Combination of Antidepressants and Fingolimod Relapsing-remitting Multiple Sclerosis (RRMS) Patients With Depression (REGAIN)
This study is currently recruiting participants.
Verified February 2013 by Novartis
Sponsor:
Novartis Pharmaceuticals
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )
ClinicalTrials.gov Identifier:
NCT01436643
First received: September 16, 2011
Last updated: February 7, 2013
Last verified: February 2013
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Purpose
This is a prospective, multi-center, open-label study in Relapsing-remitting Multiple Sclerosis (RRMS) patients with mild to moderate depression treated with selected serotonin reuptake inhibitors (SSRI) or serotonin and norepinephrine reuptake inhibitors (SNRI) antidepressants over 16 weeks as add-on to fingolimod treatment. It is designed to evaluate the safety and tolerability of this combination in this patient population based on an immunomodulatory treatment with fingolimod.
| Condition | Intervention | Phase |
|---|---|---|
|
Depression Relapsing-remitting Multiple Sclerosis |
Drug: Fingolimod plus Venlafaxine Drug: Fingolimod plus Citalopram Drug: Fingolimod plus Fluoxetine Drug: Fingolimod plus Sertraline |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A 21-week, Multicenter, Open Label Study to Evaluate the Safety and Tolerability Profile of the Combination of a SSRI or SNRI Antidepressive Therapy With Oral Fingolimod in the Treatment of RRMS Patients With Mild to Moderate Depression |
Resource links provided by NLM:
Genetics Home Reference related topics:
multiple sclerosis
Drug Information available for:
Fluoxetine
Fluoxetine hydrochloride
Citalopram hydrobromide
Citalopram
Sertraline hydrochloride
Sertraline
Venlafaxine
Venlafaxine hydrochloride
Fingolimod
Fingolimod hydrochloride
Escitalopram oxalate
U.S. FDA Resources
Further study details as provided by Novartis:
Primary Outcome Measures:
- Safety and tolerability profile of the combination therapy of an antidepressant type SSRI or SNRI with oral fingolimod with respect to adverse events and laboratory parameters [ Time Frame: 18 weeks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 500 |
| Study Start Date: | November 2011 |
| Estimated Study Completion Date: | May 2013 |
| Estimated Primary Completion Date: | May 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Fingolimod plus Citalopram | Drug: Fingolimod plus Citalopram |
| Experimental: Fingolimod plus Fluoxetine | Drug: Fingolimod plus Fluoxetine |
| Experimental: Fingolimod plus Sertraline | Drug: Fingolimod plus Sertraline |
| Experimental: Fingolimod plus Venlafaxine | Drug: Fingolimod plus Venlafaxine |
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Subjects with relapsing remitting MS defined by 2010 revised McDonald criteria (see Appendix 4)
- Patients with Expanded Disability Status Scale (EDSS) score of 0-6.5 (see Appendix 8)
- 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)
- Depression according to ICD-10 criteria
- Mild-moderate depression assessed by BDI-II score between 14-28 inclusively measured before study inclusion and before fingolimod is administered
Exclusion Criteria:
- Patients with a history of chronic disease of the immune system other than MS which requires systemic immunosuppressive treatment, or a known immunodeficiency syndrome. Patients with Crohns disease or ulcerative colitis are excluded without exception
- History or presence of malignancy (other than localized basal or squamous cell carcinoma of the skin)
- 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 Screening
- 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 start of fingolimod
- Patients who are or have been treated with:
- immunoglobulins and/or monoclonal antibodies (including natalizumab) within 3 months prior to start of fingolimod
- Systemically applied corticosteroids or adrenocorticotropic hormones (ACTH) within 1 month prior to start of fingolimod (nevertheless, topical application is permitted);
