Anselamimab for AL Amyloidosis

MG
Overseen ByMani Gupta
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores a new treatment called anselamimab for individuals with AL amyloidosis, a condition characterized by abnormal protein buildup in organs. The study aims to assess anselamimab's ability to bind to these proteins, recruit immune cells, and reduce protein accumulation. Participants will receive the treatment through infusions over several weeks. Eligible participants should have confirmed AL amyloidosis without heart, kidney, or liver involvement from the disease. As an Early Phase 1 trial, this research focuses on understanding how anselamimab functions in people, offering participants the opportunity to be among the first to receive this new treatment.

Will I have to stop taking my current medications?

The trial requires that you stop taking doxycycline and any other investigational agents at least 30 days before screening.

Is there any evidence suggesting that anselamimab is likely to be safe for humans?

Previous studies have shown that patients tolerate anselamimab well. Research indicates that safety issues occurred at similar rates across different treatment groups, revealing no unexpected safety problems. Patients have used anselamimab for up to 110 weeks with consistent safety and tolerability. Although the treatment did not achieve all its goals in some studies, the safety record remained strong. This suggests that anselamimab is generally safe for humans, even as early trials continue.12345

Why do researchers think this study treatment might be promising for AL amyloidosis?

Unlike standard treatments for AL amyloidosis, which typically focus on chemotherapy and supportive care to manage symptoms, anselamimab offers a novel approach by directly targeting amyloid deposits. This treatment is unique because it uses the monoclonal antibody CAEL-101, which is designed to bind to and clear these harmful protein deposits from tissues. Researchers are excited about anselamimab because it has the potential to improve organ function and quality of life for patients by addressing the root cause of the disease rather than just alleviating symptoms.

What evidence suggests that anselamimab might be an effective treatment for AL amyloidosis?

Research has shown that anselamimab is designed to attach to amyloid fibrils, which are protein clumps that can accumulate in tissues and organs in conditions like AL amyloidosis. This attachment is believed to help clear these harmful protein deposits from the body. Some studies have found that anselamimab can help remove amyloid deposits, potentially improving organ function. However, a large study showed that anselamimab did not significantly improve survival for all patients. Despite this, certain patient groups experienced some benefits, indicating the need for more research to identify who might benefit most from this treatment. Participants in this trial will receive anselamimab to further evaluate its effectiveness and potential benefits.12456

Who Is on the Research Team?

ML

Michaela Liedtke, MD

Principal Investigator

Stanford University

Are You a Good Fit for This Trial?

This trial is for people diagnosed with AL amyloidosis who have measurable amyloid deposits in their tissues. Participants must meet specific health requirements set by the study team.

Inclusion Criteria

Hemoglobin ≥ 9 g/dL
AL amyloid deposit confirmed by biopsy and IHC or mass spectrometry
Amyloid deposits are measurable by imaging (ultrasound or cross-sectional)
See 12 more

Exclusion Criteria

I have not used any experimental drugs in the past 30 days.
I have a serious ongoing health problem with a major organ or body system.
I have or may have AL amyloidosis or other organ involvement.
See 13 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive anselamimab (CAEL-101) 1000 mg/m² by IV infusion weekly for 4 infusions, then every 2 weeks thereafter

48 weeks
Weekly for 4 weeks, then bi-weekly

Follow-up

Participants are monitored for safety and effectiveness after treatment

24 weeks
Assessments at Weeks 12, 24, 36, 48, and 72

What Are the Treatments Tested in This Trial?

Interventions

  • Anselamimab

Trial Overview

The study is testing a new drug called Anselamimab (also known as CAEL-101) to see how well it attaches to amyloid deposits, attracts immune cells, and helps reduce these harmful protein buildups.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: AnselamimabExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Stanford University

Lead Sponsor

Trials
2,527
Recruited
17,430,000+

Citations

Efficacy and Safety of Anselamimab in Immunoglobulin ...

Efficacy and Safety of Anselamimab in Immunoglobulin Light Chain Amyloidosis: Results From the Randomized CARES Trials ; Knowledge Generated.

Update on CARES Phase III clinical program of ...

Anselamimab is the first and only investigational fibril depleter to show clinical benefit in AL amyloidosis, and these results underscore its ...

3.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/42212672/

Efficacy and Safety of Anselamimab in Immunoglobulin ...

Anselamimab, a monoclonal antibody, selectively binds to amyloid fibrils, accelerating their clearance. Methods: Newly diagnosed patients with ...

A Study to Evaluate the Efficacy and Safety of CAEL-101 in ...

The primary purpose of this study is to determine whether CAEL-101, a monoclonal antibody that removes AL amyloid deposits from tissues and organs, improves ...

Anselamimab Misses Primary Endpoint in AL Amyloidosis ...

Findings showed the trial did not meet its primary endpoint in the overall study population; however, results from a pre-defined subgroup ...

Anselamimab Misses Primary Endpoint in Phase III CARES ...

Anselamimab did not meet the primary endpoint for advanced-stage AL amyloidosis, but a prespecified subgroup analysis revealed meaningful improvements in ...