Safety/Efficacy Study for the Treatment of Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis Clinical Trial

— ALS  

Official title:

Phase I, Single Center, Prospective, Non-randomized, Open Label, Safety/Efficacy Study of the Infusion of Autologous Bone Marrow-derived Stem Cells, in Patients With Amyotrophic Lateral Sclerosis

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT01082653
• Other study ID #: 2008-ALS-I
• Status: Suspended
• Phase: Phase 1
• First received: March 1, 2010
• Last updated: May 7, 2014
• Start date: March 2010
• Est. completion date: May 2014

Study information

• Verified date: September 2013
• Source: TCA Cellular Therapy
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

A Phase I, single center, prospective, non-randomized, open label, safety/efficacy study of the infusion of autologous bone marrow-derived stem cells, in 6 patients with Amyotrophic Lateral Sclerosis according to established criteria (1), (2) with a moderate to severe diagnosis of ALS according to the World Federation of Neurology El Escorial criteria.

The primary purpose of this study is to evaluate safety of the infusion procedure, as assessed by absence of complications at the site of infusion or the appearance of new neurologic deficit not attributed to the natural progression of the disease.

Secondary outcomes will include a)neurological evidence of trends toward a slowing down of the decline of the forced vital capacity (FVC) (3) and of the functional rating scale (ALS-FRS) scores, as assessed at 3-month intervals, b)evidence of a decline of the maximum voluntary isometric contraction-arm (MVIC-arm) and MVIC-grip Z (4) scores and c)patient evaluation that the treatment was effective and consider the possibility of a new cell product stem cell infusion.

Subjects who fulfill inclusion/exclusion criteria and sign informed consent will undergo an aspiration of bone marrow from the iliac crest for preparation of the cellular product.

The day of infusion, the investigational product will be injected into the patient's intrathecal space.

After cell infusion patients will be followed at WK 2, MN 1, MN 2, MN 6 and a long-term followup at MN 12 in the clinic and/or office. Electromyographic (EMG) studies, Forced vital capacity (FVC), functional rating scale (FRS) and maximum voluntary isometric contraction-arm (MVIC-arm) and MVIC-grip Z scores will have been used to assess the status of the disease before (historical record acceptable if done within three months of Screening Visit) and during the 12-month study period after cell infusion.

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 6
• Est. completion date: May 2014
• Est. primary completion date: May 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Adult male and female subjects > 18 years of age.

2. Good understanding of the protocol and willingness to consent.

3. Moderate to severe Diagnosis of ALS according to the World Federation of Neurology El Escorial criteria.

4. Vital capacity at least 50% predicted value for gender, height and age.

5. More than 6 and less than 36 months of evolution of the disease.

6. Hematocrit greater than 30 % prior to bone marrow aspiration.

7. Platelet count greater than 100 Thousand/uL at screening.

8. INR less than or equal to 1.5.

Exclusion Criteria:

1. Any concurrent illness, which affects the bone marrow.

2. Any concomitant medication that affects the bone marrow.

3. Previous stem cell therapy.

4. Any lymphoproliferative disease.

5. Riluzole with 4 weeks of study entry and at any time during the study.

6. Hemophiliacs or subjects with bleeding disorders.

7. Known hypersensitivity to fetal bovine serum

8. HIV infection.

9. Serum creatinine > 3.0 in subjects not on hemodialysis.

10. Skin infection at the infusion site or systemic infection

11. Current smoker.

12. Active drug or alcohol addiction

13. Pregnant, planning to become pregnant or not on accepted birth control method if subject is of child bearing potential.

14. Subjects that are breast feeding.

15. Any condition that the Principal Investigator considers would render the subject unfit for the study.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Amyotrophic Lateral Sclerosis
• Motor Neuron Disease
• Sclerosis

Intervention

Biological:
• autologous bone marrow-derived stem cells
All patients will receive a unique one-time intrathecal infusion of the cell product suspended in infusion medium.

Locations

Country	Name	City	State
United States	TCA Cellular Therapy	Covington	Louisiana

Sponsors (1)

Lead Sponsor	Collaborator
TCA Cellular Therapy

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety	Safety of the infusion procedure, as assessed by absence of complications at the site of infusion or the appearance of new neurologic deficit not attributed to the natural progression of the disease.	one year	Yes
Secondary	Efficacy	Neurological evidence of trends toward a slowing down of the decline of the forced vital capacity and of the functional rating scale scores, as assessed at 3 month intervals.; Evidence of a decline of the maximum voluntary isometric contraction-arm (MVIC-arm) and MVIC-grip Z scores.; Patient evaluation that the treatment was effective.	one year	No