Page 1 of Clinical Trials for "Carbamoyl-Phosphate Synthase I Deficiency Disease", 428 Total Matches
- 1RecruitingLast Updated: January 25, 2012Condition(s): Urea Cycle Disorders; Carbamoylphosphate Synthetase I Deficiency Disease; Ornithine Transcarbamylase Deficiency Disease; Citrullinemia
- 2CompletedLast Updated: July 31, 2009Condition(s): Gaucher Disease Type I; Cerebroside Lipidosis Syndrome; Clucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form
- 3RecruitingLast Updated: December 8, 2011Condition(s): Gaucher Disease; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease
- 4Active, not recruitingLast Updated: December 16, 2011Condition(s): Gaucher Disease, Type 1; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form
- 5CompletedLast Updated: September 3, 2009Condition(s): Gaucher Disease, Type 1; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form
- 6CompletedLast Updated: June 29, 2009Condition(s): T-Cell Immune Deficiency Diseases; Severe Combined Immunodeficiency
- 7Not yet recruitingLast Updated: May 14, 2012Condition(s): Propionic Acidemia (PA); Methylmalonic Acidemia (MMA); Late-onset CPS1 Deficiency (CPSD); Late-onset Ornithine Transcarbamylase Deficiency (OTCD)
- 8Not yet recruitingLast Updated: October 6, 2006Condition(s): Deficiency Diseases
- 9CompletedLast Updated: March 3, 2008Condition(s): Healthy; Deficiency Disease
- 10SuspendedLast Updated: February 6, 2009Condition(s): Canavan Disease; Infantile; Deficiency Disease; Aspartoacylase; Leukodystrophy, Spongiform
- 11RecruitingLast Updated: December 6, 2011Condition(s): Urea Cycle Disorders, Inborn; Inborn Errors of Metabolism; Propionic Acidemia; Methylmalonic Acidemia; Carbamyl Phosphate Synthetase Deficiency
- 12TerminatedPhase I Pilot Study of Liver-Directed Gene Therapy for Partial Ornithine Transcarbamylase DeficiencyLast Updated: June 23, 2005Condition(s): Ornithine Transcarbamylase Deficiency Disease
- 13Active, not recruitingLast Updated: June 23, 2005Condition(s): Ornithine Transcarbamylase Deficiency Disease
- 14CompletedLast Updated: June 24, 2010Condition(s): Pompe Disease (Late-onset); Glycogen Storage Disease Type II (GSD-II); Acid Maltase Deficiency Disease; Glycogenosis 2
- 15CompletedLast Updated: July 6, 2009Condition(s): Glycogen Storage Disease Type II; Pompe Disease; Acid Maltase Deficiency Disease; Glycogenosis 2
- 16CompletedLast Updated: July 7, 2009Condition(s): Pompe Disease (Late-Onset); Glycogen Storage Disease Type II (GSD-II); Acid Maltase Deficiency Disease; Glycogenosis 2
- 17Approved for marketingLast Updated: October 25, 2010Condition(s): Glycogen Storage Disease Type II (GSD-II); Pompe Disease (Late-onset); Acid Maltase Deficiency Disease; Glycogenosis 2
- 18CompletedLast Updated: July 7, 2009Condition(s): Pompe Disease (Late-Onset); Glycogen Storage Disease Type II (GSD-II); Acid Maltase Deficiency Disease; Glycogenosis 2
- 19CompletedLast Updated: March 14, 2011Condition(s): Glycogen Storage Disease Type II; Pompe Disease; Acid Maltase Deficiency Disease; Glycogenosis 2
- 20RecruitingLast Updated: May 4, 2012Condition(s): Pompe Disease; Glycogen Storage Disease Type II (GSD-II); Acid Maltase Deficiency Disease
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Carbamoyl-Phosphate+Synthase+I+Deficiency+Disease%22
