Status:
COMPLETED
Phase III Clinical Trial of NPB-01 in Patients With Guillain-Barré Syndrome
Lead Sponsor:
Nihon Pharmaceutical Co., Ltd
Conditions:
Guillain-Barré Syndrome
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
Patients diagnosed with Guillain-Barré syndrome were confirmed based on the diagnostic criteria for Guillain-Barré syndrome. Patients who meet all inclusion criteria and do not conflict with the exclu...
Eligibility Criteria
Inclusion
- In principle, patients are able to receive study drug within 2weeks(with limits of 4weeks) from the start of symptoms.
- Patients with predominant motor neuropathy and Hughes's Functional Grade(FG) is grade4 or grade5(in this regard, if symptoms is progressive, patients with FG is grade3 involve in this study).
- Patients with plasmapheresis, steroids(in prednisolone equivalent, more than 100mg/day) and immune globulin therapy is no operation for this onset.
- Patients with greater than or equal to 18 years old at informed consent.
Exclusion
- Patients with history of shock for NPB-01.
- Patients with history of hypersensitivity for NPB-01.
- Patients with history of volatile organic solvent abuse, abnormal porphyrin metabolism, history of pharynx or cutaneous diphtheria, plumbism, tephromyelitis, botulism, hysterical paralysis, toxic neuropathy(nitrofurantoin, dapsone, organophosphorous compound), serious diabetic neuropathy,peripheral neuropathy due to HIV,impaired peripheral neuropathy except Guillain-Barré syndrome.
- Patients with malignancy at informed consent.
- Patients treated with immune globulin at 8 weeks before informed consent.
- Patients with IgA deficiency.
- Patients with impaired liver function.
- Patients with impaired renal function.
- Patients with cerebro- or cardiovascular disorders.
- Patients with high risk of thromboembolism.
- Patients with hemolytic/hemorrhagic anemia.
- Patients with decreased cardiac function.
- Patients with decreased platelet.
Key Trial Info
Start Date :
October 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2015
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT02221271
Start Date
October 1 2014
End Date
August 1 2015
Last Update
April 12 2017
Active Locations (1)
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1
Nihon Pharmaceutical Co., Ltd
Osaka, Japan