Genetic Disease Clinical Trials

41 recruiting

Genetic Disease Trials at a Glance

48 actively recruiting trials for genetic disease are listed on ClinicalTrialsFinder across 6 cities in 24 countries. The largest study group is Not Applicable with 12 trials, with the heaviest enrollment activity in Boston, Paris, and Philadelphia. Lead sponsors running genetic disease studies include Boston Children's Hospital, Children's Hospital of Philadelphia, and Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University.

Browse genetic disease trials by phase

Treatments under study

About Genetic Disease Clinical Trials

Looking for clinical trials for Genetic Disease? There are currently 41 studies actively recruiting participants. Clinical trials offer access to new treatments before they are widely available, and every approved therapy in use today was first tested through a clinical trial.

Below you can browse trials, sign up for alerts when new Genetic Disease trials open, and view eligibility criteria for each study. Each listing includes the study phase, locations, and enrollment details.

Frequently Asked Questions

Common questions about Genetic Disease clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 120 of 48 trials

Recruiting

Adaptive Optics Retinal Imaging in Inherited and Acquired Retinal Disorders

Genetic DiseaseInherited Disease
The Hospital for Sick Children200 enrolled1 locationNCT05386134
Recruiting

The Natural History of Mitochondrial Diseases

Genetic DiseaseMitochondrial DiseasesNeurological Diseases or Conditions
Neuroscience Research Australia500 enrolled1 locationNCT06504433
Recruiting

Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network

Genetic Disease
National Human Genome Research Institute (NHGRI)20,000 enrolled33 locationsNCT02450851
Recruiting

Recruitment and Apheresis Collection of Peripheral Blood Hematopoietic Stem Cells, Mononuclear Cells and Granulocytes

GranulomaGranulomatous Disease, ChronicLeukocyte Disease+2 more
National Institute of Allergy and Infectious Diseases (NIAID)850 enrolled1 locationNCT00001405
Recruiting

Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset

Congenital MalformationRare Fetal Genetic Diseases
Assistance Publique - Hôpitaux de Paris63 enrolled1 locationNCT06475651
Recruiting
Phase 3

Evaluation of Efficacy and Safety of a Single Dose of CTX001 in Participants With Transfusion-Dependent β-Thalassemia and Severe Sickle Cell Disease

Beta-ThalassemiaSickle Cell DiseaseHematologic Diseases+4 more
Vertex Pharmaceuticals Incorporated26 enrolled6 locationsNCT05477563
Recruiting

Molecular Diagnosis of Systemic Autoinflammatory Diseases

Genetic DiseaseMolecular Pathway DeregulationSomatic Mutation+2 more
Institut National de la Santé Et de la Recherche Médicale, France300 enrolled1 locationNCT05364294
Recruiting

CUHK Stroke Biobank

Stroke, IschemicGenetic DiseaseAtherosclerosis, Cerebral
Chinese University of Hong Kong500 enrolled1 locationNCT03291392
Recruiting

Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome

Genetic DiseaseChopra-Amiel-Gordon SyndromeCAGS+1 more
Boston Children's Hospital125 enrolled1 locationNCT05528744
Recruiting

Natural History of Type 1 Interferonopathies: Insights From a European Cohort

Genetic DiseaseAutoimmune DiseasesNeurological Diseases or Conditions+1 more
Imagine Institute500 enrolled32 locationsNCT07040774
Recruiting

Accurate Assessment and Intervention Research on Newborn Whole Genome Sequencing and Genetic Disease Risk

Genetic Disease
Women's Hospital School Of Medicine Zhejiang University1,000,000 enrolled1 locationNCT07365254
Recruiting
Phase 3

A Study to Learn About the Safety and Efficacy of the Drug Oleogel-S10 in Japanese Patients With Epidermolysis Bullosa

Skin DiseasesEpidermolysis BullosaConnective Tissue Disease+7 more
Chiesi Farmaceutici S.p.A.6 enrolled6 locationsNCT06917690
Recruiting
Not Applicable

Biocollection of Rare Pediatric-onset of Autoimmune and Autoinflammatory Diseases

Genetic DiseaseAutoimmune DiseasesAutoinflammatory Disease+1 more
Hospices Civils de Lyon400 enrolled13 locationsNCT06435468
Recruiting
Not Applicable

Using a Speech-Generating Device to Support Communication in Childhood Dementia

Genetic DiseaseChildhood DementiaNonverbal Communication+1 more
Murdoch Childrens Research Institute38 enrolled1 locationNCT07039084
Recruiting

STXBP1 and SYNGAP1 Related Disorders Natural History Study

Genetic DiseaseSYNGAP1-Related Intellectual DisabilitySTXBP1 Encephalopathy With Epilepsy
Children's Hospital of Philadelphia600 enrolled5 locationsNCT06555965
Recruiting

Biobank Clinical Genetics Maastricht (KG01)

Genetic Disease
Maastricht University Medical Center3,600 enrolled1 locationNCT02266615
Recruiting

Genomic Sequencing and Personalized Treatment for Birth Defects in Neonatal Intensive Care Units

Genetic DiseaseMultiple MalformationCongenital Malformation
Children's Hospital of Fudan University2,000 enrolled1 locationNCT02551081
Recruiting

A Comparative Analysis of Speech Perception Between Cochlear Implant Patients and DFNB9 Patients Receiving Gene Therapy

Genetic DiseaseHearing LossSpeech Perception
Eye & ENT Hospital of Fudan University180 enrolled6 locationsNCT06237790
Recruiting

Follow-up With Preimplantation Genetic Testing Patients

InfertilityGenetic DiseaseIVF
Genomic Prediction Inc.10,000 enrolled1 locationNCT04477863
Recruiting
Phase 2

Rifampin in CYP24A1-related Hypercalcemia and Hypercalciuria

Genetic DiseaseIdiopathic Infantile Hypercalcaemia - Severe FormHypercalcemia, Idiopathic, of Infancy+3 more
Children's Hospital of Philadelphia60 enrolled1 locationNCT03301038