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Terminated No phase listed Observational

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

ClinicalTrials.gov ID: NCT02345421

Public ClinicalTrials.gov record NCT02345421. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 10:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study to Identify the Frequency of Lysosomal Acid Lipase Deficiency in At-Risk Patient Populations

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02345421
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Alexion Pharmaceuticals, Inc.
Industry
Enrollment
640 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
2 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2014 (Type not available)
Primary completion
Sep 2015 (Actual)
Completion
Oct 2015 (Actual)
Last update posted
May 24, 2016

2014 – 2015

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Phoenix Arizona — —
Not listed Los Angeles California — —
Not listed San Francisco California — —
Not listed Gainesville Florida — —
Not listed Jacksonville Florida — —
Not listed Miami Florida — —
Not listed New Orleans Louisiana — —
Not listed Minneapolis Minnesota — —
Not listed The Bronx New York — —
Not listed Durham North Carolina — —
Not listed Oklahoma City Oklahoma — —
Not listed Portland Oregon — —
Not listed Houston Texas — —
Not listed San Antonio Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02345421, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 24, 2016 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02345421 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →