A Switch-Over Study of the Safety and Efficacy of ISU302 in Patients With Type 1 Gaucher Disease

NCT02053896 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5

Last updated 2014-02-04

No results posted yet for this study

Summary

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

Conditions

  • Gaucher Disease

Sponsors & Collaborators

  • ISU Abxis Co., Ltd.

    lead INDUSTRY

Eligibility

Min Age
8 Years
Max Age
29 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2012-02-29
Completion
2012-02-29

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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 NCT02053896 on ClinicalTrials.gov