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Lipid Metabolism, Inborn Errors

Clinical trial condition

Lipid Metabolism, Inborn Errors

Explore clinical trials studying Lipid Metabolism, Inborn Errors. Study availability and eligibility vary by location and protocol.

833 public trials 155 recruiting studies

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Lipid Metabolism, Inborn Errors trial results

Completed

Study To Evaluate The Effect Of Torcetrapib/Atorvastatin In Patients With Genetic High Cholesterol Disorder

NCT00134511

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
Locations: Pfizer Investigational Site Boston, Massachusetts, United States

Pfizer Investigational Site Chicoutimi, Quebec, Canada

Pfizer Investigational Site Ste-Foy, Quebec, Canada

Pfizer Investigational Site Parktown, Johannesburg, South Africa

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Completed

Study To Evaluate The Safety And Efficacy Of Torcetrapib/Atorvastatin In Subjects With Familial Hypercholerolemia

NCT00134485

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +10 more
Locations: Pfizer Investigational Site San Diego, California, United States

Pfizer Investigational Site Washington D.C., District of Columbia, United States

Pfizer Investigational Site Lutz, Florida, United States

Pfizer Investigational Site Tampa, Florida, United States

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Completed

Prenatal Screening For Smith-Lemli-Opitz Syndrome

NCT00070850

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Foundation for Blood Research Scarborough, Maine, United States

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Completed

Phase I Single Dose-Escalation Safety Study of Human Glucocerebrosidase (prGCD)

NCT00258778

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +14 more
Locations: Not specified

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Completed

Efficacy Study of Extended-Release Niacin/Lovastatin Versus Usual Care

NCT00345657

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemia, Dyslipidemias, +11 more
Locations: Family Medical Care of Tulsa Tulsa, Oklahoma, United States

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Completed

Stem Cell Transplantation (SCT) for Genetic Diseases

NCT00004378

Conditions: Anemia, Anemia, Aplastic, Anemia, Diamond-Blackfan, +47 more
Locations: University of California Los Angeles Medical Center Los Angeles, California, United States

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Completed

Phase I Study of Retrovirally Mediated Transfer of the Human Glucocerebrosidase Gene Into Peripheral Blood Stem Cells for Autologous Transplantation in Patients With Type I Gaucher Disease

NCT00004294

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: University of Pittsburgh Pittsburgh, Pennsylvania, United States

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Completed

Phase II Pilot Study of Granulocyte Colony-Stimulating Factor for Inherited Bone Marrow Failure Syndromes

NCT00004787

Conditions: Anemia, Anemia, Aplastic, Anemia, Hypoplastic, Congenital, +34 more
Locations: Not specified

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Completed

Phase I Study of Ex Vivo Liver-Directed Gene Therapy for Familial Hypercholesterolemia

NCT00004809

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Dyslipidemias, +13 more
Locations: Not specified

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Completed

Diagnostic and Screening Study of Genetic Disorders

NCT00006057

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +25 more
Locations: Mount Sinai School of Medicine New York, United States

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Lipid Metabolism, Inborn Errors

Lipid Metabolism, Inborn Errors trial results

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