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NCT00110591 · ClinicalTrials.gov registry record · Phase 1
Safety and Tolerability of PRO 140 in HIV Uninfected Male Volunteers
A Phase 1 study, sponsored by CytoDyn.
- Completed
- Registry status
- Phase 1
- Development phase
- 20
- Enrollment target
NCT00110591: Completed Phase 1 study, sponsored by CytoDyn.
NCT00110591 is a Phase 1 study that has completed, run by CytoDyn. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00110591, a Phase 1 study, has completed, sponsored by CytoDyn.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 20 participants
- Enrollment target
Study Summary
The purpose of the study is to determine the safety and tolerability of PRO 140, an investigational anti-HIV drug, administered via intravenous infusion. Study hypothesis: Single intravenous doses of PRO 140 can be safely administered to humans and will result in measurable concentrations of the product in serum.
Interventions
- DRUG PRO 140
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2004-04-16 |
| Est. Completion | 2008-03-31 |
| Phase | Phase 1 |
What the finished NCT00110591 record still lists
NCT00110591 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).
The record links to 0 conditions, and to 1 intervention - of which PRO 140 is the first listed.
NCT00110591 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00110591 about?
NCT00110591 is a clinical study titled "Safety and Tolerability of PRO 140 in HIV Uninfected Male Volunteers". The purpose of the study is to determine the safety and tolerability of PRO 140, an investigational anti-HIV drug, administered via intravenous infusion. Study hypothesis: Single intravenous doses of PRO 140 can be safely administered to humans and will result in measurable concentrations of the pr...
What is the current status of trial NCT00110591?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2004-04-16. Estimated completion is 2008-03-31.
What interventions are being tested in trial NCT00110591?
The interventions under investigation include: PRO 140 (DRUG).
Who is sponsoring clinical trial NCT00110591?
This trial is sponsored by CytoDyn, which has 18 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00110591's enrollment target sits among peer trials
20 1629th of 2000 higher than 285 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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