Skip to main content
OpenTrials
Completed

NCT Number: NCT01335399

Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Treat Newly Diagnosed, Previously Untreated Multiple Myeloma

The purpose of the study is to determine whether the addition of Elotuzumab to Lenalidomide/low-dose Dexamethasone will increase the progression free survival (PFS)

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Local Institution - 3600, Garran, Australian Capital Territory, Australia

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com.

Inclusion criteria

  • Subjects who are newly diagnosed with symptomatic Multiple Myeloma (MM) and who:
  • have not received any prior systemic anti-myeloma therapy AND
  • have measurable disease AND
  • are not candidates for high-dose therapy plus stem-cell transplantation (SCT) because of age (≥ 65 years) or coexisting conditions. Refusal to undergo high dose therapy with SCT is NOT sufficient for entry onto CA204006 for a subject < 65 years old. There must be a comorbidity that prevents SCT for a subject < 65 years old

Exclusion criteria

  • Subjects with non-secretory or oligo-secretory or free light-chain only myeloma
  • Smoldering MM, defined as asymptomatic MM with absence of lytic bone lesions
  • Monoclonal Gammopathy of Undetermined Significance (MGUS)
  • Active plasma cell leukemia
  • Known Human Immunodeficiency Virus (HIV) infection or active hepatitis A, B, or C

Treatment and study plan

Lenalidomide

Drug

Capsules, Oral, 25 mg, once daily, on Days 1-21, Repeat every 28 days until subject meets criteria for discontinuation of study drug

Other names: Revlimid®

Dexamethasone

Drug

Tablets, Oral, 40 mg, weekly, on Days 1, 8, 15, 22, Repeat every 28 days until subject meets criteria for discontinuation of study drug

Other names: Decadron®, Dexamethasone Intensol®, Dexpak®, Taperpak®

Elotuzumab (BMS-901608; HuLuc63)

Biological

Solution, Intravenous (IV), 10 mg/kg, weekly, on Days 1, 8, 15, 22 (cycles 1&2); Days 1 and 15 (cycles 3-18), Repeat every 28 days until subject meets criteria for discontinuation of study drug

Primary outcomes

  1. Progression-Free Survival (PFS)

    Time frame: From randomization to date of first documented tumor progression or death due to any cause (up to 8 years)

    PFS is defined as the time from randomization to the date of the first documented tumor progression (as determined by the Independent Review Committee (IRC)) or death due to any cause.

    The IRC conducted a blinded, independent review of the tumor assessments based on the European Group for Blood and Bone Marrow Transplant (EBMT) criteria.

    Censoring rules applied:

    • Participants receiving subsequent systemic anti-myeloma therapy prior to documented progression were censored at the date of the last adequate tumor assessment prior to new therapy.
    • Participants who had an event (progression or death) > 10 weeks after their last tumor assessment were censored at their last adequate tumor assessment prior to the event.
    • Participants without progression or death (and not receiving subsequent therapy prior to progression) were censored at their last adequate tumor assessment.
    • Participants without any post-baseline tumor assessments were censored on the date of randomization

Secondary outcomes

  1. Objective Response Rate (ORR)

    Time frame: From randomization to primary completion date (approximately 8 years)

    ORR is defined as the percentage of participants with objective response among all randomized subjects. Participants with an objective response are those participants experiencing a partial response (PR) or better, based on Independent Review Committee (IRC) assessment, as per EBMT criteria.

  2. Overall Survival (OS)

    Time frame: From randomization to the date of death (up to 8 years)

    Survival is defined as the time from randomization to the date of death. A participant who did not die had his or her survival duration censored at the date of last contact ('last known date alive").

  3. Mean Change From Baseline of Pain Severity Score and Pain Interference Score

    Time frame: From Baseline to End of Treatment (approximately 8 years)

    Pain severity (sensory dimension) and pain interference (reactive dimension, assessing the degree to which pain interferes with function) are measured using the Brief Pain Inventory- Short Form (BPI-SF).

    BPI-SF numeric rating scale goes from 0 (No pain) to 10 (Pain as bad as you can imagine).

  4. Progression Free Survival (PFS) Rate at Specific Time-points

    Time frame: From randomization to the specified time-point (up to 5 years)

    PFS rate is defined as the percentage of participants experiencing PFS at the defined time-points.

Sponsors and collaborators

Lead sponsor

Bristol-Myers Squibb

Industry

Collaborators

  • AbbVie

Registry information

Official study title

A Phase 3, Randomized, Open Label Trial of Lenalidomide/Dexamethasone With or Without Elotuzumab in Subjects With Previously Untreated Multiple Myeloma

Acronym: ELOQUENT - 1

Important dates

Study start
2011
Primary completion
2019
Study completion
2021
First posted
Apr 14, 2011
Registry last updated
Sep 30, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.