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NCT05799118: INHERENT

Study of the Role of Genetic Modifiers in Hemoglobinopathies

Recruiting now Last updated 20 March 2024
What this trial tests

trial testing GWAS in Sickle Cell Disease in 30,000 participants. Currently enrolling.

Timeline
1 October 2022
Primary endpoint
30 September 2027
30 September 2027

Quick facts

Lead sponsorCyprus Institute of Neurology and Genetics
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment30,000
Start date1 October 2022
Primary completion30 September 2027
Estimated completion30 September 2027
Sites26 locations across Denmark, Angola, Italy, Pakistan, Greece, Cyprus, Malaysia, Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Cyprus Institute of Neurology and Genetics

Who can join

2 and older, any sex, with Sickle Cell Disease or Thalassemia, Beta. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will investigate the role of genetic modifiers in hemoglobinopathies through a large-scale, multi-ethnic genome-wide association study (GWAS).

Publications & conference data

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

  1. Ethical and regulatory requirements for conducting researcher-driven large-scale multinational genetic haematological studies: the INHERENT experience.
    Didio A, Giannuzzi V, Archer N, Gani E, et al · · 2025 · cited 2× · PMID 40765057 · DOI 10.1186/s12961-025-01375-z

Verify or expand the search:

Other trials of GWAS

Trials testing the same drug.

Other recruiting trials for Sickle Cell Disease

Currently open trials in the same condition.

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/NCT05799118.

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