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NCT04925804

Unraveling Genetics of HypoPhosPhatasia (HPP Genetics)

Completed Last updated 29 December 2021
What this trial tests

trial in Hypophosphatasia in 16 participants. Completed in 2 December 2021.

Timeline
2 June 2021
Primary endpoint
2 December 2021
2 December 2021

Quick facts

Lead sponsorCENTOGENE GmbH Rostock
StatusCompleted
Study typeOBSERVATIONAL
Enrollment16
Start date2 June 2021
Primary completion2 December 2021
Estimated completion2 December 2021
Sites1 location across Germany

Conditions studied

Sponsor

CENTOGENE GmbH Rostock

Who can join

Eligibility, any sex, with Hypophosphatasia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Observational study to perform Whole Genome Sequencing in participants clinically suspected for HPP and negative for known pathogenic ALPL variants

Publications & conference data

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

  1. Whole genome sequencing in adults with clinical hallmarks of hypophosphatasia negative for ALPL variants.
    Seefried L, Petryk A, Del Angel G, Reder F, et al · · 2024 · cited 3× · PMID 39276275 · DOI 10.1007/s11033-024-09906-7

Verify or expand the search:

Other recruiting trials for Hypophosphatasia

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/NCT04925804.

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