A Biomarker Study to Evaluate MN-166 (Ibudilast) in Subjects With Amyotrophic Literal Sclerosis (ALS)

Amyotrophic Lateral Sclerosis Clinical Trial

Official title:

A Multi-Center, Open-Label Biomarker Study to Evaluate MN-166 (Ibudilast) in Subjects With Amyotrophic Literal Sclerosis (ALS)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02714036
• Other study ID #: MN-166-ALS-1202
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: May 6, 2016
• Est. completion date: June 30, 2020

Study information

• Verified date: July 2020
• Source: MediciNova
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multi-center, open-label study of MN-166 (ibudilast) in subjects with ALS. To be eligible subjects must meet the El Escorial criteria of possible, laboratory-supported probable, probable, or definite criteria for a diagnosis of ALS. Safety, tolerability, blood, neuro-imaging biomarkers, and clinical outcomes will be collected on all subjects. Subjects will receive study drug for 36 weeks.

The study will consist of a Screening Phase (up to 6 weeks), an Open-Label Treatment Phase (36 weeks) and a Off-Treatment Follow-up Phase (4 Weeks).

Number of Subjects (Planned):

Approximately 45 subjects are planned to be screened with the goal of enrolling 35 subjects.

Description:

This is a multi-center, open-label study of MN-166 (ibudilast) in subjects with ALS. To be eligible subjects must meet the El Escorial criteria of possible, laboratory-supported probable, probable, or definite criteria for a diagnosis of ALS. Safety, tolerability, blood, neuro-imaging biomarkers, and clinical outcomes will be collected on all subjects. Subjects will receive study drug for 36 weeks.

The study will consist of a Screening Phase (up to 6 weeks), an Open-Label Treatment Phase (36 weeks) and a Off-Treatment Follow-up Phase (4 Weeks).

During the Screening Phase, eligible ALS subjects will sign an informed consent form and the following screening assessments will be performed: review of inclusion/exclusion criteria: El Escorial ALS Diagnostic criteria, medical history and demographics, ALS diagnosis history, physical and neurological examination, U. Penn upper motor Neuron Burden (UMNB), pulmonary function tests, vital signs including height and weight, blood for safety labs including TSPO affinity test, ECG and review and documentation of concomitant medications and therapies.

Screening Phase (up to 6 weeks) The Treatment Phase will consist of a Baseline visit and 3 subsequent clinic visits at Weeks 4, 12, 24, and 36. Telephone follow-ups will occur at Weeks 1, 2, 8, 16, 20, 28, and 32.

Open-Label Treatment Phase (36 weeks) At the Baseline visit, subjects will return to the clinic and the following assessments will be performed/administered: review of inclusion and exclusion criteria for continued eligibility, vital signs, blood for safety labs and biomarkers, ECG, ALSFRS-R questionnaire, slow vital capacity (SVC), baseline strength as measured by hand held dynamometry (HHD), and Columbia Suicide Severity Rating Scale (C-SSRS). At this visit, study drug will be dispensed, and adverse events, concomitant medications and therapies will be assessed and documented. At subsequent visits during the Treatment Phase, similar assessments will be performed.

In addition, a [11C]PBR28-PET scan will be performed once between the Screening and Baseline visit, and once between the Week 20 and Week 28 phone calls. The ALSFRS-R, SVC and U Penn Upper Motor Neuron Burden will be repeated on the same day as the PET scans.

The follow-up visit will consist of a telephone call to document adverse events and concomitant therapies

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. completion date: June 30, 2020
• Est. primary completion date: December 31, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subjects must be diagnosed as having possible, probable, probable-laboratory supported, or definite ALS, either sporadic or familial according to modified El Escorial criteria.

2. Age 18 or above, able to provide informed consent, and safely comply with study procedures.

3. Vital capacity (VC) of at least 50% predicted value for gender, height and age at screening visit, or in the opinion of the study physician, able to safely tolerate study procedures. (Not applicable to flexible arm)

4. Subject must be able to swallow oral medication at the Baseline Visit and expected to be able to swallow the capsules throughout the course of the study.

5. Subject must not have taken riluzole for at least 30 days, or be on a stable dose of riluzole for at least 30 days, prior to screening (riluzole-naïve participants are permitted in the study). (Not applicable to flexible arm)

6. Women must not be able to become pregnant (e.g. post menopausal, surgically sterile, or using adequate birth control) for the duration of the study and 3 months after study completion.

