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NCT01764737 · ClinicalTrials.gov registry record · Phase 1

Evaluation of Safety, Tolerability, and PK of VX15/2503 In Patients With MS

A Phase 1 study of Multiple Sclerosis, sponsored by Vaccinex.

Completed
Registry status
Phase 1
Development phase
50
Enrollment target
10
Study locations

NCT01764737 is a Phase 1 study of Multiple Sclerosis that has completed, run by Vaccinex. The registered enrollment target is 50 participants, below the 585-participant average among 315 other Multiple Sclerosis trials with a reported enrollment target (91% lower). The trial reports 10 study locations across 9 states.

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The verdict

NCT01764737, a Phase 1 study of Multiple Sclerosis, has completed, sponsored by Vaccinex.

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target
10
Study locations

Study Summary

The purpose of this study is to evaluate the safety and tolerability of IV administration of VX15/2503 in patients with multiple sclerosis. The escalation part of the study will determine the maximum tolerated dose (MTD) or the Maximum Administered Dose if no MTD is found.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG VX15/2503

Study Locations (10)

New York

  • MS Center of Northeastern NY/Empire Neurology - Latham
  • University of Rochester Medical Center - Rochester

Alabama

  • North Central Neurology Associates, PC - Cullman

Colorado

  • University of Colorado Hospital, Aschutz Inpatient Pavilion - Aurora

Indiana

  • Indiana University Health Neuroscience Center - Indianapolis

Kansas

  • University of Kansas Medical Center - Kansas City

Michigan

  • Wayne State University - University Health Center - Detroit

North Carolina

  • The Neurological Institute, PA - Charlotte

Ohio

  • The Cleveland Clinic Foundation - Cleveland

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2012-12
Est. Completion 2014-11
Phase Phase 1

Sponsor

Vaccinex

7 total trials

What the Registry Record Tells You About NCT01764737

The ClinicalTrials.gov registry entry for NCT01764737 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 585-participant average among 315 other Multiple Sclerosis trials with a reported enrollment target (91% lower). The listed sponsor is Vaccinex, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Multiple Sclerosis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT01764737 reports 10 study locations spanning 9 distinct geographic areas - top geographies include New York, Alabama, Colorado.

Frequently Asked Questions

What is clinical trial NCT01764737 about?

NCT01764737 is a clinical study titled "Evaluation of Safety, Tolerability, and PK of VX15/2503 In Patients With MS". The purpose of this study is to evaluate the safety and tolerability of IV administration of VX15/2503 in patients with multiple sclerosis. The escalation part of the study will determine the maximum tolerated dose (MTD) or the Maximum Administered Dose if no MTD is found.

What is the current status of trial NCT01764737?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2012-12. Estimated completion is 2014-11.

What conditions does trial NCT01764737 study?

This clinical trial studies the following conditions: Multiple Sclerosis.

What interventions are being tested in trial NCT01764737?

The interventions under investigation include: Placebo (DRUG), VX15/2503 (DRUG).

Who is sponsoring clinical trial NCT01764737?

This trial is sponsored by Vaccinex, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01764737 being conducted?

This trial has 10 study locations across Alabama, Colorado, Indiana, Kansas, Michigan. 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

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.