Long-term Effect of Fingolimod on Circulating Immunocompetent Mononuclear Cells in Patients With Multiple Sclerosis

NCT01755871 | Terminated Phase 4

• 1 other identifier: FINGOHHU
• Study Type: interventional
• Target: 8
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to explore immunomodulatory and immunosuppressive mechanisms of action of fingolimod in patients with Relapsing remitting multiple Sclerosis to collect data on biomarkers after initiation of fingolimod treatment.

Conditions

Relapsing Remitting Multiple Sclerosis

Outcome Measures

Primary Outcomes (1)

• Reduction of CD4+ and CD8+ naïve T cells (CCR7+ CD45RA+) and central memory T cells (CCR7+CD45RA-), and an elevation of effector memory T cells (CCR7- CD45RA-) by examining the blood

  The primary endpoints are the reduction of CD4+ and CD8+ naïve T cells (CCR7+ CD45RA+) and central memory T cells (CCR7+CD45RA-), and an elevation of effector memory T cells (CCR7- CD45RA-)in the blood, and to study the effect of Fingolimod on Th17 cells by studying their signature cytokines (IL-17, IL-21, IL-22) as well as signature transcription factors (ROR-gamma-t, ROR-alpha, STAT3, Runx1) in peripheral venous blood over 2 years versus baseline.

  Day 0, Day 28, Day 84, Day 168, Day 336, Day 504, Day 672 after treatment

Secondary Outcomes (1)

• To investigate changes from baseline in B Lymphocytes, monocytes and NK cells in the blood after treatment with fingolimod

  Day 0, Day 28, Day 84, Day 168, Day 336, Day 504, Day 672 after treatment

Other Outcomes (1)

• Change of the biomarkers BDNF, NGF, CNTF and LIF in the blood during treatment with fingolimod

  Day 0, Day 28, Day 84, Day 168, Day 336, Day 504, Day 672 after treatment

Study Arms (1)

Fingolimod

EXPERIMENTAL

Gilenya 0,5mg per day, oral

Drug: Fingolimod

Interventions

Fingolimod DRUG

0,5mg Fingolimod once a day

Also known as: Gilenya

Fingolimod

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Written informed consent from patients capable of giving or withholding full informed consent must be obtained before any assessment is performed in this trial.
• Male or female subjects aged 18-65 years.
• Subjects with relapsing remitting forms of MS defined by 2010 revised McDonald criteria (see Appendix).
• Patients with high disease activity despite treatment with a disease modifying therapy (≥ 1 relapse in the previous year, ≥ 9 hyperintense T2 lesions or ≥1 Gd-enhancing lesion or "non-responding" which could be defined as unchanged or increased relapse rate or ongoing severe relapses compared to previous year) or patients with rapidly evolving severe RRMS (e.g. ≥ 2 relapses with disease progression in one year and ≥ 1 Gd-enhancing lesion or with a significant increase in T2 lesions compared to a recent MRI).
• Patients with Expanded Disability Status Scale (EDSS) score of 0-6.5 (see Appendix).
• Sufficient ability to read, write, communicate and understand

You may not qualify if:

• Patients with a manifestation of MS other than relapsing remitting MS.
• Patients with a history of chronic disease of the immune system other than MS, which requires systemic immunosuppressive treatment, or a known immunodeficiency syndrome.
• History or presence of malignancy (other than localized basal cell carcinoma of the skin and carcinoma in situ of the cervix) in the last 5 years
• Diabetic patients with moderate or severe non-proliferative diabetic retinopathy or proliferative diabetic retinopathy and uncontrolled diabetic patients with HbA1c \> 7%.
• Diagnosis of macular edema during Baseline Visit (patients with a history of macular edema will be allowed to enter the study provided that they do not have macular edema at the ophthalmic baseline visit).
• Patients with active systemic bacterial, viral or fungal infections, or known to have AIDS, Hepatitis B, Hepatitis C infection or to have positive HIV antibody, Hepatitis B surface antigen or Hepatitis C antibody tests.
• Negative for varicella-zoster virus IgG antibodies at Baseline.
• Have received any live or live attenuated vaccines (including for varicella-zoster virus or measles) within 1 month prior to baseline.
• Patients who have received total lymphoid irradiation or bone marrow transplantation.
• Patients who expect to be treated with any disease modifying drugs (DMD) during the study (i.e. IFN-β, glatiramer acetate); however no washout is needed for DMDs prior to baseline.

Sponsors & Collaborators

• Heinrich-Heine University, Duesseldorf: lead
• Novartis Pharmaceuticals: collaborator

Study Sites (1)

Heinrich Heine Universität Düsseldorf

Düsseldorf, Nord-Rhein Westfahlen, 40225, Germany

Location

MeSH Terms

Conditions

Multiple Sclerosis, Relapsing-Remitting

Interventions

Fingolimod Hydrochloride

Condition Hierarchy (Ancestors)

Multiple Sclerosis; Demyelinating Autoimmune Diseases, CNS; Autoimmune Diseases of the Nervous System; Nervous System Diseases; Demyelinating Diseases; Autoimmune Diseases; Immune System Diseases

Intervention Hierarchy (Ancestors)

Sphingosine; Amino Alcohols; Alcohols; Organic Chemicals; Propylene Glycols; Glycols; Amines

Study Officials

• Bernd Kieseier, Prof.

  Heinrich Heine Universität Düsseldorf

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 4
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 19, 2012
• First Posted: December 24, 2012
• Study Start: January 1, 2013
• Primary Completion: January 1, 2016
• Study Completion: February 1, 2016
• Last Updated: June 9, 2016

Record last verified: 2015-06

Locations

DE (1)