Status:

COMPLETED

CJD (Creutzfeldt-Jakob Disease) Quinacrine Study

Lead Sponsor:

University of California, San Francisco

Collaborating Sponsors:

National Institute on Aging (NIA)

Conditions:

Creutzfeldt-Jakob Disease

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

The purpose of this clinical trial is to determine the effectiveness of the medication quinacrine on survival in sporadic Creutzfeldt-Jakob disease (sCJD).

Detailed Description

Creutzfeldt-Jakob disease (CJD)is a rapidly progressive, invariably fatal and untreatable neurodegenerative disease with a mean duration of about eight months. Beyond the debilitating cognitive and mo...

Eligibility Criteria

Inclusion

  • Diagnosis of probable or definite sCJD: Definite--biopsy confirmed sCJD; Probable--a progressive dementia with either a typical EEG or a typical MRI consistent with sCJD, and at least two of the following clinical features: myoclonus, pyramidal or extrapyramidal signs, visual symptoms, cerebellar signs, akinetic mutism, other focal higher cortical neurologic signs (e.g. neglect, apraxia, aphasia)
  • 18 years of age or older
  • Able to swallow
  • Able to follow simple one-step commands
  • Have had a brain MRI within 6 months and an EEG within 3 months ruling out other etiologies such as masses, strokes, or non-convulsive status epilepticus
  • Consent to autopsy in the event of their death during or after the study

Exclusion

  • History of other significant or life-threatening disease, including: cancer; end-stage liver or renal disease; severe heart disease
  • History of other disease requiring regular supportive care
  • Liver disease
  • Active alcoholism
  • Bone marrow suppression
  • Severe hypotension
  • Severe psoriasis
  • Poorly controlled diabetes
  • Women who are pregnant or breast-feeding
  • Men, or women of childbearing age, not practicing reliable contraception
  • Serious allergies to quinacrine or other acridines
  • Current or recent use of quinacrine (within 6 months)
  • \< 18 years of age
  • Any other contraindication to taking quinacrine
  • Genetic form of prion disease is identified prior to study enrollment
  • Current use of anti-arrhythmics (at discretion of investigator)
  • G6PD (Glucose 6-Phosphate Dehydrogenase) deficiency (at discretion of investigator)

Key Trial Info

Start Date :

April 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2012

Estimated Enrollment :

69 Patients enrolled

Trial Details

Trial ID

NCT00183092

Start Date

April 1 2005

End Date

June 1 2012

Last Update

June 9 2014

Active Locations (1)

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1

University of California, San Francisco

San Francisco, California, United States, 94143