Friedrich-Baur Institut
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 6 Trials 
10 Trials

   

 
Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Klopstock, Thomas
NCT04604548: The KHENEREXT Study

Completed
2
11
Europe
Oral administration of 100 mg KH176 twice daily
Khondrion BV, Julius Clinical, ProPharma Group, Certara
Mitochondrial Diseases, Mitochondrial DNA tRNALeu(UUR) m.3243A
06/23
06/23
STRIDE, NCT04535609 / 2020-002855-40: An Efficacy and Safety Study of 24 Week Treatment With Mavodelpar (REN001) in Primary Mitochondrial Myopathy Patients

Completed
2
213
Europe, Canada, US, RoW
Mavodelpar, REN001, Placebo
Reneo Pharma Ltd
Primary Mitochondrial Myopathy
09/23
10/23
PMD-OPTION, NCT05972954 / 2022-003307-16: OMT-28 in Patients With Primary Mitochondrial Disease (PMD)

Active, not recruiting
2
32
Europe
OMT-28
Omeicos Therapeutics GmbH, OMEICOS Therapeutics GmbH
Primary Mitochondrial Disease
03/25
06/25
PROFA, NCT05943002: Patient-reported, Health Economic and Psychosocial Outcomes in Friedreich Ataxia

Recruiting
N/A
200
Europe
German Center for Neurodegenerative Diseases (DZNE), McMaster University, Sorbonne University
Friedreich Ataxia
08/24
10/24
EFACTS, NCT02069509: Patient Registry of the European Friedreich's Ataxia Consortium for Translational Studies

Recruiting
N/A
1200
Europe, RoW
European Friedreich's Ataxia Consortium for Translational Studies
Friedreich's Ataxia
12/24
12/24
SPORTAX-NHS, NCT02701036: Sporadic Degenerative Ataxia With Adult Onset: Natural History Study

Recruiting
N/A
300
Europe
Ataxia Study Group, German Center for Neurodegenerative Diseases (DZNE)
Late Onset Sporadic Cerebellar Ataxia
12/30
12/30
HSP-PBP, NCT03981276: Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related Disorders

Recruiting
N/A
2000
Europe
Clinical rating scale to measure disease severity and progression, Spastic Paraplegia Rating Scale (SPRS), Next-Gen Sequencing (NGS)
Dr. Rebecca Schule, German Federal Ministry of Education and Research, German Center for Neurodegenerative Diseases (DZNE)
Hereditary Spastic Paraplegia
08/39
08/41
UNIFAI, NCT06016946: Friedreich Ataxia Global Clinical Consortium UNIFIED Natural History Study

Recruiting
N/A
3000
Europe, Canada, US, RoW
Friedreich's Ataxia Research Alliance
Friedreich Ataxia
01/48
01/48
NCT05554835: Global Registry and Natural History Study for Mitochondrial Disorders

Recruiting
N/A
6000
Europe
LMU Klinikum, European Commission, German Federal Ministry of Education and Research, University of Pisa
Mitochondrial Diseases, Kearns-Sayre Syndrome, MIDD, SANDO, SCAE, NARP Syndrome, MELAS Syndrome, MERRF Syndrome, Coenzyme Q10 Deficiency, LHON, MNGIE, MIRAS, Barth Syndrome, MDS, Mitochondrial Myopathies, Leigh Syndrome, Pearson Syndrome, CPEO
12/40
12/40
TIRCON, NCT05522374: International NBIA Registry

Recruiting
N/A
2000
Europe, Canada, RoW
LMU Klinikum, Seventh Framework Programme, NBIA Alliance
Neurodegeneration With Brain Iron Accumulation (NBIA), Pantothenate Kinase-associated Neurodegeneration (PKAN), Beta-Propeller Protein-Associated Neurodegeneration (BPAN), Mitochondrial Membrane Protein Associated Neurodegeneration (MPAN), Fatty Acid Hydroxylase-associated Neurodegeneration (FAHN), Kufor Rakeb Syndrome, Neuroferritinopathy, Aceruloplasminemia, Woodhouse Sakati Syndrome, COASY Protein-associated Neurodegeneration (CoPAN), PLA2G6-Associated Neurodegeneration (PLAN)
12/40
12/40

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