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NCT01863550 · ClinicalTrials.gov registry record · Phase 3

Bortezomib or Carfilzomib With Lenalidomide and Dexamethasone in Treating Patients With Newly Diagnosed Multiple Myeloma

A Phase 3 study of Plasma Cell Myeloma, sponsored by ECOG-ACRIN Cancer Research Group.

Active
Registry status
Phase 3
Development phase
1,087
Enrollment target
20
Study locations

NCT01863550 is a Phase 3 study of Plasma Cell Myeloma that is active but no longer recruiting, run by ECOG-ACRIN Cancer Research Group. The registered enrollment target is 1,087 participants, above the 174-participant average among 32 other Plasma Cell Myeloma trials with a reported enrollment target (525% higher). The trial reports 20 study locations across 4 states.

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The verdict

NCT01863550, a Phase 3 study of Plasma Cell Myeloma, is active but no longer recruiting, sponsored by ECOG-ACRIN Cancer Research Group.

ACTIVE NOT RECRUITING
Registry status
Phase 3
Development phase
1,087 participants
Enrollment target
20
Study locations

Study Summary

This randomized phase III trial studies bortezomib, lenalidomide, and dexamethasone to see how well they work compared to carfilzomib, lenalidomide, and dexamethasone in treating patients with newly diagnosed multiple myeloma. Bortezomib and carfilzomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Lenalidomide may help the immune system kill abnormal blood cells or cancer cells. Drugs used in chemotherapy, such as dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. It is not yet known whether bortezomib, lenalidomide, and dexamethasone are more or less effective than carfilzomib, lenalidomide, and dexamethasone in treating patients with multiple myeloma

Conditions Studied

Interventions

  • OTHER Laboratory Biomarker Analysis
  • DRUG Dexamethasone
  • DRUG Lenalidomide
  • DRUG Carfilzomib
  • DRUG Bortezomib

Study Locations (20)

California

  • Kaiser Permanente-Deer Valley Medical Center - Antioch
  • PCR Oncology - Arroyo Grande
  • Sutter Auburn Faith Hospital - Auburn
  • Sutter Cancer Centers Radiation Oncology Services-Auburn - Auburn
  • Alta Bates Summit Medical Center-Herrick Campus - Berkeley
  • Providence Saint Joseph Medical Center/Disney Family Cancer Center - Burbank
  • Mills-Peninsula Medical Center - Burlingame
  • Sutter Cancer Centers Radiation Oncology Services-Cameron Park - Cameron Park
  • Eden Hospital Medical Center - Castro Valley
  • UC Irvine Health Cancer Center-Newport - Costa Mesa

Alaska

  • Anchorage Associates in Radiation Medicine - Anchorage
  • Alaska Breast Care and Surgery LLC - Anchorage
  • Alaska Oncology and Hematology LLC - Anchorage
  • Alaska Women's Cancer Care - Anchorage
  • Anchorage Oncology Centre - Anchorage
  • Katmai Oncology Group - Anchorage
  • Providence Alaska Medical Center - Anchorage

Arkansas

  • CHI Saint Vincent Cancer Center Hot Springs - Hot Springs
  • Veteran's Administration Medical Center - Little Rock

Arizona

  • Mayo Clinic in Arizona - Scottsdale

Trial Details

FieldValue
Enrollment Target 1,087 participants
Start Date 2013-12-06
Est. Completion 2034-02-05
Phase Phase 3

Sponsor

ECOG-ACRIN Cancer Research Group

75 total trials

What the Registry Record Tells You About NCT01863550

The ClinicalTrials.gov registry entry for NCT01863550 describes a study currently listed as active not recruiting, categorized as Phase 3. The registered enrollment target is 1,087 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 174-participant average among 32 other Plasma Cell Myeloma trials with a reported enrollment target (525% higher). The listed sponsor is ECOG-ACRIN Cancer Research Group, which has 75 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Plasma Cell Myeloma appearing as the primary indexed condition, and to 5 interventions - of which Laboratory Biomarker Analysis is the first listed.

NCT01863550 reports 20 study locations spanning 4 distinct geographic areas - top geographies include California, Alaska, Arkansas.

Frequently Asked Questions

What is clinical trial NCT01863550 about?

NCT01863550 is a clinical study titled "Bortezomib or Carfilzomib With Lenalidomide and Dexamethasone in Treating Patients With Newly Diagnosed Multiple Myeloma". This randomized phase III trial studies bortezomib, lenalidomide, and dexamethasone to see how well they work compared to carfilzomib, lenalidomide, and dexamethasone in treating patients with newly diagnosed multiple myeloma. Bortezomib and carfilzomib may stop the growth of cancer cells by blockin...

What is the current status of trial NCT01863550?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,087 participants. The study started on 2013-12-06. Estimated completion is 2034-02-05.

What conditions does trial NCT01863550 study?

This clinical trial studies the following conditions: Plasma Cell Myeloma.

What interventions are being tested in trial NCT01863550?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Dexamethasone (DRUG), Lenalidomide (DRUG), Carfilzomib (DRUG), Bortezomib (DRUG).

Who is sponsoring clinical trial NCT01863550?

This trial is sponsored by ECOG-ACRIN Cancer Research Group, which has 75 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01863550 being conducted?

This trial has 20 study locations across Alaska, Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.