Atlas Trials

Genotype Expression and Phenotype of Endothelial Cells, Carrying an ACVRL1, ENG or SMAD4 Mutation, in Response to BMP9 for the Identification of New Therapeutic Targets in Hereditary Haemorrhagic Telangiectasia

Clinical trial NCT05632484 · COMPLETED

Trial details

NCT number
NCT05632484
Sponsor
Hospices Civils de Lyon
Status
COMPLETED
Phase
Not Applicable
Study type
INTERVENTIONAL
Hereditary Haemorrhagic Telangiectasia
Start date
2023-03-10
Primary completion
2023-05-20
Enrollment
16

View on ClinicalTrials.gov

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