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Clinical trial condition

Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,619 public trials 2,162 recruiting studies
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Genetic Diseases, Inborn trial results

Completed

Dupilumab in Adolescent and Adult Skin of Color Participants: Open-label Moderate-to-severe Eczema Trial

NCT05590585

Conditions
Atopic Eczema, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +14 more
Locations
  • Total Skin & Beauty Dermatology Center Birmingham, Alabama, United States
  • The University Of Alabama At Birmingham Birmingham, Alabama, United States
  • C2 Research Center, LLC Montgomery, Alabama, United States
  • Center for Dermatology Clinical Research, inc. Fremont, California, United States
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Completed

A Study to Evaluate the Safety and Efficacy of K-321 Eye Drops After Descemetorhexis in Participants With Fuchs Endothelial Corneal Dystrophy (FECD)

NCT05795699

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Diseases, Corneal Dystrophies, Hereditary, +5 more
Locations
  • Keck Hospital of USC Los Angeles, California, United States
  • Macy Eye Center Los Angeles, California, United States
  • Jules Stein Eye Institute Los Angeles, California, United States
  • Byers Eye Institute at Stanford Palo Alto, California, United States
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Completed

SARC031: MEK Inhibitor Selumetinib (AZD6244) in Combination With the mTOR Inhibitor Sirolimus for Patients With Malignant Peripheral Nerve Sheath Tumors

NCT03433183

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fibrosarcoma, Genetic Diseases, Inborn, +22 more
Locations
  • Children's National Medical Center Washington D.C., District of Columbia, United States
  • Johns Hopkins University Baltimore, Maryland, United States
  • National Cancer Institute Bethesda, Maryland, United States
  • Dana Farber Cancer Institute Boston, Massachusetts, United States
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Completed

Study of a National Cohort of Adult Patients With Phenylketonuria

NCT01619722

Conditions
Amino Acid Metabolism, Inborn Errors, Bone Diseases, Bone Diseases, Metabolic, +15 more
Locations
  • CHRU-Hôpital Bretonneau - Service de Médecine Interne-Nutrition Tours, Centre-Val de Loire, France
  • CHU-ANGERS -Médecine Interne Angers, France
  • CHU_Service de Médecine Interne Nutrition A2-Hôpital du Haut Levèque Bordeaux, France
  • CHU du Morvan-Département de Pédiatrie et génétique médicale, Brest, France
View all 16 locations
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