Clinical Trials Directory

Trials / Completed

CompletedNCT02987413

Escalated Application of Mesenchymal Stem Cells in Amyotrophic Lateral Sclerosis Patients

Safety and Efficacy of Mesenchymal Stem Cells Escalated Application in Amyotrophic Lateral Sclerosis Patients: Study Design of a Phase I Trial

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
3 (actual)
Sponsor
Hospital e Maternidade Dr. Christóvão da Gama · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that selectively affects motor neurons in the brain and spinal cord, leading to bulbar, respiratory, and limb weakness. There is no effective treatment, and the disease usually progresses to death within 2 to 4 years. The therapeutic plasticity of mesenchymal stem cells (MSCs) may be an attractive therapy to this complex disease, turning MSCs strong candidates for cellular therapy in ALS. Design-A phase 1 open-safety clinical trial. 4 patients will be selected according to a restricted inclusion and exclusion criteria and after 2 escalated infusions of MSCs, there will be a follow up period of one year Methods - Primary endpoint: safety of mesenchymal autologous stem cells infusions escalated in two intrathecal administrations in patients with ALS defined as severe adverse events (SAe). Secondary endpoints: clinical response, laboratorial and magnetic resonance imaging of patients submitted to cellular escalating doses applied in the study. Quality of life, according to El Escorial criteria, ALSFR scale and functional scales. Conclusion: This study is a primary step before a large randomized double-blind clinical trial for ALS. It is expected to confirm the safety of escalated MSCs therapy in ALS patients, initial data of efficacy in addition to improved quality of life.

Conditions

Interventions

TypeNameDescription
BIOLOGICALAutologous Mesenchymal stem cells (MSCs)2 intrathecal autologous MSCs infusions (1x10\^8 cells) will be performed, escalated from 30 days apart

Timeline

Start date
2015-04-28
Primary completion
2016-03-01
Completion
2017-04-05
First posted
2016-12-09
Last updated
2017-08-07

Locations

2 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02987413. Inclusion in this directory is not an endorsement.