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Completed Phase 2 Interventional

A Study of Filanesib (ARRY-520) and Carfilzomib in Patients With Advanced Multiple Myeloma

ClinicalTrials.gov ID: NCT01989325

Public ClinicalTrials.gov record NCT01989325. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 7:25 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 2 study during which patients with advanced multiple myeloma will receive either carfilzomib alone (single-agent) or carfilzomib in combination with investigational study drug filanesib (ARRY-520). Patients will be followed to determine the effectiveness of both single-agent carfilzomib and carfilzomib + filanesib in treating myeloma. Patients will be allowed to crossover from single-agent carfilzomib to carfilzomib + filanesib if disease progression occurs. Approximately 75 patients from the US will be enrolled in this study.

Study identification

NCT ID
NCT01989325
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
77 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2013
Primary completion
Jan 31, 2016
Completion
Apr 30, 2016
Last update posted
Sep 15, 2020

2013 – 2016

United States locations

U.S. sites
22
U.S. states
19
U.S. cities
22
Facility City State ZIP Site status
Genesis Cancer Center Hot Springs Arkansas 71913
UCLA Los Angeles California 90095
St. Joseph Heritage Healthcare Santa Rosa California 95403
Florida Cancer Specialists Fort Myers Florida 33905
Robert H. Lurie Comprehensive Cancer Center of Northwestern University Chicago Illinois 60611
Crescent City Research Consortium Marrero Louisiana 70072
Massachusetts General Hospital Boston Massachusetts 02114
Karmanos Cancer Institute Detroit Michigan 48201
Forrest General Cancer Center Hattiesburg Mississippi 39401
Nebraska Cancer Specialists Omaha Nebraska 68130
Memorial Sloan Kettering New York New York 10065
Levine Cancer Institute Charlotte North Carolina 28204
Oncology Hematology Care - Blue Ash Cincinnati Ohio 45242
Cleveland Clinic Cleveland Ohio 44195
Ohio State University Columbus Ohio 43210
Knight Cancer Institute at Oregon Health & Science University Portland Oregon 97239
Prairie Lakes Health Care System Watertown South Dakota 57201
Sarah Cannon Research Institute Nashville Tennessee 37203
Simmons Cancer Center - UT Southwestern Medical Center Dallas Texas 75390
Virginia Cancer Specialists Fairfax Virginia 22031
WVU - Mary Babb Randolph Cancer Center Morgantown West Virginia 26506
Medical College of Wisconsin Cancer Center Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01989325, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 15, 2020 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01989325 live on ClinicalTrials.gov.

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