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Completed Phase 3 Interventional Results available

A Study Comparing Once-weekly vs Twice-weekly Carfilzomib in Combination With Lenalidomide and Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT03859427

Public ClinicalTrials.gov record NCT03859427. 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 Oct 9, 2026, 8:31 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

A Randomized, Open-label, Phase 3 Study Comparing Once-weekly vs Twice-weekly Carfilzomib in Combination With Lenalidomide and Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma (A.R.R.O.W.2)

Brief summary

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

Compare efficacy of 56 mg/m2 carfilzomib administered once-weekly in combination with lenalidomide and dexamethasone (KRd 56 mg/m2) to 27 mg/m2 carfilzomib administered twice-weekly in combination with lenalidomide and dexamethasone (KRd 27 mg/m2) in subjects with relapsed or refractory multiple myeloma (RRMM) with 1 to 3 prior lines of therapy.

Study identification

NCT ID
NCT03859427
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
454 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
May 8, 2019 (Actual)
Primary completion
Mar 31, 2023 (Actual)
Completion
Mar 31, 2023 (Actual)
Last update posted
Aug 13, 2024

2019 – 2023

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
Robert A Moss Oncology Fountain Valley California 92708 —
Rocky Mountain Cancer Centers Denver Midtown Denver Colorado 80218 —
Hartford HealthCare Cancer Institute at The Hospital of Central Connecticut Plainville Connecticut 06062 —
Baptist MD Anderson Cancer Center Jacksonville Florida 32207 —
Advocate Lutheran General Hospital Park Ridge Illinois 60068 —
New York Oncology Hematology, PC Albany New York 12208 —
Oncology Hematology Care Inc Cincinnati Ohio 45242 —
Texas Oncology-Denton Denton Texas 76201 —
US Oncology Research Investigational Products Center Fort Worth Texas 76177 —
Oncology Consultants PA Houston Texas 77030 —
Texas Oncology San Antonio Texas 78229 —
United States Oncology Regulatory Affairs Corporate Office The Woodlands Texas 77380 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 96 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03859427, 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 Aug 13, 2024 · Synced Oct 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03859427 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →