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NCT01662908 · ClinicalTrials.gov registry record · Phase 2

A Randomized, Open-Label, Parallel-Group, Multi-Center Study for the Evaluation of Efficacy and Safety of Edoxaban Monotherapy Versus Low Molecular Weight (LMW) Heparin/Warfarin in Subjects With Symptomatic Deep-Vein Thrombosis

A Phase 2 study, sponsored by Daiichi Sankyo.

Completed
Registry status
Phase 2
Development phase
85
Enrollment target

NCT01662908 is a Phase 2 study that has completed, run by Daiichi Sankyo. The registered enrollment target is 85 participants.

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The verdict

NCT01662908, a Phase 2 study, has completed, sponsored by Daiichi Sankyo.

COMPLETED
Registry status
Phase 2
Development phase
85 participants
Enrollment target

Study Summary

Assess the relative change in thrombus volume as determined by two assessments (Baseline and Day 14-21) with magnetic resonance venography (MRV) in subjects with deep-vein thrombosis (DVT) treated with either an edoxaban monotherapy regimen or a low molecular weight (LMW) heparin/warfarin regimen.

Interventions

  • DRUG warfarin
  • DRUG edoxaban tosylate
  • DRUG enoxaparin/unfractionated heparin

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2012-08
Est. Completion 2014-03
Phase Phase 2

Sponsor

Daiichi Sankyo

236 total trials

What the Registry Record Tells You About NCT01662908

The ClinicalTrials.gov registry entry for NCT01662908 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 85 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Daiichi Sankyo, which has 236 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which warfarin is the first listed.

NCT01662908 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01662908 about?

NCT01662908 is a clinical study titled "A Randomized, Open-Label, Parallel-Group, Multi-Center Study for the Evaluation of Efficacy and Safety of Edoxaban Monotherapy Versus Low Molecular Weight (LMW) Heparin/Warfarin in Subjects With Symptomatic Deep-Vein Thrombosis". Assess the relative change in thrombus volume as determined by two assessments (Baseline and Day 14-21) with magnetic resonance venography (MRV) in subjects with deep-vein thrombosis (DVT) treated with either an edoxaban monotherapy regimen or a low molecular weight (LMW) heparin/warfarin regimen.

What is the current status of trial NCT01662908?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 85 participants. The study started on 2012-08. Estimated completion is 2014-03.

What interventions are being tested in trial NCT01662908?

The interventions under investigation include: warfarin (DRUG), edoxaban tosylate (DRUG), enoxaparin/unfractionated heparin (DRUG).

Who is sponsoring clinical trial NCT01662908?

This trial is sponsored by Daiichi Sankyo, which has 236 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.