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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.

12,633 public trials 2,161 recruiting studies
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Genetic Diseases, Inborn trial results

Completed

Characterizing the Upper Airway Manifestations in Primary Ciliary Dyskinesia and Primary Immunodeficiencies

NCT04919018

Conditions
Abnormalities, Multiple, Bronchial Diseases, Bronchiectasis, +20 more
Locations
  • Washington University in St. Louis St Louis, Missouri, United States
  • University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States
  • The Hospital for Sick Children Toronto, Ontario, Canada
  • McGill University Montreal, Quebec, Canada
View Trial Details
Completed

Sickle Cell Disease, Hemechip

NCT03948516

Conditions
Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +7 more
Locations
  • University of Nebraska Medical Center Omaha, Nebraska, United States
  • University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States
  • Case Western Reserve University Cleveland, Ohio, United States
  • University Hospitals Cleveland Medical Center Cleveland, Ohio, United States
View Trial Details
Completed

Defining the Genetic Etiology of Suppurative Lung Disease in Children and Adults

NCT04702243

Conditions
Abnormalities, Multiple, Bronchial Diseases, Bronchiectasis, +20 more
Locations
  • Stanford University Palo Alto, California, United States
  • Children's Hospital Colorado Aurora, Colorado, United States
  • National Heart, Lung and Blood Institute Bethesda, Maryland, United States
  • Washington University in St. Louis St Louis, Missouri, United States
View Trial Details
Completed

The Effects of CGMP in Children and Adults With PKU

NCT04076176

Conditions
Amino Acid Metabolism, Inborn Errors, Brain Diseases, Brain Diseases, Metabolic, +9 more
Locations
  • Rigshospitalet Copenhagen, Denmark
  • Bristol Royal Hospital for Children Bristol, Avon, United Kingdom
  • Birmingham Children's Hospital Birmingham, West Midlands, United Kingdom
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Completed

PTG-300 in Subjects With Hereditary Hemochromatosis

NCT04202965

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +7 more
Locations
  • Protagonist Investigational Site Fayetteville, Georgia, United States
  • Protagonist Investigational Site Bethesda, Maryland, United States
  • Protagonist Investigational Site Charlotte, North Carolina, United States
  • Protagonist Investigational Site Conroe, Texas, United States
View Trial Details
Completed

An Observational Study of Upadacitinib to Assess Change in Disease Activity in Canadian Adult Participants With Moderate-to-Severe Atopic Dermatitis Who Are Inadequate Responders To or Discontinuing Dupilumab

NCT05394792

Conditions
Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +9 more
Locations
  • Dermatology Research Institute - Blackfoot Trail /ID# 246344 Calgary, Alberta, Canada
  • Laser Rejuvenation Clinics Inc. /ID# 255303 Calgary, Alberta, Canada
  • Rejuvenation Dermatology Clinic Calgary North /ID# 255623 Calgary, Alberta, Canada
  • Rejuvenation Dermatology - Edmonton Downtown /ID# 246298 Edmonton, Alberta, Canada
View all 25 locations
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