Ofatumumab Subcutaneous Administration in Subjects With Relapsing-Remitting Multiple Sclerosis (MIRROR)

• ClinicalTrials.gov Identifier: NCT01457924
• Recruitment Status: Completed
• First Posted: October 24, 2011
• Results First Posted: March 1, 2018
• Last Update Posted: June 6, 2018
• Sponsor: GlaxoSmithKline
• Information provided by (Responsible Party): GlaxoSmithKline

Study Description

Brief Summary:

Ofatumumab is a novel Immunoglobulin 1ĸ ( IgG1ĸ) lytic monoclonal antibody (mAb) that specifically binds to the human Cluster of Differentiation 20 (CD20) antigen of which expression is restricted to B lymphocytes from the pre-B cell stage to the plasmacytoid immunoblast stage only. A recent trial with an anti-CD20 mAb (rituximab) demonstrated that targeting B-cells reduces the number of gadolinium-enhancing (GdE) T1 lesions and the relapse rate in relapsing-remitting multiple sclerosis (RRMS). Ofatumumab has been shown to be both well tolerated and efficacious in several indications, including a small, placebo-controlled trial in RRMS using an intravenous (IV) formulation.

This double-blind, placebo-controlled, parallel-group study will investigate the safety and efficacy of a subcutaneous formulation of ofatumumab in the treatment of subjects with RRMS. The primary objective of the study is to investigate the efficacy as assessed by magnetic resonance imaging. Other objectives will include evaluation of tolerability/safety, dose-response relationship, pharmacokinetics, pharmacodynamics, exposure-response, as well as other clinical endpoints.

Condition or disease	Intervention/treatment	Phase
Multiple Sclerosis	Drug: Ofatumumab 3mg; Drug: Ofatumumab 30mg; Drug: Ofatumumab 60mg; Drug: Placebo	Phase 2

Detailed Description:

Ofatumumab is a novel immunoglobulin G (IgG) 1ĸ lytic monoclonal antibody (mAb) that specifically binds to the human CD20 antigen of which expression is restricted to B lymphocytes from the pre-B cell stage to the plasmacytoid immunoblast stage only. A recent trial with rituximab demonstrated that targeting B-cells reduces the number of gadolinium-enhancing (GdE) T1 lesions and the relapse rate in Relapsing-Remitting Multiple Sclerosis (RRMS). The intravenous (IV) formulation of ofatumumab has been shown to be both well-tolerated and efficacious in Phase I/II & III clinical trials within in B-cell Chronic Lymphocytic Leukemia (B-CLL), non-Hodgkin's Follicular Lymphoma (FL), and active Rheumatoid Arthritis (RA). A Phase II study of ofatumumab in Relapsing Remitting Multiple Sclerosis (RRMS) subjects, OMS115102 (also known as Study GEN414) is ongoing as of the development of this protocol. The primary objective of the OMS115102 protocol was to investigate the safety of a range of doses (100mg, 300 mg, and 700 mg) of ofatumumab in RRMS subjects, using an IV formulation. The treatment period for OMS115102 has been completed; there are currently 4 subjects ongoing in the Individualized Follow up Phase. In the Week 0 to 24 period the majority of subject who were exposed to active treatment with ofatumumab (active/placebo) had Cluster of Differentiation 19 (CD19+) and CD20+ levels that were suppressed to zero; recovery started for the 100 mg and 300 mg active/placebo groups, at approximately, 12 and 20 weeks after discontinuation of dosing with ofatumumab, respectively. In the 700 mg active/placebo group, all but one subject had a persistent and complete CD19+ suppression at Week 24. In the Week 24 to 48 period, when those who had previously been exposed to placebo were treated with ofatumumab (placebo/active), the majority of the subjects treated with ofatumumab had CD19+ and CD20+ cell levels suppressed to zero (mm3) within one week. Recovery started for the subjects in the 100 mg placebo/active group after approximately 16 weeks (from these subjects' first infusion). In the 300 mg and 700 mg placebo/active groups, all subjects except one (700 mg) had persistent and complete CD19+ suppression at Week 48.

