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NCT00631800 · ClinicalTrials.gov registry record · Phase 2
Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity Study in VLBW Neonates of BSYX-A110
A Phase 2 study, sponsored by Biosynexus Incorporated.
- Completed
- Registry status
- Phase 2
- Development phase
- 88
- Enrollment target
NCT00631800: Completed Phase 2 study, sponsored by Biosynexus Incorporated.
NCT00631800 is a Phase 2 study that has completed, run by Biosynexus Incorporated. The registered enrollment target is 88 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (34% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00631800, a Phase 2 study, has completed, sponsored by Biosynexus Incorporated.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 88 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety (including tolerability), pharmacokinetics, pharmacodynamics and clinical activity of BSYX-A110 administered in a 3-dose regimen on Study Days 0, 7, and 14.
Interventions
- DRUG Pagibaximab (formerly BSYX-A110)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2003-05 |
| Est. Completion | 2004-11 |
| Phase | Phase 2 |
What the finished NCT00631800 record still lists
NCT00631800 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 88 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (34% lower).
The record links to 0 conditions, and to 1 intervention - of which Pagibaximab (formerly BSYX-A110) is the first listed.
NCT00631800 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00631800 about?
NCT00631800 is a clinical study titled "Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity Study in VLBW Neonates of BSYX-A110". The purpose of this study is to evaluate the safety (including tolerability), pharmacokinetics, pharmacodynamics and clinical activity of BSYX-A110 administered in a 3-dose regimen on Study Days 0, 7, and 14.
What is the current status of trial NCT00631800?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 88 participants. The study started on 2003-05. Estimated completion is 2004-11.
What interventions are being tested in trial NCT00631800?
The interventions under investigation include: Pagibaximab (formerly BSYX-A110) (DRUG).
Who is sponsoring clinical trial NCT00631800?
This trial is sponsored by Biosynexus Incorporated, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00631800's enrollment target sits among peer trials
88 803rd of 2000 higher than 1,191 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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