Medical specialists from Belgium tagged as investigators in clinical trials studying Metabolism, Inborn Errors

Total 16 results

Aurélie Empain, M.D., Ph.D.
Seen in:
- Brussels, Hôpital Universitaire des enfants Reine Fabiola (HUDERF-ULB)
Trials:
- NCT06360913 (Principal Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Caroline Dadoumont, MD
Seen in:
- Liège, CHU Liege
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Céline Morelli, M.D.
Seen in:
- Brussels, Hôpital Universitaire des enfants Reine Fabiola (HUDERF-ULB)
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Corinne De Laet, M.D., Ph.D.
Seen in:
- Brussels, Hôpital Universitaire des enfants Reine Fabiola (HUDERF-ULB)
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Damien Lederer, M.D., Ph.D.
Seen in:
- Charleroi, Institut de Pathologie et de Génétique (IPG)
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Dominique Roland, M.D.
Seen in:
- Charleroi, Institut de Pathologie et de Génétique (IPG)
Trials:
- NCT06360913 (Principal Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Ebru Surgun, M.D.
Seen in:
- Brussels, Hôpital Universitaire des enfants Reine Fabiola (HUDERF-ULB)
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
François Boemer, Pharm D PhD
Seen in:
- Liège, CHU Liege
Trials:
- NCT06360913 (Principal Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
François-Guillaume Debray, MD PhD
Seen in:
- Liège, CHU Liege
Trials:
- NCT06360913 (Principal Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Isabelle Maystadt, M.D., Ph.D.
Seen in:
- Charleroi, Institut de Pathologie et de Génétique (IPG)
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Joseph P. Dewulf, M.D., Ph.D.
Seen in:
- Brussels, Cliniques Universitaires Saint Luc
Trials:
- NCT06360913 (Principal Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Lionel Marcélis, MSc, Ph.D.
Seen in:
- Brussels, Hôpital Universitaire des enfants Reine Fabiola (HUDERF-ULB)
Trials:
- NCT06360913 (Principal Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Marie-Cécile Nassogne, M.D., Ph.D.
Seen in:
- Brussels, Cliniques Universitaires Saint Luc
Trials:
- NCT06360913 (Principal Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Nicole Revencu, M.D., Ph.D.
Seen in:
- Brussels, Cliniques Universitaires Saint Luc
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Stéphanie Paquay, M.D.
Seen in:
- Brussels, Cliniques Universitaires Saint Luc
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism
Xavier Stephenne, M.D., Ph.D.
Seen in:
- Brussels, Cliniques Universitaires Saint Luc
Trials:
- NCT06360913 (Sub-Investigator)
Conditions:
- Rare Diseases;
- Inborn Errors of Metabolism

Clinical Trials on Metabolism, Inborn Errors

Sciotec Diagnostic Technologies GmbH

Not yet recruiting

Observational Study on the Safety and Efficacy of the Medical Product Fructosin.

Fructose Intolerance

Austria
Augusta University
University of Iowa; Teikyo University

Recruiting

Investigation of Alanine in Fructose Intolerance: A Dose Ranging Study

Fructose Intolerance

United States
Augusta University

Unknown

Investigation of Supplemental L-alanine in the Management of Dietary Fructose Intolerance

Fructose Intolerance

United States
University of Lausanne

Completed

Metabolic Consequences of Heterozygous Hereditary Fructose Intolerance

Glucose Metabolism Disorders | Fructose Metabolism, Inborn Errors | Hereditary Fructose Intolerance
Mayo Clinic
National Institute of Neurological Disorders and Stroke (NINDS)

Enrolling by invitation

Large-Scale Metabolomic Profiling for the Diagnosis of Inborn Errors of Metabolism

Congenital Disorders of Glycosylation

United States
Maastricht University Medical Center
Pfizer

Completed

Ketohexokinase Inhibition in Hereditary Fructose Intolerance (KHKi in HFI)

HFI

Netherlands
Augusta University

Terminated

Randomized Control Trial of L-Alanine and Placebo in Fructose Intolerance

Dietary Fructose Intolerance

United States
University of Lausanne
University of Liege

Completed

Fructose Supplementation in Carriers for Hereditary Fructose Intolerance

Hereditary Fructose Intolerance

Belgium
University of Miami
HRSA/Maternal and Child Health Bureau

Completed

The Early History of Universal Screening for Metabolic Disorders

Phenylketonuria | Inborn Errors of Metabolism | Galactosemia

United States
Orpha Labs

Completed

Study of ORL-1B in Patients With Biotinidase Deficiency

Biotinidase Deficiency

Medical specialists from Belgium tagged as investigators in clinical trials studying Metabolism, Inborn Errors

Clinical Trials on Metabolism, Inborn Errors

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CROs in Myanmar

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Rare Diseases

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