Gilenya's Impact on Cognitive Function and Thalamic Volumes

NCT ID: NCT03243721

Last Updated: 2021-09-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-10-20
• Study Completion Date: 2019-11-12

Brief Summary

This evaluation will be a one-year feasibility study to characterize the neuroprotective benefits of Gilenya and its effects on cognition and grey matter volumes. The study will enroll 15 patients with relapsing-remitting multiple sclerosis being treated with Gilenya and 5 healthy controls. Each participant will undergo a battery of neurometric testing at baseline, six months, and one year. In addition, patients will undergo high-field 7T MRI at the same time points.

Detailed Description

Cognitive impairment is a well-recognized manifestation of multiple sclerosis (MS) with prevalence estimates ranging from 43 to 70%. It is also known to occur as early as the first demyelinating event and is a major factor contributing to quality of life in MS. Treatment strategies for cognitive impairment in MS are limited. Several agents have been tested as therapeutics for MS-related cognitive dysfunction and have showed no major benefit. Cognitive rehabilitation has shown some promise, but the data are limited and many studies have suffered from methodological shortcomings. Given the lack of well-established treatment options and the substantial impact of cognitive impairment, protection of cognitive function from the earliest stages of the disease is of great importance.

Cognitive outcomes received relatively little attention in the pivotal studies of MS disease modifying therapies (DMT), but some data suggest that DMT may have a positive impact on cognition. Gilenya is of special interest because it was found to have a significant protective effect on whole brain atrophy when compared against placebo and intramuscular interferon β-1a in two phase III studies, showing a 31-35% reduction in percentage brain volume change. Gilenya's effect on whole brain atrophy leads to the natural hypothesis that it may have a beneficial effect on cognitive function in MS. Also of particular interest is the extent to which protection of the thalamus and cortex contributes to Gilenya's effect on whole brain atrophy and possible effects on cognition.

The study will enroll 15 subjects from the Cleveland Clinic Mellen Center patient population. Participants must have been on Gilenya for at least 6 months at the time of study entry. The study will involve three assessments: at baseline, six months, and one year. At each time point, participants will undergo 7T MRI of the brain with and without contrast. Participants will also undergo a battery of neurometric testing at each time point. The tests will include the Brief Visuospatial Memory Test - Revised (visuospatial skills), the iPadTM Processing Speed Test (processing speed), the Selective Reminding Test (verbal learning and memory), and the Delis-Kaplan Executive Function System Sorting Test (problem-solving skills; can only be administered at baseline and one year due to version limitations).

Conditions

Multiple Sclerosis

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Gilenya treated MS patients

Multiple sclerosis patients treated with Gilenya for at least six months. This group will receive diagnostic tests: 7T MRI and Neurocognitive testing.

Group Type: EXPERIMENTAL

7T MRI

Intervention Type: DIAGNOSTIC_TEST

A high field MRI that will take approximately one hour.

Neurocognitive testing

Intervention Type: DIAGNOSTIC_TEST

A series of tests to assess memory, verbal skills, and visuospatial skills.

Healthy controls

Subjects without multiple sclerosis or other diseases of the central nervous system. This group will receive diagnostic tests: 7T MRI and Neurocognitive testing.

Group Type: EXPERIMENTAL

7T MRI

Intervention Type: DIAGNOSTIC_TEST

A high field MRI that will take approximately one hour.

Neurocognitive testing

Intervention Type: DIAGNOSTIC_TEST

A series of tests to assess memory, verbal skills, and visuospatial skills.

Interventions

7T MRI

A high field MRI that will take approximately one hour.

Intervention Type: DIAGNOSTIC_TEST

Neurocognitive testing

A series of tests to assess memory, verbal skills, and visuospatial skills.

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

1. RRMS phenotype

2. Treated with Gilenya for ≥6 months at the time of the baseline visit.

3. Age 18-50 inclusive.

4. EDSS 0-4.0

5. Disease duration of 5-15 years.

6. At least 12 years of education (high school diploma or general equivalency diploma).

7. Physically capable of completing neurometric testing and MRI studies.

1. Age 18-50 inclusive.

2. At least 12 years of education (high school diploma or general equivalency diploma)

3. Physically capable of completing neurometric testing and MRI studies.

Exclusion Criteria

1. Contraindication to MRI (e.g. metal implants)

2. Current use of immunomodulatory or immunosuppressant medications other than Gilenya.

3. Disease of the central nervous system other than MS (e.g. Alzheimer disease, stroke, epilepsy).

4. Use of anti-psychotic or psychostimulant medications. Patients started on modafinil or armodafinil more than six months prior to enrollment will not be excluded.

5. Ongoing major depressive disorder that, in the opinion of the investigator, may affect cognitive functioning.

6. MS relapse within 90 days of study entry.

7. Treatment with corticosteroids within 90 days of study entry.

8. Current illicit substance use.

9. History of alcohol or drug abuse.

1. Contraindication to MRI (e.g. metal implants, claustrophobia).

2. Disease of the central nervous system (e.g. MS, Alzheimer disease, stroke, epilepsy).

3. Use of anti-psychotic or psychostimulant medications. Patients started on modafinil or armodafinil more than six months ago will not be excluded.

4. Ongoing major depressive disorder that, in the opinion of the investigator, may affect cognitive functioning.

5. Current illicit substance use.

6. History of alcohol or drug abuse.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Novartis Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

The Cleveland Clinic

OTHER

Sponsor Role: lead

Responsible Party

Devon Conway MD

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Devon S Conway, MD

Role: PRINCIPAL_INVESTIGATOR

The Cleveland Clinic

Locations

Cleveland Clinic Foundation

Cleveland, Ohio, United States

Countries

United States

Other Identifiers

CCF 17-766

Identifier Type: -

Identifier Source: org_study_id