Crick
HomeTrialsGenesDrugs23andMeGraphBlogContact
  • Home
  • Trials
  • Genes
  • Drugs
  • 23andMe
  • Graph
  • Blog
  • Contact
Crick

An open-source clinical intelligence platform. Explore clinical trials, gene networks, and molecular structures using public data sources.

Data Sources

  • ClinicalTrials.gov
  • OpenTargets
  • ClinVar
  • PubChem

Links

  • Contact
  • About
  • Privacy

© 2026 Crick. All rights reserved.

Crick is for educational purposes only. Not medical advice.

Results for “Rare Ataxia”

15 trials

Filters

Phase
Early Phase 1
Phase 1
Phase 2
Phase 3
Phase 4
Status
Recruiting
Active, Not Recruiting
Not Yet Recruiting
Completed
Enrolling by Invitation

Showing 15 of 15 results

Not applicableUnknownNCT04319796
What this trial is testing

European Registry on Rare Neurological Diseases

Who this might be right for
Rare Diseases
University Hospital Tuebingen 5,000
Early research (Phase 1)Looking for participantsNCT07180355
What this trial is testing

SGT-212 Gene Therapy in Friedreich's Ataxia

Who this might be right for
Friedreich's Ataxia (FA)
Solid Biosciences Inc. 10
Not applicableLooking for participantsNCT06016946
What this trial is testing

Friedreich Ataxia Global Clinical Consortium UNIFIED Natural History Study

Who this might be right for
Friedreich Ataxia
Friedreich's Ataxia Research Alliance 3,000
Not applicableStudy completedNCT04200664
What this trial is testing

Audiovestibular Function in Infratentorial Superficial Siderosis

Who this might be right for
SiderosisNeurological DisorderRare Diseases+2 more
University College, London 11
Not applicableUnknownNCT00951886
What this trial is testing

The Validity of Forced Expiratory Maneuvers in Ataxia Telangiectasia Studied Longitudinally

Who this might be right for
Ataxia Telangiectasia
Sheba Medical Center 28
Not applicableEnrolling By InvitationNCT03655223
What this trial is testing

Early Check: Expanded Screening in Newborns

Who this might be right for
Spinal Muscular AtrophyFragile X SyndromeFragile X - Premutation+182 more
RTI International 30,000
Not applicableLooking for participantsNCT04880356
What this trial is testing

Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.

Who this might be right for
Inherited DiseaseRare DiseasesMetabolic Disease+3 more
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta 100
Not applicableStudy completedNCT04653909
What this trial is testing

The Physiotherapy and Rehabilitation in Calfan Syndrome

Who this might be right for
CALFAN Syndrome
Hasan Kalyoncu University 1
Not applicableWithdrawnNCT06560346
What this trial is testing

Understanding the Natural History Early in the Course or Presentation of Friedreich Ataxia

Who this might be right for
Friedreich AtaxiaRare Diseases
Friedreich's Ataxia Research Alliance
Not applicableUnknownNCT02867969
What this trial is testing

Slowing Down Disease Progression in Premanifest SCA: a Piloting Interventional Exergame Trial

Who this might be right for
Spinocerebellar Ataxia
University Hospital Tuebingen 26
Testing effectiveness (Phase 2)WithdrawnNCT03761511
What this trial is testing

Study of the Efficacy and Safety of Nicotinamide in Patients With Friedreich Ataxia

Who this might be right for
Friedreich Ataxia
RWTH Aachen University
Not applicableStudy completedNCT02874911
What this trial is testing

Coordination Training With Complete Body Video Games in Children and Adults With Degenerative Ataxias

Who this might be right for
Spinocerebellar Ataxia
University Hospital Tuebingen 10
Not applicableLooking for participantsNCT01793168
What this trial is testing

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

Who this might be right for
Rare DisordersUndiagnosed DisordersDisorders of Unknown Prevalence+340 more
Sanford Health 20,000
Not applicableStudy completedNCT00004306
What this trial is testing

Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)

Who this might be right for
Hereditary Ataxia
Office of Rare Diseases (ORD) 18
Not applicableLooking for participantsNCT06065852
What this trial is testing

National Registry of Rare Kidney Diseases

Who this might be right for
Adenine Phosphoribosyltransferase DeficiencyAH AmyloidosisAHL Amyloidosis+81 more
UK Kidney Association 35,000