An Observational Study of Patients With Lysosomal Acid Lipase Deficiency/Cholesteryl Ester Storage Disease Phenotype

NCT01528917 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 49

Last updated 2016-07-20

No results posted yet for this study

Summary

This is a Natural History study to characterize key aspects of the clinical course of late onset Lysosomal Acid Lipase (LAL) Deficiency/ Cholesteryl Ester Storage Disease (CESD).

Conditions

  • Cholesterol Ester Storage Disease(CESD)
  • Lysosomal Acid Lipase Deficiency

Sponsors & Collaborators

  • Alexion Pharmaceuticals, Inc.

    lead INDUSTRY

Eligibility

Min Age
5 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2013-01-31
Completion
2013-05-31

Countries

  • United States
  • Canada
  • Czechia
  • France
  • Italy
  • Poland
  • Switzerland
  • United Kingdom

Study Locations

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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 NCT01528917 on ClinicalTrials.gov