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NCT01492374 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Safety, Tolerability and the Effect of BMS-241027 on Cerebrospinal Fluid Biomarkers in Subjects With Mild Alzheimer's Disease

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

Completed
Registry status
Phase 1
Development phase
40
Enrollment target

NCT01492374 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 40 participants.

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The verdict

NCT01492374, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

The purpose of the study is to evaluate safety and the pharmacodynamic effects of BMS-241027 on cerebrospinal fluid (CSF) Tau, connectivity magnetic resonance imaging (MRI), and computerized cognitive tests in mild Alzheimer's disease (AD) subjects, following 9 weekly intravenous (IV) infusions of BMS-241027

Interventions

  • DRUG BMS-241027
  • DRUG Placebo matching BMS-241027

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2012-02
Est. Completion 2013-10
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT01492374

The ClinicalTrials.gov registry entry for NCT01492374 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which BMS-241027 is the first listed.

NCT01492374 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01492374 about?

NCT01492374 is a clinical study titled "Study to Evaluate the Safety, Tolerability and the Effect of BMS-241027 on Cerebrospinal Fluid Biomarkers in Subjects With Mild Alzheimer's Disease". The purpose of the study is to evaluate safety and the pharmacodynamic effects of BMS-241027 on cerebrospinal fluid (CSF) Tau, connectivity magnetic resonance imaging (MRI), and computerized cognitive tests in mild Alzheimer's disease (AD) subjects, following 9 weekly intravenous (IV) infusions of B...

What is the current status of trial NCT01492374?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2012-02. Estimated completion is 2013-10.

What interventions are being tested in trial NCT01492374?

The interventions under investigation include: BMS-241027 (DRUG), Placebo matching BMS-241027 (DRUG).

Who is sponsoring clinical trial NCT01492374?

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

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

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.