dose as RCP, at d 1 of OLP. After termination of the RCP study with BAT4406F every 6 months, subjects were given the option of enrolling in the OLP study.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 162
- Age greater than or equal to the age of 18 and less than or equal to 65 patients, gender not limited;
- Met the 2015 international NMO diagnostic panel (IPND) criteria for NMOSD, And AQP4-IGG positive patients
- Screening before 2 times at least 2 years experience with clinical records of relapse，or experienced at least 1 clinically documented recurrence within 1 year prior to screening
- For subjects who had a relapse before screening, symptoms needed to be stable for at least 4 weeks before randomization
- Into the group of former dosage of corticosteroids under 30 mg and prednisone equivalent，and the trial drug must be used within a month after the withdrawal of hormones
- The score of EDSS 7 or less
- Has the fertility of men and women must agree during treatment and 6 months after the last dose of using effective birth control method;
- Agreed to participate in trials, and books to sign the informed consent
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CD19 + b-cell count below the lower limit of normal, b-cell-scavenger drugs used 6 months before baseline or within 5 half-lives of the drug, whichever is older (including but not limited to Rituximab, enalizumab, etc.) ;
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6 months prior to the baseline used other monoclonal antibody therapy;Baseline used within five half-life before other biological preparation;
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Used it for 3 months prior to the baseline McCaw phenol ester, azathioprine and methotrexate;6 months prior to the baseline using cyclophosphamide;Baseline before five half-life
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Within a month before the filter used intravenous immunoglobulin (IVIG), plasma exchange (PE);
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Within 4 weeks before screening received vaccine or live attenuated;Within 2 weeks before the baseline received inactivated vaccine;Baseline received within 4 weeks before the new coronavirus vaccine
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In another clinical study and the baseline from the test drug treatment under three months or 5 half-life of the drug (the long time limit shall prevail);
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This test for monoclonal antibody has a history of allergies, known in drug allergy patients;Serious drug allergy or for two or over two kinds of food or drugs；
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6 months prior to screening, except NMOSD need continuous oral or intravenous glucocorticoid dose > 20 mg/day of any more than 21 days
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Abnormal liver, kidney and bone marrow reserve
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HIV positive at HIV history or enrollment screening; History of hepatitis B Andor hepatitis C or Hepatitis B surface antigen (HBSAG) positivity at screening [ or Hepatitis B core antibody positive, hepatitis B surface antibody negative, Hepatitis B virus deoxynucleotides (HBV DNA) quantification exceeding normal range ] ; Or Hepatitis C virus (HCV) antibody positive [ with HCV-rna quantitation exceeding the normal range ] , Treponema pallidum antibody positive at the time of enrollment;
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Comply with any of the following subjects a latent or active TB infection related standards:
- Current or past people with active TB;
- In history and/or physical examination during filter tip physical signs or symptoms of active TB;
- Recent close contact with people with active TB;
- At the time of screening, the positive result of TB infected T cells was found. A test could be repeated if the subject's first tb-infected t-cell test result was inconclusive, and the patient was excluded from this study if the test result was inconclusive (or positive) again.
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Covid-19 infection was diagnosed with clinical symptoms or signs consistent with 2019 coronavirus (COVID-19) infection (eg, fever, dry cough, dyspnea, sore throat, and fatigue) within 4 weeks before screening or during screening, or upon appropriate laboratory testing (at the discretion of the investigator or in accordance with local regulations) . If COVID-19 infection is confirmed before screening, appropriate laboratory testing is required to confirm that the infection has been cured;
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Suffering from metabolic, hematological, renal, hepatic, pulmonary, neuroendocrine, cardiac, infectious, gastrointestinal or other autoimmune diseases, the researchers believe there is an unacceptable risk to patients, or it may affect NMOSD assessment;
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According to the researchers, there was a history of drug and alcohol abuse (drinking 14 units of alcohol per week: 1 unit = 285 mL of beer, or 25 mL of spirits, or 125 mL of wine) in the 12 months before screening；
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Subjects who are unable to undergo an MRI scan (for example, are allergic to Gd-containing MRI contrast media, have a pacemaker, defibrillator, or other metallic object with internal or external limitations to performing an MRI scan) ;
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Pregnant or lactating women, and screening or baseline pregnancy test positive female subjects;
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Researchers think that the other does not fit to participate in this study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental group：BAT4406F BAT4406F Injection RCP：Intravenous infusion; Dosage:500mg/time; Time of administration:The drug was given at D 1 and D 182 respectively OLP：Intravenous infusion; Dosage:500mg/time; Time of administration: After D1 dosing, Every 6 months to 1 times Control group：BAT4406F Placebos BAT4406F Placebos RCP：Intravenous infusion; Dosage:500mg/time; Time of administration:The drug was given at D 1 and D 182 respectively OLP：Intravenous infusion; Dosage:500mg/time; Time of administration: After D1 dosing, Every 6 months to 1 times
- Primary Outcome Measures
Name Time Method Pharmacokinetics（PK） Through study completion,up to 49 months. And OLP maximum period for 3 years. Vd
Immunogenicity evaluation RCP:in Day84、Day181、Day252、Day364. OLP: in Day84、Day181、Day252、Day364 of every years.And OLP maximum period for 3 years The titers of Ada positive samples
Pharmacodynamics RCP:in Day84、Day182、Day280、Day364. OLP: in Day1、Day84、Day182、Day280、Day364 of every years.And OLP maximum period for 3 years AQP4-IgG levels were measured.
