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NCT00277225 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Pharmacokinetics, Immunogenicity and Safety of Escalating Doses of BMS-188667 Given as a Single Intravenous Infusion to Patients With Psoriasis Vulgaris

A Phase 1 study of Psoriasis Vulgaris, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
32
Enrollment target
1
Study location

NCT00277225 is a Phase 1 study of Psoriasis Vulgaris that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 32 participants, below the 87-participant average among 6 other Psoriasis Vulgaris trials with a reported enrollment target (63% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00277225, a Phase 1 study of Psoriasis Vulgaris, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
32 participants
Enrollment target
1
Study location

Study Summary

The purpose of this protocol is to determine the single-dose pharmacokinetics and immunogicity of BMS-188667 administered as a 1 hour intravenous infusion with extended pharmacokinetic sampling. Safety of all subjects will be assessed in a double blind fashion through the inclusion of placebo controls at each dose level.

Conditions Studied

Interventions

  • DRUG Abatacept

Study Locations (1)

California

  • California Clinical Trials Medical Group - Beverly Hills

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 1995-11
Est. Completion 1996-06
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT00277225

The ClinicalTrials.gov registry entry for NCT00277225 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 87-participant average among 6 other Psoriasis Vulgaris trials with a reported enrollment target (63% lower). The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Psoriasis Vulgaris appearing as the primary indexed condition, and to 1 intervention - of which Abatacept is the first listed.

NCT00277225 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT00277225 about?

NCT00277225 is a clinical study titled "A Study to Assess the Pharmacokinetics, Immunogenicity and Safety of Escalating Doses of BMS-188667 Given as a Single Intravenous Infusion to Patients With Psoriasis Vulgaris". The purpose of this protocol is to determine the single-dose pharmacokinetics and immunogicity of BMS-188667 administered as a 1 hour intravenous infusion with extended pharmacokinetic sampling. Safety of all subjects will be assessed in a double blind fashion through the inclusion of placebo contro...

What is the current status of trial NCT00277225?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 1995-11. Estimated completion is 1996-06.

What conditions does trial NCT00277225 study?

This clinical trial studies the following conditions: Psoriasis Vulgaris.

What interventions are being tested in trial NCT00277225?

The interventions under investigation include: Abatacept (DRUG).

Who is sponsoring clinical trial NCT00277225?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00277225 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.