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
  • Privacy

© 2026 Crick. All rights reserved.

Crick is for educational purposes only. Not medical advice.

Results for “Allan-Herndon-Dudley Syndrome”

11 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 11 of 11 results

Large-scale testing (Phase 3)UnknownNCT05019417
What this trial is testing

Glycerol-Phenylbutyrate Treatment in Children With MCT Mutation (Allan-Herndon- Dudley Syndrome)

Who this might be right for
Monocarboxylate Transporter 8 Deficiency
Kaplan Medical Center 6
Not applicableAvailableNCT05911399
What this trial is testing

Expanded Access Program for Tiratricol in Patients With Monocarboxylate Transporter 8 Deficiency

Who this might be right for
Monocarboxylate Transporter 8 DeficiencyAllan-Herndon-Dudley Syndrome
Rare Thyroid Therapeutics International AB
Testing effectiveness (Phase 2)Study completedNCT02060474
What this trial is testing

Thyroid Hormone Analog Therapy in MCT8 Deficiency: Triac Trial Patients

Who this might be right for
Allan-Herndon-Dudley Syndrome
Erasmus Medical Center 46
Not applicableAvailableNCT04143295
What this trial is testing

Rescue of Infants With MCT8 Deficiency

Who this might be right for
Mct8 (Slc16A2)-Specific Thyroid Hormone Cell Transporter Deficiency
Roy E. Weiss, M.D.
Not applicableLooking for participantsNCT06566066
What this trial is testing

Register for Patients With Thyroid Hormone Resistance.

Who this might be right for
HypothyroidismGlobal Developmental DelayIntellectual Disability+5 more
Charite University, Berlin, Germany 200
Testing effectiveness (Phase 2)Active Not RecruitingNCT02396459
What this trial is testing

Triac Trial II in MCT8 Deficiency Patients

Who this might be right for
Allan-Herndon-Dudley Syndrome
Rare Thyroid Therapeutics International AB 22
Large-scale testing (Phase 3)Study completedNCT05579327
What this trial is testing

Withdrawal of Tiratricol Treatment in Males With Monocarboxylate Transporter 8 Deficiency (MCT8 Deficiency)

Who this might be right for
Monocarboxylate Transporter 8 DeficiencyAllan-Herndon-Dudley Syndrome
Rare Thyroid Therapeutics International AB 20
Not applicableStudy completedNCT06060197
What this trial is testing

MCT8 Deficiency Caregiver Study

Who this might be right for
Monocarboxylate Transporter 8 (MCT8) DeficiencyAllan-Herndon-Dudley Syndrome
Rare Thyroid Therapeutics International AB 21
Not applicableLooking for participantsNCT03047369
What this trial is testing

The Myelin Disorders Biorepository Project

Who this might be right for
LeukodystrophyWhite Matter DiseaseLeukoencephalopathies+63 more
Children's Hospital of Philadelphia 12,000
Not applicableLooking for participantsNCT04463316
What this trial is testing

GROWing Up With Rare GENEtic Syndromes

Who this might be right for
Prader-Willi SyndromePWS-like SyndromeSilver Russel Syndrome+30 more
dr. Laura C. G. de Graaff-Herder 600
Not applicableStudy completedNCT02699190
What this trial is testing

LeukoSEQ: Whole Genome Sequencing as a First-Line Diagnostic Tool for Leukodystrophies

Who this might be right for
LeukodystrophyWhite Matter Disease4H Syndrome+61 more
Children's Hospital of Philadelphia 236