Brain Diseases, Metabolic - 19 Studies Found

Completed : Bioequivalence Study of Two Nitisinone Formulations Compared to Orfadin
: Hereditary Tyrosinemia, Type I
: 2016-04-20
:
  • Drug: Nitisinone A single oral
Completed : Bioequivalence Study of Two Oral Nitisinone Formulations to Treat Hereditary Tyrosinemia (HT-1)
: Hereditary Tyrosinemia, Type I
: 2016-04-21
:
  • Drug: Nitisinone A single oral
Completed : Bioavailability Food-Effect Study of an Oral Nitisinone Formulation to Treat Hereditary Tyrosinemia (HT-1)
: Hereditary Tyrosinemia, Type I
: 2016-04-21
: Drug: Nitisinone A single oral dose of Nitisinone 10 mg Tablet will be administered.
Not yet recruiting : The Effectiveness of Kuvan in Amish PKU Patients
: Phenylketonuria
: 2016-01-26
:
  • Drug: saproterin dihydrochloride

Not yet recruiting : Trial of Dichloroacetate in Pyruvate Dehydrogenase Complex Deficiency:
: Pyruvate Dehydrogenase Complex Deficiency
: 2015-11-17
:
  • Drug: Dichloroacetate (DCA) Pa
Not yet recruiting : Simplified Diet Approach in Phenylketonuria
: Phenylketonuria
: 2015-09-17
: Behavioral: Dietary Protein Counting and Free Fruits and Vegetables Subjects will be educated on new sim
Recruiting : Intervention and Outcomes in Duarte Galactosemia
: Duarte Galactosemia
: 2015-08-06
Active, not recruiting : A Phase 3 Substudy to Evaluate Executive Function in Adults With PKU Who Are Participating in the Phase 3 Study, 165-302
: Phenylketonuria
: 2015-06-03
: Other: Administration of CANTAB and Subject Global Assessment At designated visits, subject will perform
Completed : Testing of Four Home Phenylalanine Monitoring Prototype Devices
: Phenylketonurias
: 2015-05-13
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