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NCT03149003 · ClinicalTrials.gov registry record · Phase 3

A Study of DSP-7888 Dosing Emulsion in Combination With Bevacizumab in Patients With Recurrent or Progressive Glioblastoma Following Initial Therapy

A Phase 3 study, sponsored by Sumitomo Pharma America.

Completed
Registry status
Phase 3
Development phase
221
Enrollment target

NCT03149003 is a Phase 3 study that has completed, run by Sumitomo Pharma America. The registered enrollment target is 221 participants.

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The verdict

NCT03149003, a Phase 3 study, has completed, sponsored by Sumitomo Pharma America.

COMPLETED
Registry status
Phase 3
Development phase
221 participants
Enrollment target

Study Summary

This is an event driven, adaptive design, a randomized, active-controlled, multicenter, open-label, parallel groups, Phase 3 study of DSP-7888 Dosing Emulsion plus Bevacizumab versus Bevacizumab alone in patients with recurrent or progressive glioblastoma multiforme (GBM) following treatment with first line therapy consisting of surgery and radiation with or without chemotherapy.

Interventions

  • DRUG Bevacizumab
  • DRUG DSP-7888 Dosing Emulsion

Trial Details

FieldValue
Enrollment Target 221 participants
Start Date 2017-12-08
Est. Completion 2021-08-30
Phase Phase 3

Sponsor

Sumitomo Pharma America

168 total trials

What the Registry Record Tells You About NCT03149003

The ClinicalTrials.gov registry entry for NCT03149003 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 221 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sumitomo Pharma America, which has 168 total studies on file at ClinicalTrials.gov.

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

NCT03149003 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03149003 about?

NCT03149003 is a clinical study titled "A Study of DSP-7888 Dosing Emulsion in Combination With Bevacizumab in Patients With Recurrent or Progressive Glioblastoma Following Initial Therapy". This is an event driven, adaptive design, a randomized, active-controlled, multicenter, open-label, parallel groups, Phase 3 study of DSP-7888 Dosing Emulsion plus Bevacizumab versus Bevacizumab alone in patients with recurrent or progressive glioblastoma multiforme (GBM) following treatment with fi...

What is the current status of trial NCT03149003?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 221 participants. The study started on 2017-12-08. Estimated completion is 2021-08-30.

What interventions are being tested in trial NCT03149003?

The interventions under investigation include: Bevacizumab (DRUG), DSP-7888 Dosing Emulsion (DRUG).

Who is sponsoring clinical trial NCT03149003?

This trial is sponsored by Sumitomo Pharma America, which has 168 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.