This study will evaluate the magnetic resonance imaging (MRI) efficacy and will investigate the safety of ofatumumab using a subcutaneous (SQ) formulation in subjects with RRMS. This Phase II study will be a multi-center, randomized, double-blind, placebo-controlled, dose ranging study in subjects with RRMS. Randomization will be stratified based on the absence or presence of GdE brain lesions present at screening. The core 54 week period of the study is made up of an up to 6-week Screening Phase, a 24-week Treatment Phase, and a 24-week Follow-up Phase. Subjects will attend the clinic a total of approximately twelve times (including Screening) during this core 54-week period of the study. Subjects who have remained enrolled and participate in the study from Screening though the end of the 24-Week Follow-Up Period (Week 48 Visit) will be considered completers. Upon completion or withdrawal from the core study period, subjects will be followed in the Individualized Follow-up Phase. Subjects will return to the clinic every 12 weeks for a B-cell count and other safety assessments. Subjects will remain in Individualized Follow-up (IFU) until CD19+ B-lymphocyte counts recover to LLN or baseline (if <LLN);OR if B-cell counts have not recovered by the Week 120 visit (100 weeks after the last possible treatment dose at Week 20), until either the B-cell counts or circulating IgG are >LLN or baseline levels (if <LLN). Male and female subjects with a diagnosis of RRMS will be screened for eligibility for the study. All non-MRI screening procedures should generally be completed within 14 days of informed consent being given. To the extent possible, investigators are to verify subjects meet all non MRI-related entry criteria before performing screening MRIs. Subjects who meet all inclusion and exclusion criteria will be centrally randomized into the study at the Baseline Visit (Week 0) to receive one of the following treatment arms: SQ administration of ofatumumab 3 mg, 30 mg, or 60 mg every 12 weeks, 60 mg every 4 weeks, or placebo. Half of the subjects randomized to the 30 mg group, or to either of the 60 mg groups, will receive a 3 mg conditioning dose at Week 0. Based on tolerability observed in other indications, the 3 mg conditioning dose may produce a more gradual lysis of B-cells, thereby reducing the cytokine release reactions to the initial 30 mg or 60 mg dose and potentially improve tolerability for subjects. The Treatment Phase lasts for 24 weeks and the subject will be seen 8 times during this phase. Upon completion or discontinuation of the Treatment Phase, subjects will enter a 24-week Follow-up Phase, during which they will not receive investigational product. Ideally, no other MS disease-modifying therapies should be taken during this period in order to allow for a clean analysis of safety data and the potential for Cluster of Differentiation (CD)+19 B-lymphocyte cell and immunoglobulin normalization to be assessed. However, if the start of a MS disease-modifying therapy is considered medically necessary, follow up will continue through the completion of the 24-Week Follow-up Phase. The subject will then be withdrawn from the study, and will not enter into the Individualized Follow-up Phase. Upon completion of the 24-Week Follow-up Phase, all subjects who have not started an MS disease modifying therapy (DMT) will enter the Individualized Follow up. During this Phase, subjects will return to the clinic every 12 weeks for a B-cell count and other safety assessments. If a subject starts a MS DMT during this follow-up phase they will be withdrawn from the study. To the extent possible, subjects experiencing a relapse during the study should return immediately to the clinic for evaluation. All MRI scans will be sent to a central reader for analysis. An Independent Data Monitoring Committee (IDMC) will evaluate risks relative to benefits through review of safety and efficacy information on an ongoing basis during the study. Approximately 245 subjects will be screened to provide around 196 subjects for randomization into the study. Assuming an attrition rate of 10% between the baseline visit and the six-month treatment visit, this will provide approximately 176 evaluable subjects.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 232 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: A Randomized, Double-blind, Placebo-controlled, Parallel-Group, Dose-Ranging Study to Investigate the MRI Efficacy and Safety of Six Months' Administration of Ofatumumab in Subjects With Relapsing-Remitting Multiple Sclerosis (RRMS)
• Study Start Date: November 1, 2011
• Actual Primary Completion Date: August 23, 2013
• Actual Study Completion Date: June 10, 2015

Arms and Interventions

Arm	Intervention/treatment
Experimental: Cohort 1; Placebo and one dose of Ofatumumab 3mg over 24 weeks	Drug: Ofatumumab 3mg; 3mg of investigational product; Drug: Placebo; Placebo
Experimental: Cohort 2; Two doses of Ofatumumab 3mg over 24 weeks	Drug: Ofatumumab 3mg; 3mg of investigational product; Drug: Placebo; Placebo
Experimental: Cohort 3.1; Two doses of Ofatumumab 30mg over 24 weeks	Drug: Ofatumumab 30mg; 30mg of investigational product; Drug: Placebo; Placebo
Experimental: Cohort 3.2; Conditioning dose of Ofatumumab 3mg at randomization, two doses of Ofatumumab 30mg over 24 weeks	Drug: Ofatumumab 3mg; 3mg of investigational product; Drug: Ofatumumab 30mg; 30mg of investigational product; Drug: Placebo; Placebo
Experimental: Cohort 4.1; Two doses of Ofatumumab 60mg over 24 weeks	Drug: Ofatumumab 60mg; 60mg of investigational product; Drug: Placebo; Placebo
Experimental: Cohort 4.2; Conditioning dose of Ofatumumab 3mg at randomization, two doses of Ofatumumab 60mg over 24 weeks	Drug: Ofatumumab 3mg; 3mg of investigational product; Drug: Ofatumumab 60mg; 60mg of investigational product; Drug: Placebo; Placebo
Experimental: Cohort 5.1; Six doses of Ofatumumab 60mg over 24 weeks	Drug: Ofatumumab 60mg; 60mg of investigational product; Drug: Placebo; Placebo
Experimental: Cohort 5.2; Conditioning dose of Ofatumumab 3mg at randomization, six doses of Ofatumumab 60mg over 24 weeks	Drug: Ofatumumab 3mg; 3mg of investigational product; Drug: Ofatumumab 60mg; 60mg of investigational product

