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NCT02294357 · ClinicalTrials.gov registry record · Phase 2

Weekly 70 mg/m2 Carfilzomib for Multiple Myeloma Patients Refractory to 27 mg/m2 Carfilzomib

A Phase 2 study, sponsored by Oncotherapeutics.

Terminated
Registry status
Phase 2
Development phase
45
Enrollment target

NCT02294357 is a Phase 2 study that was terminated before completion, run by Oncotherapeutics. The registered enrollment target is 45 participants.

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The verdict

NCT02294357, a Phase 2 study, was terminated before completion, sponsored by Oncotherapeutics.

TERMINATED
Registry status
Phase 2
Development phase
45 participants
Enrollment target

Study Summary

The purpose of this Phase II study is to evaluate the safety and effectiveness (good and bad effects) of carfilzomib given as a 30-minute infusion and at a dose of 70 mg/m2 to treat patients with multiple myeloma (MM), who are currently showing progressive disease (worsening) and had progressed (did not respond to treatment) within 8 weeks of receiving treatment with twice weekly 27mg/m2 of carfilzomib. Carfilzomib is approved by the U.S. Food and Drug Administration (FDA) to be used only in certain U.S. patients with relapsed and refractory multiple myeloma that have tried and failed other therapies. Carfilzomib is considered an investigational drug for this study because the dose and regimen included in this study are different from the FDA approved carfilzomib regimen. Carfilzomib is a type of drug called a proteasome inhibitor. Carfilzomib is thought to work by preventing breakdown of abnormal proteins in cells, causing the cells to die. Cancer cells are more sensitive to these effects than normal cells. Carfilzomib has been previously given to more than 1800 people in clinical trials.

Interventions

  • DRUG Dexamethasone
  • DRUG Lenalidomide
  • DRUG Prednisone
  • DRUG Methylprednisolone
  • DRUG Carfilzomib

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2014-12
Est. Completion 2020-09-22
Phase Phase 2

Sponsor

Oncotherapeutics

17 total trials

What the Registry Record Tells You About NCT02294357

The ClinicalTrials.gov registry entry for NCT02294357 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Oncotherapeutics, which has 17 total studies on file at ClinicalTrials.gov.

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

NCT02294357 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02294357 about?

NCT02294357 is a clinical study titled "Weekly 70 mg/m2 Carfilzomib for Multiple Myeloma Patients Refractory to 27 mg/m2 Carfilzomib". The purpose of this Phase II study is to evaluate the safety and effectiveness (good and bad effects) of carfilzomib given as a 30-minute infusion and at a dose of 70 mg/m2 to treat patients with multiple myeloma (MM), who are currently showing progressive disease (worsening) and had progressed (did...

What is the current status of trial NCT02294357?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 45 participants. The study started on 2014-12. Estimated completion is 2020-09-22.

What interventions are being tested in trial NCT02294357?

The interventions under investigation include: Dexamethasone (DRUG), Lenalidomide (DRUG), Prednisone (DRUG), Methylprednisolone (DRUG), Carfilzomib (DRUG).

Who is sponsoring clinical trial NCT02294357?

This trial is sponsored by Oncotherapeutics, which has 17 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.