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NCT02128230 · ClinicalTrials.gov registry record · Phase 2

UARK 2012-02 Trial For High-Risk Myeloma Evaluating Accelerating and Sustaining Complete Remission

A Phase 2 study, sponsored by University of Arkansas.

Terminated
Registry status
Phase 2
Development phase
20
Enrollment target

NCT02128230 is a Phase 2 study that was terminated before completion, run by University of Arkansas. The registered enrollment target is 20 participants.

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The verdict

NCT02128230, a Phase 2 study, was terminated before completion, sponsored by University of Arkansas.

TERMINATED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this study is to improve the clinical outcomes of research subjects with high-risk multiple myeloma in the context of the immediately preceding Total therapy 5 trial 2008-02 and Total therapy 3 trials 2003-33 and 2006-66.

Interventions

  • DEVICE myPRS
  • DRUG Induction 1 - MEL-10+CFZ-TD-PACE
  • DRUG First Transplant - MEL-80+CFZ-TD-PACE + PBSC (biologic)
  • DRUG Inter-Therapy - MEL-20+CFZ-TD-PACE (75%)
  • DRUG Second Transplant - MEL-80+CFZ-TD-PACE + PBSC (biologic)

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2014-06-10
Est. Completion 2019-02-19
Phase Phase 2

Sponsor

University of Arkansas

318 total trials

What the Registry Record Tells You About NCT02128230

The ClinicalTrials.gov registry entry for NCT02128230 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Arkansas, which has 318 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which myPRS is the first listed.

NCT02128230 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02128230 about?

NCT02128230 is a clinical study titled "UARK 2012-02 Trial For High-Risk Myeloma Evaluating Accelerating and Sustaining Complete Remission". The purpose of this study is to improve the clinical outcomes of research subjects with high-risk multiple myeloma in the context of the immediately preceding Total therapy 5 trial 2008-02 and Total therapy 3 trials 2003-33 and 2006-66.

What is the current status of trial NCT02128230?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2014-06-10. Estimated completion is 2019-02-19.

What interventions are being tested in trial NCT02128230?

The interventions under investigation include: myPRS (DEVICE), Induction 1 - MEL-10+CFZ-TD-PACE (DRUG), First Transplant - MEL-80+CFZ-TD-PACE + PBSC (biologic) (DRUG), Inter-Therapy - MEL-20+CFZ-TD-PACE (75%) (DRUG), Second Transplant - MEL-80+CFZ-TD-PACE + PBSC (biologic) (DRUG).

Who is sponsoring clinical trial NCT02128230?

This trial is sponsored by University of Arkansas, which has 318 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.