270 Participants NeededMy employer runs this trial

Linvoseltamab vs Daratumumab for Multiple Myeloma

(LINKER-SMM2 Trial)

Recruiting at 14 trial locations
CT
Overseen ByClinical Trials Administrator
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new drug, linvoseltamab, to determine if it can delay the onset of multiple myeloma (a type of blood cancer) more effectively than the existing drug, daratumumab. Researchers aim to assess whether linvoseltamab benefits individuals with Smoldering Multiple Myeloma (SMM) who face a high risk of developing active multiple myeloma. The trial will also evaluate any side effects, how the body processes the drug, and whether the body develops antibodies against it. Individuals with high-risk SMM who have not undergone certain previous treatments might be suitable candidates for this study. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to potentially groundbreaking treatment advancements.

Do I have to stop taking my current medications for the trial?

The trial does not specify if you must stop taking your current medications, but it does exclude those who have had prior treatments for plasma cell disorders or are on treatments that might interfere with the study. It's best to discuss your specific medications with the trial team.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Previous studies have shown that linvoseltamab is safe for patients with multiple myeloma. Research indicates that most people tolerate the drug well, though some participants experienced side effects that could be managed or treated with other medications. The FDA has granted accelerated approval to linvoseltamab for certain types of multiple myeloma, reflecting confidence in its safety for those conditions.

Daratumumab, already approved for treating multiple myeloma, has undergone thorough testing to ensure its safety for that condition. Participants in studies often report mild to moderate side effects, which are usually manageable.

Both treatments have been tested in people before, and their safety records suggest they are generally well-tolerated. However, all medications can have side effects, and individual experiences may vary. Always discuss any concerns with a healthcare provider.12345

Why do researchers think this study treatment might be promising for multiple myeloma?

Linvoseltamab is unique because it represents a novel approach to treating multiple myeloma. While most treatments for multiple myeloma, like Daratumumab, target CD38 proteins on myeloma cells, Linvoseltamab targets a different protein called BCMA (B-cell maturation antigen). This new mechanism of action offers potential for improved efficacy, particularly in patients who have become resistant to existing treatments. Researchers are excited about Linvoseltamab due to its ability to engage the immune system in a new way, potentially leading to better outcomes for patients with this challenging cancer.

What evidence suggests that this trial's treatments could be effective for Smoldering Multiple Myeloma?

This trial will compare Linvoseltamab and Daratumumab for treating multiple myeloma. Research has shown that Linvoseltamab, which participants in this trial may receive, yields promising results for patients with multiple myeloma, a type of blood cancer. In some studies, Linvoseltamab significantly reduced cancer cells and maintained low levels for extended periods. Many patients experienced a measurable reduction in cancer and lived longer without disease progression. Although less information exists on its use for smoldering multiple myeloma (an early stage of the disease), its success in treating advanced cases suggests potential benefits.

Conversely, Daratumumab, the comparator treatment in this trial, is already an approved treatment for multiple myeloma and has effectively slowed the disease. It targets a specific protein on cancer cells, aiding the immune system in destroying them. While Linvoseltamab remains under study, Daratumumab has a proven track record in treating multiple myeloma.23678

Who Is on the Research Team?

CT

Clinical Trial Management

Principal Investigator

Regeneron Pharmaceuticals

Are You a Good Fit for This Trial?

This trial is for adults diagnosed with high-risk smoldering multiple myeloma (HR-SMM) who are otherwise in good physical condition and meet specific risk criteria. Participants must not have active multiple myeloma or other serious health issues.

Inclusion Criteria

I have been diagnosed with smoldering multiple myeloma.
I have high-risk smoldering multiple myeloma as defined by risk models.
I am fully active or restricted in physically strenuous activity only.

Exclusion Criteria

I have symptoms or signs that show my myeloma is active.
I have been diagnosed with a specific plasma cell or lymphoplasmacytic disorder.
I have a history of a brain or nerve disorder.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either linvoseltamab or daratumumab to assess efficacy in delaying the development of multiple myeloma

Up to 5 years

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Daratumumab
  • Linvoseltamab

Trial Overview

The study compares an experimental drug, linvoseltamab, to daratumumab in people with HR-SMM. The goal is to see which drug better delays the progression to active multiple myeloma. Participants are randomly assigned to one of the two treatments.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: LinvoseltamabExperimental Treatment1 Intervention
Group II: DaratumumabActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Regeneron Pharmaceuticals

Lead Sponsor

Trials
690
Recruited
948,000+
Founded
1988
Headquarters
Tarrytown, USA
Known For
Precision medicine
Top Products
Dupixent, EYLEA, Libtayo, Praluent
Leonard Schleifer profile image

Leonard Schleifer

Regeneron Pharmaceuticals

Chief Executive Officer since 1988

MD and PhD in Medicine

George Yancopoulos profile image

George Yancopoulos

Regeneron Pharmaceuticals

Chief Medical Officer since 1997

MD from Harvard Medical School

Citations

Effectiveness of linvoseltamab versus real-world standard ...

most patients eventually relapse, become refractory, or both, with a median overall survival (OS) of approximately 5.5 years from diagnosis

Linvoseltamab Adds Highly Effective Option in Later-Line ...

Data from LINKER-MM1 revealed that patients who received the BCMA-directed CD3 T-cell engager (n = 80) experienced an objective response rate ( ...

Linvoseltamab for Treatment of Relapsed/Refractory ...

Linvoseltamab 200 mg induced deep and durable responses, with a median DOR of 29.4 months, in patients with RRMM with an acceptable safety profile.

Linvoseltamab in Combination with Carfilzomib or ...

With a median follow-up of 15 months, efficacy results across all dose levels showed a 90% objective response rate (ORR; 19 of 21 patients), with 76% (16 of 21 ...

Indirect Comparison of Linvoseltamab Versus Teclistamab ...

linvoseltamab showed significantly longer progression-free survival (PFS, P = .004), overall survival (OS, P = .039), and time to next treatment

Linvoseltamab Yields Favorable Safety Profile and ...

Linvoseltamab-gcpt showed a 100% overall response rate in high-risk smoldering multiple myeloma patients, with significant MRD negativity rates.

Linvoseltamab in Patients With Relapsed/Refractory ...

Linvoseltamab, a BCMA × CD3 bispecific antibody, demonstrated durable efficacy and generally manageable safety in patients with relapsed/refractory multiple ...

INTERVIEW: Linvoseltamab Shows Durable Efficacy, ...

Linvoseltamab showed a 71% overall survival rate and 52% complete response rate in relapsed, refractory multiple myeloma patients. High-risk ...