Phase III Study of ISU302 in Patients With Type 1 Gaucher Disease

NCT02770625 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2017-07-12

Study results available
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Summary

The purpose of this study is to evaluate the safety and efficacy of ISU302 in patients with Type 1 Gaucher disease.

Conditions

  • Gaucher Disease, Type 1

Interventions

DRUG

ISU302

60 U/kg given intravenously

Sponsors & Collaborators

  • ISU Abxis Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Amel El Beshlawy, Prof. · Abou El Reesh Children's Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
2 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-09-30
Primary Completion
2013-03-31
Completion
2014-08-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02770625 on ClinicalTrials.gov