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NCT02222948 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety of Vatelizumab in Patients With Relapsing-Remitting Multiple Sclerosis

A Phase 2 study, sponsored by Genzyme, a Sanofi Company.

Terminated
Registry status
Phase 2
Development phase
112
Enrollment target

NCT02222948 is a Phase 2 study that was terminated before completion, run by Genzyme, a Sanofi Company. The registered enrollment target is 112 participants.

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The verdict

NCT02222948, a Phase 2 study, was terminated before completion, sponsored by Genzyme, a Sanofi Company.

TERMINATED
Registry status
Phase 2
Development phase
112 participants
Enrollment target

Study Summary

Primary Objectives: * To assess the efficacy of vatelizumab compared to placebo as measured by a reduction in new contrast-enhancing lesions (CELs) in relapsing remitting multiple sclerosis (RRMS) patients. * To evaluate multiple doses of vatelizumab for a dose-response. Secondary Objectives: * To evaluate the safety and tolerability of vatelizumab compared to placebo. * To evaluate the pharmacokinetics (PK) of vatelizumab.

Interventions

  • DRUG Vatelizumab
  • DRUG Placebo (for Vatelizumab)

Trial Details

FieldValue
Enrollment Target 112 participants
Start Date 2014-09
Est. Completion 2016-07
Phase Phase 2

Sponsor

Genzyme, a Sanofi Company

196 total trials

What the Registry Record Tells You About NCT02222948

The ClinicalTrials.gov registry entry for NCT02222948 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 112 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Genzyme, a Sanofi Company, which has 196 total studies on file at ClinicalTrials.gov.

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

NCT02222948 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02222948 about?

NCT02222948 is a clinical study titled "Efficacy and Safety of Vatelizumab in Patients With Relapsing-Remitting Multiple Sclerosis". Primary Objectives: * To assess the efficacy of vatelizumab compared to placebo as measured by a reduction in new contrast-enhancing lesions (CELs) in relapsing remitting multiple sclerosis (RRMS) patients. * To evaluate multiple doses of vatelizumab for a dose-response. Secondary Objectives: * T...

What is the current status of trial NCT02222948?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 112 participants. The study started on 2014-09. Estimated completion is 2016-07.

What interventions are being tested in trial NCT02222948?

The interventions under investigation include: Vatelizumab (DRUG), Placebo (for Vatelizumab) (DRUG).

Who is sponsoring clinical trial NCT02222948?

This trial is sponsored by Genzyme, a Sanofi Company, which has 196 total clinical trials registered on ClinicalTrials.gov.

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.