7. Males should practice contraception for the duration of the study and 3 months after completion.

8. Ability to safely lie flat for 90 min for PET procedures in the opinion of the study physician. (Not applicable to flexible arm)

9. High or mixed affinity to bind TSPO protein (Ala/Ala or Ala/Thr) (see section 7.2.1). (Not applicable to flexible arm)

10. Upper motor Neuron Burden (UMNB) Score =25 (out of 45) at screening visit. (Not applicable to flexible arm)

Exclusion Criteria:

1. Abnormal liver function defined as AST and/or ALT > 3 times the upper limit of the normal.

2. Renal insufficiency as defined by a serum creatinine > 1.5 times the upper limit of normal.

3. The presence of unstable psychiatric disease, cognitive impairment, or dementia that would impair ability of the participant to provide informed consent, according to PI judgment.

4. Clinically significant unstable medical condition (other than ALS) that would pose a risk to the participant if they were to participate in the study.

5. History of HIV, clinically significant chronic hepatitis, or other active infection.

6. Active inflammatory condition of autoimmune disorder (Not applicable to flexible arm)

7. Females must not be lactating or pregnant.

8. Active participation in another ALS clinical trial or exposure to an off label ALS experimental treatment within 30 days of the Baseline Visit (Not applicable to flexible arm)

9. Exposure to immunomodulatory medications within 30 days of the Baseline Visit. (Not applicable to flexible arm)

10. Any contraindication to undergo MRI studies such as

• History of a cardiac pacemaker or pacemaker wires

• Metallic particles in the body

• Vascular clips in the head

• Prosthetic heart valves

• Claustrophobia (Not applicable to flexible arm)

11. Radiation exposure that exceeds the site's current guidelines (Not applicable to flexible arm)

12. EKG finding of QTc prolongation > 450 ms for males and > 470 ms for females at screening or baseline.

13. Not on any prohibitive medication or known QT prolonging medication:

Related Conditions & MeSH terms

• Amyotrophic Lateral Sclerosis
• Motor Neuron Disease
• Sclerosis

Intervention

Drug:
• ibudilast
Ibudilast is a small molecule that crosses the blood-brain barrier after oral administration16. Its potential as a neuroprotective agent is based on in vitro and in vivo evidence of its ability to reduce microglial activation, inhibit microglia-monocyte recruitment to the central nervous system (CNS), and trigger the release of neurotrophic factors.

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	South Shore Neurologic Associates, P.C.	Patchogue	New York

Sponsors (3)

Lead Sponsor	Collaborator
MediciNova	Massachusetts General Hospital, South Shore Neurologic Associates

Country where clinical trial is conducted

United States, 

References & Publications (32)

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* Note: There are 32 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To measure the impact of MN-166 (ibudilast) on [11C]-PBR28 uptake in the motor cortices and brain stem measured by positron emission tomography (PET) imaging at 24 weeks	This is measured as the ratio of standardized uptake value (SUVR).	24 weeks
Primary	To measure the impact of MN-166 (ibudilast) on several markers of neuro-inflammation measured by blood biomarkers	Blood biomarkers for neuroinflammation include tumor necrosis factor(TNF)-alpha, interferon (IFN)-gamma, interleukin (IL)-1, IL-6, and IL-10. All blood biomarkers are measured in picrograms/milliliter (pg/mL).	36 weeks
Secondary	To evaluate the safety and tolerability of MN-166 by assessing the number of treatment-related adverse events.		36 weeks
Secondary	To evaluate the effect of ibudilast on ALS functional rating scale-revised (ALSFRS-R)	ALSFRS-R is a clinical assessment for function. It measures speech, salivation, swallowing, handwriting, cutting food and handling utensils, dressing and hygiene, turning in bed and adjusting bed clothes, walking, climbing stairs, dyspnea, orthopnea, and respiratory insufficiency. The scale ranges from 0 (no ability) to 4 (normal ability). The Total Score of these sub-assessments is the ALSFRS-R score.	36 weeks
Secondary	To evaluate the effect of ibudilast on slow vital capacity (SVC)	SVC is measured as SVC predicted liters.	36 weeks
Secondary	To evaluate the effect of ibudilast on strength as measured by Hand-held dynamometry (HHD)	HHD assesses strength and is measured in kilograms (kg).	36 weeks