- Immunosuppressive medications such as azathioprine or methotrexate, within 3 months prior to start of fingolimod;
- Cyclophosphamid and mitoxantrone within 6 months prior to start of fingolimod
- cladribine at any time
- current psychological or pharmacological treatment for depression (MAO inhibitors in particular), a washout period of 1 month prior start of fingolimod is required
- current treatment with linezolid, a washout period of 1 month prior start of fingolimod is required
Other protocol-defined inclusion/exclusion criteria may apply
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01436643
Hide Study Locations
Contacts
| Contact: Novartis Pharmaceuticals | 862-778-8300 |
Hide Study LocationsLocations
| Germany | |
| Novartis Investigative Site | Recruiting |
| Ostfildern, Baden-Wuerttemberg, Germany, 73760 | |
| Novartis Investigative Site | Recruiting |
| Achim, Germany, 28832 | |
| Novartis Investigative Site | Recruiting |
| Altenholz-Stift, Germany, 24161 | |
| Novartis Investigative Site | Recruiting |
| Aschaffenburg, Germany, 63739 | |
| Novartis Investigative Site | Recruiting |
| Augsburg, Germany, 86156 | |
| Novartis Investigative Site | Recruiting |
| Bad Honnef, Germany, 53604 | |
| Novartis Investigative Site | Recruiting |
| Bad Saarow, Germany, 15526 | |
| Novartis Investigative Site | Recruiting |
| Baesweiler, Germany, 52499 | |
| Novartis Investigative Site | Recruiting |
| Bayreuth, Germany, 95445 | |
| Novartis Investigative Site | Recruiting |
| Berlin, Germany, 13439 | |
| Novartis Investigative Site | Not yet recruiting |
| Berlin, Germany, 10961 | |
| Novartis Investigative Site | Recruiting |
| Berlin, Germany, 10437 | |
| Novartis Investigative Site | Recruiting |
| Berlin, Germany, 10625 | |
| Novartis Investigative Site | Recruiting |
| Berlin, Germany, 12165 | |
| Novartis Investigative Site | Recruiting |
| Berlin, Germany, 13347 | |
| Novartis Investigative Site | Recruiting |
| Berlin, Germany, 12621 | |
| Novartis Investigative Site | Recruiting |
| Berlin, Germany, 12163 | |
| Novartis Investigative Site | Not yet recruiting |
| Berlin, Germany, 14057 | |
| Novartis Investigative Site | Recruiting |
| Bielefeld, Germany, 33602 | |
| Novartis Investigative Site | Recruiting |
| Bielefeld, Germany, 33647 | |
| Novartis Investigative Site | Recruiting |
| Bochum, Germany, 44787 | |
| Novartis Investigative Site | Completed |
| Bochum, Germany, 44892 | |
| Novartis Investigative Site | Recruiting |
| Bremerhaven, Germany, 27574 | |
| Novartis Investigative Site | Recruiting |
| Buchholz, Germany, 21244 | |
| Novartis Investigative Site | Recruiting |
| Butzbach, Germany, 35510 | |
| Novartis Investigative Site | Recruiting |
| Dresden, Germany, 01307 | |
| Novartis Investigative Site | Not yet recruiting |
| Dresden, Germany, 01067 | |
| Novartis Investigative Site | Recruiting |
| Erfurt, Germany, 99089 | |
| Novartis Investigative Site | Recruiting |
| Essen, Germany, 45138 | |
| Novartis Investigative Site | Completed |
| Essen, Germany, 45134 | |
| Novartis Investigative Site | Completed |
| Essen, Germany, 45147 | |
| Novartis Investigative Site | Not yet recruiting |
| Gelsenkirchen, Germany, 45879 | |
| Novartis Investigative Site | Recruiting |
| Grevenbroich, Germany, 41515 | |
| Novartis Investigative Site | Not yet recruiting |
| Göttingen, Germany, 37073 | |
| Novartis Investigative Site | Recruiting |
| Hamburg, Germany, 22083 | |
| Novartis Investigative Site | Completed |
| Hamburg, Germany, 20099 | |
| Novartis Investigative Site | Recruiting |
| Hamburg, Germany, 22179 | |
| Novartis Investigative Site | Recruiting |
| Hannover, Germany, 30167 | |
| Novartis Investigative Site | Recruiting |
| Heidenheim, Germany, 89518 | |
| Novartis Investigative Site | Withdrawn |
| Ingolstadt, Germany, 85049 | |
| Novartis Investigative Site | Recruiting |
| Kastellaun, Germany, 56288 | |
| Novartis Investigative Site | Withdrawn |
| Kiel, Germany, 24105 | |
