A Non-randomized, Exploratory, Study to Assess Clinical Response to Gilenya® (Fingolimod) in a Cohort of Relapsing Remitting Hispanic MS Forms
| City: |
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Los Angeles |
| State: |
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California |
| Zip Code: |
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90033 |
| Conditions: |
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Multiple Sclerosis |
| Purpose: |
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Gilenya (fingolimod) is approved for multiple sclerosis. However, it is unclear of its
clinical effect in the Hispanics with MS given that clinical studies had limited
representation of this population. It is also unclear if Gilenya would be as effective in
individuals with disease predominantly affecting the optic nerve and spinal cord (OSMS)
commonly seen in Asian populations.
Objectives: To compare the clinical response of Gilenya® (fingolimod) in relapsing
remitting OSMS and MS of Hispanic descent using ancestral markers as a biomarker of
treatment response and clinical disease state.
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| Study Summary: |
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The primary objective of this study is to determine the success of Gilenya® (fingolimod)
treatment in patients with MS of Hispanic descent relative to their ancestral background.
Therapeutic success will be determined by annualized relapse rate (ARR; defined as the
number of relapses divided by the person years followed) after initiation of treatment with
Gilenya® (fingolimod)in comparison to the relapse rate in the previous 12 months. This will
be determined based on medical chart extraction, in-person assessment and regular clinical
follow-up.
A secondary objective of this study is to investigate whether the efficacy of Gilenya®
(fingolimod) is superior or equal in HW which have higher loads of Amerindian versus
Caucasian background with opticospinal MS (OSMS-NMO neg) versus classical MS (CMS) in the
first 12 months using radiological and clinical parameters. The following measures will be
obtained:
1. Number of relapse-free patients over the investigational period
2. Site of relapse defined as brain or spinal cord.
3. Sustained Disability progression will be defined as a one point (1) increase from
baseline in patients with baseline EDSS score from 0 to 5.0; or half a point (0.5)
increase in patients with baseline EDSS score of 5-5.5 or above after 3 months.
4. MRI changes as described as number of new T2 lesions and number of Gd-enhancing lesions
after 12 months from baseline.
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| Criteria: |
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Inclusion Criteria:
- Clinically definite multiple sclerosis defined by McDonald Criteria (8) with a score
of 0 to 5.5 on the Expanded Disability Status Scale (EDSS)(9). Inclusion will also be
determined by PI if clinically indicated. Relapsing remitting form of MS.
- Between 18-65 years of age (This age range is selected so as to capture the vast
majority of patients who are seen in the clinics with a confirmed diagnosed of MS.
This age range also allows for exclusion of co-morbid conditions that may be
associated with aging as well as pediatric cases where their disease characteristics
have been shown to be different).
- Ability to understand and sign the IRB-approved informed consent form prior to the
performance of any study-specific procedures and is willing to comply with the
required scheduling and assessments of the protocol.
- Women of childbearing potential must have a negative urine pregnancy test at the
Screening Visit and must be willing to practice a reliable birth-control method.
- Patient must be willing to discontinue and remain free from concomitant
immunosuppressive or additional immunomodulatory treatment (including IFNβ1a, 1b,
natalizumab and GA) for the duration of the study.
- Willing to answer a series of questions about disease, ancestry, residence history,
socioeconomic status and ethnic background.
- Willing to donate 50cc of blood for genetic admixture and immunological testing on
three occasions (O months, 6 months, 12 months).
- Willing to undergo MRI as standard of care at a 1.5 Tesla magnet strength at least.
Exclusion Criteria:
- Inability to understand nature of the study.
- Lack of a definite diagnosis of Multiple Sclerosis such as clinical isolated syndrome
will be excluded.
- NMO Antibody positive.
- Primary progressive or secondary progressive MS.
- Inability to undergo an MRI study or receive contrast agent and GFR<30.
- Considered by the Investigator to be immunocompromised, based on medical history,
physical examination, or laboratory testing or due to prior immunosuppressive
treatment.
- Lack of Varicella immunity.
- History of, or available abnormal laboratory results indicative of, any significant
cardiac, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic,
pulmonary, gastrointestinal, dermatologic, psychiatric (including major depression),
renal, and/or other major disease.
- History of malignancy (subjects with basal cell carcinoma that has been completely
excised prior to study entry remain eligible).
- Known history of human immunodeficiency virus infection, hematological malignancy, or
organ transplantation, history of severe allergic or anaphylactic reactions or known
drug hypersensitivity.
- Prior treatment history with the interferons, glatiramer acetate or natalizumab will
be acceptable after drug clearance of 1 month. 1 month has been selected due to
clinical experience of possible disease breakthrough if longer period is performed.
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| NCT ID: |
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NCT01592097 |
| Primary Contact: |
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Principal Investigator
Lilyana Amezcua, MD
University of Southern California
Pat Gutierrez
Phone: 323-342-6817
Email: fgutierr@usc.edu
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| Backup Contact: |
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Email: joseapar@usc.edu
Jose Aparicio
Phone: 323-442-6833
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| Location Contact: |
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Los Angeles, California 90033
United States
Pat Gutierrez
Phone: 323-442-6817
Email: fgutierr@usc.edu
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 17, 2013 |
| Modifications to this listing: |
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