Oroticaciduria 1: Clinical Trials

2 trials for Oroticaciduria 1, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

1 completed, 1 recruiting. 1 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 31Completed 1

Follow Oroticaciduria 1: new trials by email Literature Review of Oroticaciduria 1 trials Research Report on Oroticaciduria 1

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders
AMPD3, OMIM*102772, AMP Deaminase Deficiency, AK1, OMIM *103000, Adenylate Kinase Deficiency
RecruitingNational Human Genome Research Institute (NHGRI)9992023-12-192026-08-19
Open-Label Study of Uridine Triacetate in Pediatric Patients With Hereditary Orotic Aciduria
uridine triacetate - Hereditary Orotic Aciduria
Phase 3CompletedWellstat Therapeutics42014-04-012017-07-31

Narrower conditions

ADA2 protein, human (1)  ·  Adenine phosphoribosyltransferase deficiency (1)  ·  Adenosine monophosphate deaminase deficiency (1)  ·  Adenylosuccinate lyase deficiency (1)  ·  Anemia (1)  ·  Arts syndrome (1)  ·  Beta-Ureidopropionase Deficiency (1)  ·  Charcot-Marie-Tooth Disease (1)  ·  Dihydropyrimidinase Deficiency (1)  ·  Dihydropyrimidine Dehydrogenase Deficiency (1)  ·  Genee-Wiedemann syndrome (1)  ·  Hemolysis (1)  ·  Hyper-IgM Immunodeficiency Syndrome (1)  ·  Inosine Triphosphatase Deficiency (1)

Broader conditions

Blood Protein Disorders (1)  ·  Brain Diseases (1)  ·  Brain Diseases, Metabolic (1)  ·  Brain Diseases, Metabolic, Inborn (1)  ·  Cardiovascular Diseases (1)  ·  Central Nervous System Diseases (1)  ·  Cerebrovascular Disorders (1)  ·  Congenital Abnormalities (1)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1)  ·  Dysgammaglobulinemia (1)  ·  Genetic Diseases, Inborn (1)  ·  Genetic Diseases, X-Linked (1)  ·  Hematologic Diseases (1)  ·  Hemic and Lymphatic Diseases (1)  ·  Hereditary Sensory and Motor Neuropathy (1)

Interventions

uridine triacetate (1)

Sponsors

National Human Genome Research Institute (NHGRI) (1)  ·  Wellstat Therapeutics (1)

Countries

United States (2)

Top investigators

Michael K. Bamat, Ph.D. (1)  ·  Oleg A Shchelochkov, M.D. (1)