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NCT05489393

CureDRPLA Global Patient Registry

Recruiting now Last updated 17 March 2026
What this trial tests

trial in DRPLA in 100 participants. Currently enrolling.

Timeline
1 March 2021
Primary endpoint
1 November 2031
1 November 2031

Quick facts

Lead sponsorCureDRPLA
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment100
Start date1 March 2021
Primary completion1 November 2031
Estimated completion1 November 2031
Sites1 location across United States

Conditions studied

Sponsor

CureDRPLA

Who can join

Adults 0 to 100, any sex, with DRPLA. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of the CureDRPLA Global Patient Registry is to establish a longitudinal database of patient-reported data on individuals affected with Dentatorubral-pallidoluysian atrophy (DRPLA) from anywhere in the world. The CureDRPLA Global Patient Registry will address patient needs by: * Expanding patient engagement by documenting quality of life outcomes. * Providing anonymized data to the DRPLA research community on patient experience with the disease and priorities for treatment. * Connecting DRPLA patients with opportunities to participate in clinical research.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Polyglutamine (PolyQ) Diseases: Navigating the Landscape of Neurodegeneration.
    Tenchov R, Sasso JM, Zhou QA. · · 2024 · cited 31× · PMID 38996083 · DOI 10.1021/acschemneuro.4c00184
  2. Establishing resources and increasing awareness to advance research on Dentatorubral-pallidoluysian atrophy toward a treatment: a patient organization perspective.
    Prades S, Compton A, Carroll JB. · · 2024 · PMID 38716233 · DOI 10.1177/26330040241249189

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05489393.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing