120 Participants NeededMy employer runs this trial

Fianlimab + Cemiplimab for Head and Neck Cancer

Recruiting at 34 trial locations
CT
Overseen ByClinical Trials Administrator
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new drug combination for head and neck cancer that has returned or spread. Researchers aim to determine if fianlimab (an experimental treatment) combined with cemiplimab (a type of immunotherapy) is more effective than cemiplimab with a placebo. They are also examining side effects and the body's response to these drugs. Individuals with head and neck cancer that cannot be cured with local treatments and who have not received prior treatment for their recurrent or metastatic cancer might be suitable candidates. As a Phase 2 trial, the research focuses on assessing the treatment's effectiveness in an initial, smaller group of participants.

Do I need to stop my current medications for the trial?

The trial does not specify if you need to stop taking your current medications. However, if you are on corticosteroid therapy at a dose higher than 10 mg per day, you must stop it at least 14 days before starting the study drugs.

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

Research has shown that the combination of fianlimab and cemiplimab appears safe for patients with head and neck cancers. In earlier studies, most participants tolerated this combination well, and its safety was deemed acceptable. However, some experienced significant side effects. Specifically, 43.9% had severe treatment-related side effects, and 32.7% faced serious immune system-related issues.

Cemiplimab alone has proven safe and well-tolerated, even in older patients with other health conditions. While the combination looks promising, it carries some risks, as with any treatment. Participants should consider these factors and discuss them with their doctor.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about Fianlimab and Cemiplimab for head and neck cancer because these treatments work by targeting specific immune checkpoints, potentially boosting the body's own immune response to fight cancer. Unlike the standard chemotherapy or radiation treatments, which attack both cancerous and healthy cells, Fianlimab and Cemiplimab aim to enhance the immune system's ability to identify and destroy cancer cells more precisely. This targeted approach may result in fewer side effects and improved effectiveness, especially in individuals with HPV-positive or HPV-negative head and neck squamous cell carcinoma (HNSCC).

What evidence suggests that this trial's treatments could be effective for head and neck cancer?

Studies have shown that combining fianlimab with cemiplimab holds promise for treating head and neck cancer. Earlier research demonstrated that patients with squamous cell carcinoma, a type of head and neck cancer, responded well to this combination, experiencing long-lasting effects. Specifically, one study found that 57% of patients experienced tumor shrinkage or disappearance, indicating positive results for more than half of the participants. In this trial, participants in Cohort 1 will receive either the combination of fianlimab and cemiplimab or cemiplimab with a placebo. These findings suggest that adding fianlimab to cemiplimab might improve outcomes compared to cemiplimab alone. The combination has also proven safe for patients, which is crucial for treatment.23467

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 with head and neck squamous cell carcinoma that has come back or spread, who haven't had treatment for this advanced cancer. Participants must have a measurable tumor, good physical health (ECOG 0-1), certain lab results showing healthy organs, and specific test results on their tumors.

Inclusion Criteria

I have at least one tumor that can be measured on scans.
I am fully active or have only minor physical limitations.
I have head and neck cancer that cannot be cured with local treatments.
See 4 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive Fianlimab plus Cemiplimab or Cemiplimab plus placebo

Approximately 58 months

Follow-up

Participants are monitored for safety and effectiveness after treatment

Up to 90 days

What Are the Treatments Tested in This Trial?

Interventions

  • Cemiplimab
  • Fianlimab

Trial Overview

The study compares two treatments: one group gets both fianlimab (an experimental drug) and cemiplimab; the other group gets cemiplimab plus a placebo. The goal is to see if adding fianlimab helps more than cemiplimab alone in treating these cancers.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Cohort 2Experimental Treatment3 Interventions
Group II: Cohort 1Experimental Treatment3 Interventions

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

A phase 1 study of fianlimab (anti–LAG-3) in combination ...

Conclusions: Fianlimab + cemiplimab in pts with HNSCC showed signs of clinical activity with durable responses among pts with anti–PD-1/PD-L1- ...

Safety and Activity Profile of Fianlimab (Anti–LAG-3) in ...

Cemiplimab monotherapy and fianlimab + cemiplimab combination demonstrated signs of clinical activity and an acceptable safety profile in anti– ...

Fianlimab, a human lymphocyte activation gene‐3 ... - PMC

Here, we present clinical activity and safety data from additional expansion cohorts of fianlimab plus cemiplimab in patients with advanced non– ...

NCT06769698 | A Study to See if Giving Fianlimab and ...

The study is focused on participants with head and neck cancers who have not been previously treated for head and neck cancer that has come back or spread to ...

"A phase 1 study of fianlimab (anti-LAG-3) in combination ...

We present safety and clinical activity data from a Phase 1 study in patients (pts) with head and neck squamous cell carcinomas (HNSCC) treated ...

Safety and Activity Profile of Fianlimab (Anti–LAG-3) in ...

Cemiplimab monotherapy and fianlimab + cemiplimab combination demonstrated signs of clinical activity and an acceptable safety profile in anti– ...

Evaluating fianlimab and cemiplimab in PD-L1+ recurrent ...

The combination of an antiPD1 and an anti lag 3 is superior to an antiPD1 alone. We have promising data with the combination.