| Novartis Investigative Site | Recruiting |
| Klingenmünster, Germany, 76889 | |
| Novartis Investigative Site | Recruiting |
| Königsbrück, Germany, 01936 | |
| Novartis Investigative Site | Completed |
| Ladenburg, Germany, 68526 | |
| Novartis Investigative Site | Withdrawn |
| Landshut, Germany, 84028 | |
| Novartis Investigative Site | Completed |
| Leipzig, Germany, 04157 | |
| Novartis Investigative Site | Recruiting |
| Leipzig, Germany, 04275 | |
| Novartis Investigative Site | Recruiting |
| Lohr am Main, Germany, 79816 | |
| Novartis Investigative Site | Completed |
| Ludwigshafen, Germany, 67063 | |
| Novartis Investigative Site | Not yet recruiting |
| Lüdenscheid, Germany, 58511 | |
| Novartis Investigative Site | Recruiting |
| Mannheim, Germany, 68159 | |
| Novartis Investigative Site | Recruiting |
| Merzig, Germany, 66663 | |
| Novartis Investigative Site | Recruiting |
| München, Germany, 81829 | |
| Novartis Investigative Site | Recruiting |
| Münster, Germany, 48147 | |
| Novartis Investigative Site | Recruiting |
| Nienburg, Germany, 31582 | |
| Novartis Investigative Site | Recruiting |
| Nümbrecht, Germany, 51588 | |
| Novartis Investigative Site | Recruiting |
| Oberhausen, Germany, 46045 | |
| Novartis Investigative Site | Recruiting |
| Oldenburg, Germany, 26122 | |
| Novartis Investigative Site | Recruiting |
| Potsdam, Germany, 14471 | |
| Novartis Investigative Site | Recruiting |
| Schwalmstadt-Treysa, Germany, 34613 | |
| Novartis Investigative Site | Completed |
| Schwerin, Germany, 19057 | |
| Novartis Investigative Site | Completed |
| Seelow, Germany, 15306 | |
| Novartis Investigative Site | Not yet recruiting |
| Siegen, Germany, 57072 | |
| Novartis Investigative Site | Recruiting |
| Sinsheim, Germany, 74889 | |
| Novartis Investigative Site | Recruiting |
| Stadtroda, Germany, 07646 | |
| Novartis Investigative Site | Not yet recruiting |
| Stralsund, Germany, D-18435 | |
| Novartis Investigative Site | Recruiting |
| Stuttgart, Germany, 70191 | |
| Novartis Investigative Site | Recruiting |
| Stuttgart, Germany, 70182 | |
| Novartis Investigative Site | Recruiting |
| Telgte, Germany, 48291 | |
| Novartis Investigative Site | Recruiting |
| Tübingen, Germany, 72076 | |
| Novartis Investigative Site | Recruiting |
| Weil am Rhein, Germany, 79576 | |
| Novartis Investigative Site | Recruiting |
| Wermsdorf, Germany, 04779 | |
| Novartis Investigative Site | Completed |
| Wolfratshausen, Germany, 82515 | |
| Novartis Investigative Site | Recruiting |
| Zwickau, Germany, 08060 | |
Sponsors and Collaborators
Novartis Pharmaceuticals
Investigators
| Study Director: | Novartis Pharmaceuticals | Novartis Pharmaceuticals |
More Information
No publications provided
| Responsible Party: | Novartis ( Novartis Pharmaceuticals ) |
| ClinicalTrials.gov Identifier: | NCT01436643 History of Changes |
| Other Study ID Numbers: | CFTY720DDE06, 2011-001692-39 |
| Study First Received: | September 16, 2011 |
| Last Updated: | February 7, 2013 |
| Health Authority: | United States: Food and Drug Administration Germany: Federal Institute for Drugs and Medical Devices |
Keywords provided by Novartis:
|
Depression Multiple Sclerosis Fingolimod Venlafaxine |
Fluoxetine Sertraline Citalopram |
Additional relevant MeSH terms:
|
Depression Depressive Disorder Multiple Sclerosis Sclerosis Multiple Sclerosis, Relapsing-Remitting Behavioral Symptoms Mood Disorders Mental Disorders Demyelinating Autoimmune Diseases, CNS Autoimmune Diseases of the Nervous System Nervous System Diseases Demyelinating Diseases Autoimmune Diseases Immune System Diseases Pathologic Processes |
Antidepressive Agents Citalopram Fluoxetine Sertraline Venlafaxine Dexetimide Fingolimod Psychotropic Drugs Central Nervous System Agents Therapeutic Uses Pharmacologic Actions Antidepressive Agents, Second-Generation Serotonin Uptake Inhibitors Neurotransmitter Uptake Inhibitors Neurotransmitter Agents |
ClinicalTrials.gov processed this record on May 19, 2013