- Secondary Outcome Measures
Name Time Method Adverse events（AE） Through study completion,up to 49 months. And OLP maximum period for 3 years. Adverse events (AE) is happening, is happening because of adverse events leading to withdrawal Adverse events associated with drugs The occurrence of Serious adverse events (SAE)
physical examination Through study completion,up to 49 months. And OLP maximum period for 3 years. Number of participants with abnormal physical examination findings
Vital signs Through study completion,up to 49 months. And OLP maximum period for 3 years. Number of participants with abnormal vital signs
electrocardiogram（ ECG ） Through study completion,up to 49 months. And OLP maximum period for 3 years. Number of participants with abnormal ECG readings
Laboratory tests Through study completion,up to 49 months. And OLP maximum period for 3 years. Number of participants with abnormal laboratory test results
Injection site reactions Through study completion,up to 49 months. And OLP maximum period for 3 years. Number of participants with injection site reactions
Trial Locations
- Locations (45)
Shandong University Qilu Hospital
🇨🇳Jinan, China
Xiehe hospital affiliated to tongji medical college huazhong university of science and technology
🇨🇳Wuhan, China
Qingdao municipal hospital
🇨🇳Qingdao, China
Beijing Hospital
🇨🇳Beijing, China
The First Affiliated Hospital of the Baotou Medical College of Inner Mongolia University of Science and Technology
🇨🇳Baotou, China
The first hospital of Peking University
🇨🇳Beijing, China
China-japan friendship Hospital
🇨🇳Beijing, China
The Central South University Xiang Ya Hospital
🇨🇳Changsha, China
Xiangya 2nd hospital of central south university
🇨🇳Changsha, China
First affiliated hospital of fujian medical university
🇨🇳Fuzhou, China
The first affiliated hospital of Dalian Medical University
🇨🇳Dalian, China
First affiliated hospital of chongqing medical university
🇨🇳Chongqing, China
The first hospital affiliated to sun yat-sen university
🇨🇳Guangzhou, China
The first People's Hospital of Guangzhou
🇨🇳Guangzhou, China
The third hospital affiliated to sun yat-sen university
🇨🇳Guangzhou, China
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
🇨🇳Guangzhou, China
Anhui Provincial Hospital
🇨🇳Hefei, China
Second Affiliated Hospital of Anhui Medical University
🇨🇳Hefei, China
People's Hospital of Zhejiang province
🇨🇳Hangzhou, China
Jingzhou Central Hospital
🇨🇳Jingzhou, China
First Affiliated Hospital of the Kunming Medical University
🇨🇳Kunming, China
Second Affiliated Hospital of Nanchang University
🇨🇳Nanchang, China
Affiliated Hospital of North Sichuan Medical College
🇨🇳Nanchong, China
The first People's Hospital of Nantong
🇨🇳Nantong, China
Southeast university affiliated zhongda hospital
🇨🇳Nanjing, China
The Chinese people's liberation army general hospital in eastern theater
🇨🇳Nanjing, China
Mount Hua Hospital affiliated to Fudan University
🇨🇳Shanghai, China
Shuguang hospital affiliated to Shanghai University of Traditional Chinese medicine
🇨🇳Shanghai, China
Zhongshan hospital affiliated to Fudan University
🇨🇳Shanghai, China
Shenzhen city people's hospital
🇨🇳Shenzhen, China
Second Hebei Medical University Hospital
🇨🇳Shijia Zhuang, China
Tianjin Medical University General Hospital
🇨🇳Tianjin, China
First Affiliated Hospital of Suzhou University
🇨🇳Suzhou, China
The first hospital of shanxi medical university
🇨🇳Taiyuan, China
The first hospital affiliated to wenzhou medical college
🇨🇳Wenzhou, China
The Third Hospital of Hebei Medical University
🇨🇳Shijiazhuang, China
The Second Affiliated Hospital of Suzhou University
🇨🇳Suzhou, China
Tongji hospital affiliated to tongji medical college huazhong university of science and technology
🇨🇳Wuhan, China
Wuxi city people's hospital
🇨🇳Wuxi, China
Henan province people's hospital
🇨🇳Zhengzhou, China
Second Affiliated Hospital of the People's Liberation Army Air Force Military Medical University
🇨🇳Xi'an, China
Yan 'an University Xianyang Hospital Co. , Ltd.
🇨🇳Xianyang, China
Xi'an high-tech Hospital Co. , Ltd.
🇨🇳Xi'an, China
Zhengzhou university first affiliated hospital
🇨🇳Zhenzhou, China
Drum Tower Hospital affiliated to Medical College of Nanjing University
🇨🇳Nanjing, China