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NCT07393282 · ClinicalTrials.gov registry record · Phase 3

A Study to Compare Linvoseltamab and Daratumumab Treatment in High-Risk Smoldering Multiple Myeloma (HR-SMM)

A Phase 3 study, sponsored by Regeneron Pharmaceuticals.

Recruiting
Registry status
Phase 3
Development phase
270
Enrollment target

NCT07393282: Recruiting Phase 3 study, sponsored by Regeneron Pharmaceuticals.

NCT07393282 is a Phase 3 study that is actively recruiting participants, run by Regeneron Pharmaceuticals. The registered enrollment target is 270 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07393282, a Phase 3 study, is actively recruiting participants, sponsored by Regeneron Pharmaceuticals.

RECRUITING
Registry status
Phase 3
Development phase
270 participants
Enrollment target

Study Summary

This study is researching an experimental drug called linvoseltamab (also called "study drug") compared to another drug called daratumumab, in participants with Smoldering Multiple Myeloma (SMM), who are at a High Risk (HR) of developing active multiple myeloma. The aim of this study is to find out whether linvoseltamab is better than daratumumab in delaying the development of MM. The study is looking at several other research questions, including: * What side effects may happen from taking the study drug * How much study drug is in the blood at different times * Whether the body makes antibodies against the study drug (which could make the drug less effective or could lead to side effects)

Interventions

  • DRUG Daratumumab
  • DRUG Linvoseltamab

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2026-05-21
Est. Completion 2033-07-27
Phase Phase 3
Regeneron Pharmaceuticals

280 total trials

What NCT07393282 shows while recruiting

NCT07393282 is an interventional study that assigns participants to a tested intervention. The registered 270 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (65% lower).

The record links to 0 conditions, and to 2 interventions - of which Daratumumab is the first listed.

NCT07393282 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07393282 about?

NCT07393282 is a clinical study titled "A Study to Compare Linvoseltamab and Daratumumab Treatment in High-Risk Smoldering Multiple Myeloma (HR-SMM)". This study is researching an experimental drug called linvoseltamab (also called "study drug") compared to another drug called daratumumab, in participants with Smoldering Multiple Myeloma (SMM), who are at a High Risk (HR) of developing active multiple myeloma. The aim of this study is to find out...

What is the current status of trial NCT07393282?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 270 participants. The study started on 2026-05-21. Estimated completion is 2033-07-27.

What interventions are being tested in trial NCT07393282?

The interventions under investigation include: Daratumumab (DRUG), Linvoseltamab (DRUG).

Who is sponsoring clinical trial NCT07393282?

This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07393282's enrollment target sits among peer trials

270 1217th of 2000 higher than 781 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT07393282, the US trial registry maintained by the National Library of Medicine. NCT07393282 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.