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NCT01963611 · ClinicalTrials.gov registry record · Phase 2

Efficacy, Safety, and Tolerability of Plovamer Acetate (Pathway 1)

A Phase 2 study, sponsored by EMD Serono.

Terminated
Registry status
Phase 2
Development phase
255
Enrollment target

NCT01963611 is a Phase 2 study that was terminated before completion, run by EMD Serono. The registered enrollment target is 255 participants.

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The verdict

NCT01963611, a Phase 2 study, was terminated before completion, sponsored by EMD Serono.

TERMINATED
Registry status
Phase 2
Development phase
255 participants
Enrollment target

Study Summary

This is a Phase 2, randomized, rater-blinded, 5-arm, parallel-group trial that will test 4 doses of plovamer acetate against the active comparator Copaxone in subjects with Relapsing Remitting Multiple Sclerosis (RRMS). The trial will be conducted on an outpatient basis for minimum treatment duration of 40 weeks.

Interventions

  • DRUG Plovamer acetate 0.5 milligram (mg)
  • DRUG Copaxone 20 mg
  • DRUG Plovamer acetate 3 mg
  • DRUG Plovamer acetate 10 mg
  • DRUG Plovamer acetate 20 mg

Trial Details

FieldValue
Enrollment Target 255 participants
Start Date 2013-10
Est. Completion 2015-03
Phase Phase 2

Sponsor

EMD Serono

71 total trials

What the Registry Record Tells You About NCT01963611

The ClinicalTrials.gov registry entry for NCT01963611 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 255 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is EMD Serono, which has 71 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Plovamer acetate 0.5 milligram (mg) is the first listed.

NCT01963611 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01963611 about?

NCT01963611 is a clinical study titled "Efficacy, Safety, and Tolerability of Plovamer Acetate (Pathway 1)". This is a Phase 2, randomized, rater-blinded, 5-arm, parallel-group trial that will test 4 doses of plovamer acetate against the active comparator Copaxone in subjects with Relapsing Remitting Multiple Sclerosis (RRMS). The trial will be conducted on an outpatient basis for minimum treatment duratio...

What is the current status of trial NCT01963611?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 255 participants. The study started on 2013-10. Estimated completion is 2015-03.

What interventions are being tested in trial NCT01963611?

The interventions under investigation include: Plovamer acetate 0.5 milligram (mg) (DRUG), Copaxone 20 mg (DRUG), Plovamer acetate 3 mg (DRUG), Plovamer acetate 10 mg (DRUG), Plovamer acetate 20 mg (DRUG).

Who is sponsoring clinical trial NCT01963611?

This trial is sponsored by EMD Serono, which has 71 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.