University of Virginia
Charlottesville, Virginia, 22908, United States
NCT Number: NCT00600873
R(+)pramipexole is administered in escalating doses to patients with early ALS. Plasma and spinal fluid levels of R(+)PPX are monitored, in addition to biochemical markers of oxidative stress.
Looking for future studies?
Notify Me30 year–80 year
All sexes
Interventional
Phase 1 / Phase 2
Charlottesville, Virginia, 22908, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
100 mg tid orally daily
Time frame: 6 months
Time frame: 6 months
Time frame: 6 months
Looking for future studies?
Notify MeBennett, James P., Jr., M.D., Ph.D.
Indiv
Pharmacokinetics and Nitrative-Oxidative Stress Pharmacodynamics in Amyotrophic Lateral Sclerosis Subjects Taking Daily High-Dose R(+) Pramipexole Dihydrochloride for Six Months
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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