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NCT00600873 · ClinicalTrials.gov registry record · Phase 1
R(+)PPX High Dose Treatment of ALS
A Phase 1 study of Amyotrophic Lateral Sclerosis, sponsored by Bennett, James P., Jr., M.D., Ph.D..
- Completed
- Registry status
- Phase 1
- Development phase
- 10
- Enrollment target
- 1
- Study location
NCT00600873 is a Phase 1 study of Amyotrophic Lateral Sclerosis that has completed, run by Bennett, James P., Jr., M.D., Ph.D.. The registered enrollment target is 10 participants, below the 898-participant average among 102 other Amyotrophic Lateral Sclerosis trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00600873, a Phase 1 study of Amyotrophic Lateral Sclerosis, has completed, sponsored by Bennett, James P., Jr., M.D., Ph.D..
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 10 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Conditions Studied
Interventions
- DRUG R(+) pramipexole dihydrochloride monohydrate
Study Locations (1)
Virginia
- University of Virginia - Charlottesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2007-08 |
| Est. Completion | 2009-01 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00600873
The ClinicalTrials.gov registry entry for NCT00600873 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 898-participant average among 102 other Amyotrophic Lateral Sclerosis trials with a reported enrollment target (99% lower). The listed sponsor is Bennett, James P., Jr., M.D., Ph.D., which has 2 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Amyotrophic Lateral Sclerosis appearing as the primary indexed condition, and to 1 intervention - of which R(+) pramipexole dihydrochloride monohydrate is the first listed.
NCT00600873 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.
Frequently Asked Questions
What is clinical trial NCT00600873 about?
NCT00600873 is a clinical study titled "R(+)PPX High Dose Treatment of ALS". 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.
What is the current status of trial NCT00600873?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2007-08. Estimated completion is 2009-01.
What conditions does trial NCT00600873 study?
This clinical trial studies the following conditions: Amyotrophic Lateral Sclerosis.
What interventions are being tested in trial NCT00600873?
The interventions under investigation include: R(+) pramipexole dihydrochloride monohydrate (DRUG).
Who is sponsoring clinical trial NCT00600873?
This trial is sponsored by Bennett, James P., Jr., M.D., Ph.D., which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00600873 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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