Clinical Trials Browser

Recruiting × Genetic Diseases, Inborn × Clear all

NCT06330441 2026-04-21

ScrePan

Phase NA Recruiting

Genetic Diseases, Inborn, Pancreatitis, Chronic

NCT05361811 2026-02-19

Acceptance and Commitment Therapy for Caregivers of Children With a RASopathy: An Internal Pilot Feasibility Study and Follow-up Randomized Controlled Trial

Phase NA Recruiting

CNSDermatologic

Cardiofaciocutaneous syndrome, Legius syndrome, Neurofibromatosis 1, Noonan Syndrome, Genetic Diseases, Inborn, Costello Syndrome

NCT03568630 2026-02-02

Blood Markers of Early Pancreas Cancer

Gastrointestinal

Diabetes Mellitus, Type 2, Pancreatic Cyst, Prediabetic State, Genetic Predisposition to Disease, Genetic Diseases, Inborn, Pancreatitis, Chronic

NCT06549725 2025-08-01

Clinical Performance of Medical Device Software "Lipidica 1.0" for Processing Data Generated by Lipidomic Analysis in Pancreatic Cancer Screening

Phase NA Recruiting

Gastrointestinal

Pancreatic Neoplasms, Genetic Diseases, Inborn, Pancreatitis, Chronic

NCT05587439 2025-07-10

INHERIT

Lung Neoplasms, Genetic Predisposition to Disease, Genetic Diseases, Inborn

NCT04880356 2024-11-19

Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.

2-Hydroxyglutaricaciduria, Fahr's disease, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, Methylmalonic acidemia with homocystinuria, Undiagnosed Diseases, Adrenoleukodystrophy, Cysts, Hepatolenticular Degeneration, Leukodystrophy, Globoid Cell, Leukodystrophy, Metachromatic, Metabolic Diseases, Nervous System Diseases, Sphingolipidoses, Xanthomatosis, Cerebrotendinous, Pelizaeus-Merzbacher Disease, Genetic Diseases, Inborn, Rare Diseases, Alexander Disease, Leukoencephalopathies

NCT05898009 2024-08-22

CanSeR-OGen

Phase NA Recruiting

Breast Neoplasms, Genetic Diseases, Inborn

NCT04531696 2024-06-28

UPTIDER

Phase NA Recruiting

Breast Neoplasms, Genetic Diseases, Inborn

NCT04682470 2022-03-02

COMPRAYA

Infertility, Neoplasms, Neoplasms, Second Primary, Genetic Diseases, Inborn