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A Study of STRO4 in Patients Amyotrophic Lateral Sclerosis (ALS)

A Study of STRO4 in Patients Amyotrophic Lateral Sclerosis (ALS)

Recruiting
18-75 years
All
Phase 2

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Overview

This study intends to evaluate the safety and efficacy of STR04 administered intravenously in participants with Amyotrophic Lateral Sclerosis.

Description

This study is a 69 week open label study of autologous bone-marrow-derived mesenchymal stem cells (STR04) in participants with ALS.

Participants will undergo a screening visit, followed by collection of peripheral blood and bone marrow for the manufacture of STR04. Once manufacturing is successfully completed, participants will have a Baseline visit followed by 4 doses of STR04, one dose every 12 weeks. Participants will have a final assessments 12 weeks after the 4th dose.

Eligibility

Inclusion
  • "Definite" or "Probable" ALS according to the Revised El Escorial criteria (Airlie House)
  • ALS severity grade 1 or 2 according to the Japan ALS severity classification.
  • ALSFRS-R scores of 2 or more for all items, with scores of 4 for all breathingrelated items (i.e., dyspnea, orthopnea, respiratory insufficiency).
  • Within 2 years of ALS onset.
  • %FVC of 80% or more.
  • Aged 18 to ≤75 years at the time of informed consent.
Exclusion
  • Current Viral Infection (e.g. HBV, HCV, HIV, HTLV-1, HPVB19, syphilis, COVID- 19).
  • Current low blood cell counts
  • History of cancer, congenital malformations, or chromosomal abnormalities
  • History of allergy to penicillin or streptomycin, or other serious allergies.
  • Current poor medical condition, due to endocrine disease, metabolic disease, immune disease, blood disease, psychiatric disorders, neurological diseases, cardiovascular diseases, respiratory diseases, gastrointestinal diseases, musculoskeletal or connective tissue diseases, renal or urogenital diseases.
  • History of intracranial lesions, or stenosis, dissection or severe atherosclerotic disease of a blood vessel in the head or neck.
  • Current uncontrolled hypertension.
  • Prior treatment with a cell or gene therapy.
  • Currently participating in any other clinical trial.
  • Women who are pregnant, breastfeeding, or plan to become pregnant during study participation
  • Men with plan for their partner to become pregnant during study participation.

Study details
    Amyotrophic Lateral Sclerosis

NCT06910384

New England Cell Therapeutics, Inc.

15 October 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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