Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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.

View on ClinicalTrials.gov ↗

View your shortlist →

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

FieldValue
Enrollment Target 88 participants
Start Date 2003-05
Est. Completion 2004-11
Phase Phase 2
Biosynexus Incorporated

4 total trials

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.

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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03843463 · 88 participants · Phase 2

    Escitalopram and Language Intervention for Subacute Aphasia

  • NCT04066348 · 88 participants · Phase 2

    TNF-α Treatment of Blast-Induced Tinnitus

  • NCT04331704 · 88 participants · Phase 4

    ANCHORS Alcohol & Sexual Health Study: UH3 Project

  • NCT04536103 · 88 participants

    Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00631800, the US trial registry maintained by the National Library of Medicine. NCT00631800 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.