NCT05306457Active, not recruitingPhase 1
CNS10-NPC-GDNF Delivered to the Motor Cortex for ALS
Human Neural Progenitor Cells Secreting Glial Cell Line-Derived Neurotrophic Factor (CNS10-NPC-GDNF) Delivered to the Motor Cortex for the Treatment of Amyotrophic Lateral Sclerosis
Source: ClinicalTrials.gov · Last updated 19 Aug 2025
Brief summary (registry, in English)
The investigator is examining the safety of transplanting cells, that have been engineered to produce a growth factor, into the motor cortex (brain) of patients with Amyotrophic Lateral Sclerosis (ALS). The cells are called neural progenitor cells, which are a type of stem cell that can become several different types of cells in the nervous system. These cells have been derived to specifically become astrocytes, which is a type of neural cell. The growth factor is called glial cell line-derived neurotrophic factor, or GDNF. GDNF is a protein that promotes the survival of many types of neural cells. Therefore, the cells are called "CNS10-NPC-GDNF." The investigational treatment has been tested in people by delivering it to the spinal cord. However, it has only been delivered to the motor cortex of animals. In this study, we want to learn if CNS10-NPC-GDNF cells are safe to transplant into the motor cortex (brain) of people.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 16 (estimated)
- First submitted
- 21 Dec 2021
- Start date
- 8 May 2022
- Primary completion date
- Oct 2026
- Lead sponsor
- Cedars-Sinai Medical Center
- Diseases
- ALS (motor neurone disease)
- NCT number
- NCT05306457
What you commit to
- Study type: Interventional · Phase 1
- Planned participants: 16
- From 8 May 2022 to the primary completion date, Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- Inclusion:
- Confirmed diagnosis of ALS (Possible, Lab-supported Probable, Probable or Definite El Escorial Criteria)
- Duration of ALS symptoms ≤ 36 months
- Progressive weakness in upper extremities, with EMG supported evidence of denervation in both upper extremities
- Forced Vital Capacity ≥50% of predicted normal in supine
- Age: 18 years or older
- Able to provide Informed Consent
- Be geographically accessible to the study site and able to travel to study site for required visits
- Have caregiver to assist in the transportation and care required by participation in the study
- Not taking riluzole and/or edaravone or on a stable dose for ≥ 30 day
- For women of child bearing capacity, negative pregnancy test prior to surgery and willingness to use birth control for the duration of the trial.
- Medically able to undergo craniotomy as determined by the site PI and/or investigators
- Medically able to tolerate the immunosuppression regimen as determined by the site PI
- Exclusion:
- Using invasive ventilatory assistance
- Diagnosis of another active or unstable medical illness that may interfere with study participation at discretion of PI
- Presence of any of the following conditions:
- Current drug or alcohol abuse
- Any known immunodeficiency syndrome
- Unstable medical condition
- Unstable psychiatric illness including psychosis and untreated major depression within 90 days of screening
- Persons of child bearing capacity not willing to practice birth control
- Receiving any investigational device/biologic/drug in the past 30 days or any previous exposure to stem cell therapy
- Any condition in the upper extremities that precludes serial strength or coordination testing
- Any condition that the investigators feel may pose complications for the surgery
- Any condition or ALS disease phenotype that the site PI feels may interfere with participation in the study or in the interpretation of study endpoints
- Allergy to Beta-Lactam antibiotics
- Donor Specific Antibodies (DSA) ≥ 2500MFI or CPRA ≥ 20%
- Contraindications to MRI
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Cedars-Sinai Medical Center Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.