Have you or a loved one undergone treatment for AL Amyloidosis without success?

Join the Future of AL Amyloidosis Treatment

Be part of a groundbreaking clinical trial exploring the potential of NXC-201, a cutting-edge CAR-T therapy designed for relapsed and refractory AL Amyloidosis.

About the NEXICART-2 Clinical Trial

ClinicalTrial.gov Identifier: NCT06097832

The NEXICART-2 clinical trial is dedicated to evaluating the safety and efficacy of our investigational CAR-T cell therapy (NXC-201) for patients with relapsed and refractory AL Amyloidosis. Participants can expect comprehensive care throughout the trial, including regular health assessments, monitoring, and support from our experienced medical team. By participating in the trial, you take an active role in allowing us to gather valuable research and data to advance the treatment of AL Amyloidosis with the goal of improving patient outcomes.

Understanding AL Amyloidosis

AL Amyloidosis is a rare and serious condition characterized by the buildup of amyloid proteins in organs and tissues, leading to organ dysfunction and severe health complications. These abnormal proteins, produced by dysfunctional plasma cells, can accumulate in the heart, kidneys, liver, spleen, nervous system, and digestive tract, impairing their function.

Patients with AL Amyloidosis often experience symptoms such as fatigue, swelling, weight loss, shortness of breath, and numbness or tingling in the extremities. The disease is particularly challenging because it often goes undiagnosed until it reaches an advanced stage, making early and effective treatment crucial.

Current treatments for AL Amyloidosis primarily involve chemotherapy and stem cell transplants, but many patients do not respond adequately to these therapies. This highlights the urgent need for new treatment options that can provide better outcomes for patients struggling with this debilitating disease.

Introducing NXC-201: A New Approach to Treating AL Amyloidosis

NXC-201 is an investigational CAR-T cell therapy designed to offer a new treatment option for patients with relapsed and refractory AL Amyloidosis. This innovative therapy harnesses the power of the patient’s own immune system to target and destroy the abnormal plasma cells responsible for producing amyloid proteins.

How It Works

CAR-T therapy involves collecting and modifying a patient’s T-cells, a type of immune cell, to express a chimeric antigen receptor (CAR) that specifically targets the disease-causing cells. Once these engineered CAR-T cells are infused back into the patient, they seek out and eliminate the amyloid-producing plasma cells, reducing the amyloid buildup and potentially restoring organ function.

Potential Benefits

NXC-201 represents a promising new direction in the treatment of AL Amyloidosis, offering potential to improve outcomes in patients who have exhausted other treatment options.

  • Targeted Action

    Unlike conventional treatments, NXC-201 directly targets and eliminates the source of amyloid production.

  • Personalized Therapy

    This approach uses the patient’s own immune cells, minimizing the risk of rejection and enhancing the specificity of the treatment.

  • Single Treatment​

    NXC-201 is designed to be administered as a single infusion, offering a potentially durable response without the need for ongoing treatment.

Eligibility Requirements for NEXICART-2 Clinical Trial

To participate in the NEXICART-2 clinical trial, patients must meet certain eligibility criteria. These criteria ensure that the trial is safe and appropriate for each participant and that the data collected will be scientifically valid.

  • Diagnosis

    Must have a confirmed diagnosis of AL Amyloidosis.

  • Treatment History

    Patients with relapsed or refractory AL Amyloidosis who have not responded adequately to previous treatments.

  • Age

    Participants must be 18 years or older.

  • Health Status

    Must have adequate organ function and performance status, as determined by the study investigators.

  • Consent

    Must be willing and able to provide informed consent.

This is not a full list of inclusion criteria and each case will be evaluated individually to be considered for the trial

Important Considerations

Other Medical Conditions: Patients with certain other medical conditions may not be eligible to participate. These conditions will be reviewed during the screening process.

Previous Therapies: Prior treatments and their outcomes will be considered to determine eligibility.

Commitment: Participants must be willing to comply with study procedures, including visits to the clinical trial site for monitoring and assessments.

If you or a loved one meets these criteria and is interested in participating in the NXC-201 clinical trial, please contact us to learn more about the enrollment process.

How to Enroll in the NEXICART-2 Clinical Trial

Enrolling in the NEXICART-2 clinical trial is a straightforward process designed to ensure that potential participants receive all the information they need and are fully supported throughout their journey.

For more information or to begin the enrollment process, please contact our clinical trial team at:

Patient Resources

At Immix Biopharma, we are committed to providing comprehensive support and resources to patients participating in the NEXICART-2 clinical trial. We understand that navigating a clinical trial can be challenging, and we are here to ensure that you have access to all the information and assistance you need.

Additional Resources

Treatment Options For Relapsed/refractory Systemic Light-Chain (AL) Amyloidosis: Current Perspectives