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Terminated Phase 1Phase 2 Interventional Results available

Oprozomib and Dexamethasone,in Combination With Lenalidomide or Oral Cyclophosphamide to Treat Newly Diagnosed Multiple Myeloma

ClinicalTrials.gov ID: NCT01881789

Public ClinicalTrials.gov record NCT01881789. 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 3, 2026, 8:57 AM EDT

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

Official title

Phase 1b/2, Multicenter, Open-label Study of Oprozomib and Dexamethasone, in Combination With Lenalidomide or Oral Cyclophosphamide in Patients With Newly Diagnosed Multiple Myeloma

Brief summary

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

The primary objectives of this study included the following: Phase 1b: * To establish the maximum tolerated dose (MTD) of oprozomib given in combination with lenalidomide and dexamethasone (ORd) or with cyclophosphamide and dexamethasone (OCyd) * To evaluate the safety and tolerability of oprozomib and dexamethasone administered in combination with lenalidomide or oral cyclophosphamide Phase 2: * To estimate the antitumor activity of each combination regimen, as measured by overall response rate (ORR) and complete response rate (CRR) * To evaluate the safety and tolerability of each combination regimens, as assessed by the type, incidence, severity and seriousness of adverse events, and abnormalities in selected laboratory analytes

Study identification

NCT ID
NCT01881789
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Amgen
Industry
Enrollment
22 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 27, 2013
Primary completion
Sep 22, 2019
Completion
Sep 22, 2019
Last update posted
Nov 13, 2022

2013 – 2019

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Clearview Cancer Institute Huntsville Alabama
Providence St. Joseph's Hospital Burbank California
David Geffen School of Medicine at UCLA Los Angeles California
Monterey Bay Oncology Corp DBA Pacific Cancer Care Salinas California
Colorado Blood Cancer Institute Denver Colorado
H. Lee Moffit Cancer Center & Research Institute Tampa Florida
University of Chicago Medical Center Chicago Illinois
Indiana University Health Melvin and Bren Simon Cancer Center Indianapolis Indiana
Center for Cancer & Blood Disorders Bethesda Maryland
The University of North Carolina at Chapel Hill Chapel Hill North Carolina
Cleveland Clinic Cleveland Ohio
University of Texas M.D. Anderson Cancer Center Houston Texas
Fred Hutchinson Cancer Research Center Seattle Washington
Froedtert Hospital and the Medical College of Wisconsin Milwaukee Wisconsin

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 NCT01881789, 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 Nov 13, 2022 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01881789 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →