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NCT03411031 · ClinicalTrials.gov registry record · Phase 2

Elotuzumab Plus Lenalidomide (Elo/Rev) for Serologic Relapse/Progression While on Lenalidomide

A Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

Terminated
Registry status
Phase 2
Development phase
18
Enrollment target

NCT03411031: Clinical Trial Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

NCT03411031 is a Phase 2 study that was terminated before completion, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 18 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03411031, a Phase 2 study, was terminated before completion, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

TERMINATED
Registry status
Phase 2
Development phase
18 participants
Enrollment target

Study Summary

The purpose of this study is determine Time-to-Progression with elotuzumab plus lenalidomide when elotuzumab is added to multiple myeloma participants with serologic relapse/progression while receiving lenalidomide maintenance for each study arm.

Primary Outcome

Progression free survival (PFS) is defined as the time of randomization to date of death from any cause, date of relapse/progression, or the last follow-up date, whichever comes first. The Kaplan-Meier method will be used to estimate PFS for each Study Arm. The method of Brookmeyer and Crowley will be used to construct 95% confidence interval.

Interventions

  • DRUG Dexamethasone
  • DRUG Lenalidomide
  • DRUG Elotuzumab

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2018-10-04
Est. Completion 2021-11-04
Phase Phase 2

Why NCT03411031 stopped before completion

NCT03411031 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower).

The record links to 0 conditions, and to 3 interventions - of which Dexamethasone is the first listed.

NCT03411031 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03411031 about?

NCT03411031 is a clinical study titled "Elotuzumab Plus Lenalidomide (Elo/Rev) for Serologic Relapse/Progression While on Lenalidomide". The purpose of this study is determine Time-to-Progression with elotuzumab plus lenalidomide when elotuzumab is added to multiple myeloma participants with serologic relapse/progression while receiving lenalidomide maintenance for each study arm.

What is the current status of trial NCT03411031?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 18 participants. The study started on 2018-10-04. Estimated completion is 2021-11-04.

What interventions are being tested in trial NCT03411031?

The interventions under investigation include: Dexamethasone (DRUG), Lenalidomide (DRUG), Elotuzumab (DRUG).

Who is sponsoring clinical trial NCT03411031?

This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03411031's enrollment target sits among peer trials

18 1898th of 2000 higher than 98 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03411031, the US trial registry maintained by the National Library of Medicine. NCT03411031 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.