A Study to Identify and Characterize LAL-D Patients in High-risk Populations

NCT02345421 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 640

Last updated 2016-05-24

No results posted yet for this study

Summary

The objective of this study is to determine the frequency of Lysosomal Acid Lipase Deficiency (LAL D) by lysosomal acid lipase (LAL) enzyme activity assay in patients who are considered to be at risk.

Conditions

  • Lysosomal Acid Lipase Deficiency

Sponsors & Collaborators

  • Alexion Pharmaceuticals, Inc.

    lead INDUSTRY

Eligibility

Min Age
2 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2015-09-30
Completion
2015-10-31

Countries

  • United States

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 NCT02345421 on ClinicalTrials.gov