JR-141
DrugIV infusion, 2.0 mg/kg/week
NCT Number: NCT03568175
A Phase II/ III multicenter, open-label, single-group, designed to evaluate the efficacy and safety of study drug for the treatment of the MPS II.
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Interventional
Phase 2 / Phase 3
Fukui Clinical site, Fukui, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
IV infusion, 2.0 mg/kg/week
Time frame: Baseline to 52 weeks
Time frame: Baseline, 24-26 weeks, 50-52 weeks
Time frame: Baseline, 24-26 weeks, 50-52 weeks
Time frame: Baseline, 25 weeks, 52 weeks
Time frame: Baseline, 25 weeks, 52 weeks
Time frame: Baseline, 25 weeks, 52 weeks
Time frame: Baseline, 25 weeks, 52 weeks
Time frame: Baseline, 25 weeks, 52 weeks
Time frame: Baseline, 25 weeks, 52 weeks
Item 9 will be administrated only in patients judged by the investigator or subinvestigator to be possible to perform the 6-minutes walk test
Time frame: Baseline, 25 weeks, 52 weeks
Time frame: Baseline to 25 weeks
Time frame: Baseline, 25 weeks, 52 weeks
Time frame: 25, 52 weeks
Time frame: 25, 52 weeks
Time frame: 25, 52*weeks
*Drug concentration in Cerebrospinal Fluid at 52 Weeks is applicable only for subjects to be enrolled in extension study .
JCR Pharmaceuticals Co., Ltd.
Industry
A Phase II/III Study of JR-141 in Patients With Mucopolysaccharidosis II
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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