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NCT03198897: BioHoFH

Biomarker for Homozygous Familial Hypercholesterolemia (BioHoFH)

Withdrawn Last updated 13 February 2023
What this trial tests

trial in Lipoprotein Lipase Deficiency. Withdrawn.

Timeline
20 August 2018
Primary endpoint
28 February 2021
28 February 2021

Quick facts

Lead sponsorCENTOGENE GmbH Rostock
StatusWithdrawn
Study typeOBSERVATIONAL
Start date20 August 2018
Primary completion28 February 2021
Estimated completion28 February 2021
Sites4 locations across Sri Lanka, Germany, India

Conditions studied

Sponsor

CENTOGENE GmbH Rostock

Who can join

2 Months and older, any sex, with Lipoprotein Lipase Deficiency or Inborn Error of Lipid Metabolism. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Development of a new MS-based biomarker for the early and sensitive diagnosis of Homozygous familial Hypercholesterolemia from blood

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Genetic Testing for Familial Hypercholesterolemia: Health Technology Assessment.
    Ontario Health (Quality) . · · 2022 · cited 6× · PMID 36158868

Verify or expand the search:

Other recruiting trials for Lipoprotein Lipase Deficiency

Currently open trials in the same condition.

Other CENTOGENE GmbH Rostock trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03198897.

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