Outcome Measures

Primary Outcome Measures :

1. Cumulative Number of New Gadolinium-enhancing (GdE) T1 Lesions at Week 12 [ Time Frame: Week 12 ]
   The cumulative number of new GdE T1 lesion at Week 12 were analyzed from screening based on magnetic resonance imaging (MRI) brain scans at Weeks 4, 8, and 12. The outcome measure was analyzed using an Emax model adjusting for the presence/absence of GdE lesions on the Screening MRI and assuming the number of new lesions followed a negative binomial distribution. Dose was fitted as a continuous variable. The number of scans contributing to the cumulative number of lesions was fitted as an offset. Estimates of the rate of cumulative number of new GdE lesions per scan at Week 12 were determined from the model. The all evaluable scans (AES) dataset was used which included all evaluable on-treatment MRI scans for each participant analysed.

Secondary Outcome Measures :

1. Cumulative Number of New GdE T1 Lesions at Week 24 [ Time Frame: Week 24 ]
   The cumulative number of new GdE T1 lesion at Week 24 were analyzed from screen based on MRI brain scans at Weeks 4, 8, 12, 16, 20 and 24. Anticipating an underlying negative binomial distribution with a log-link function, adjusted for treatment and presence/absence of GdE lesions on the Screening MRI. Treatment group was fitted as a categorical variable. The number of scans contributing to the cumulative number of lesions was fitted as an offset. Estimates of the rate of cumulative number of new GdE T1 lesions per scan at Week 24 were determined from the model. The AES dataset was used which included all evaluable on-treatment MRI scans for each participant analyzed.
2. Change From Baseline in Brain Volume at Week 24 and Week 48 [ Time Frame: Baseline (Week 0), Week 24 and Week 48 ]
   Brain volume is a measure of brain size determined by a MRI scan. Baseline is defined as the par. last available assessment prior to initiation of the IP (i.e. Screening). Change from Baseline was calculated by subtracting the Baseline value from the post-Baseline value.
3. Cumulative Number of Persistent GdE Brain Lesions on T1-weighted MRI at Week 12 [ Time Frame: Week 12 ]
   The cumulative number of persistent GdE T1 lesions at Week 12 were analyzed from screen based on MRI scans at Weeks 4, 8, and 12. The AES dataset was used which included all evaluable on-treatment MRI scans for each par. analyzed.
4. Cumulative Number of All (New Plus Persistent) GdE Brain Lesions on T1-weighted MRI at Week 12 [ Time Frame: Week 12 ]
   The cumulative number of all (new plus persistent) GdE T1 lesion at Week 12 were analyzed from screen based on MRI brain scans at Weeks 4, 8 and 12. Anticipating an underlying negative binomial distribution with a log-link function, adjusted for treatment and presence/absence of GdE lesions on the Screening MRI. Treatment group was fitted as a categorical variable. The number of scans contributing to the cumulative number of lesions was fitted as an offset. Estimates of the rate of cumulative number of all (new plus persistent) GdE T1 lesions per scan at Week 12 were determined from the model. The AES dataset was used which included all evaluable on-treatment MRI scans for each par. analyzed.
5. Total Volume of New GdE Brain Lesions on T1-weighted MRI at Week 12 [ Time Frame: Week 12 ]
   Lesion volume is a measure of lesion size determined by a MRI brain scan. The cumulative volume of new GdE T1 lesions at Week 12 were analyzed from screen based on MRI brain scans at Weeks 4, 8 and 12. Anticipating an underlying negative binomial distribution with a log-link function, adjusted for treatment and presence/absence of GdE lesions on the Screening MRI. Treatment group was fitted as a categorical variable. The number of scans contributing to the cumulative volume of lesions was fitted as an offset. Estimates of the rate of cumulative volume of new GdE T1 lesions per scan at Week 12 were determined from the model. The AES dataset was used which included all evaluable on-treatment MRI scans for each par. analyzed.
6. Total Volume of All (New and Persistent) GdE Brain Lesions on T1-weighted MRI at Week 12 [ Time Frame: Week 12 ]
   Lesion volume is a measure of lesion size determined by a MRI brain scan. The cumulative volume of all (new and persistent) GdE T1 lesions at Week 12 were analyzed from screen based on MRI brain scans at Weeks 4, 8 and 12. The endpoint was analyzed using a generalized linear model assuming an underlying negative binomial distribution with a log-link function, adjusted for treatment and presence/absence of GdE lesions on the Screening MRI. Treatment group was fitted as a categorical variable. The number of scans contributing to the cumulative volume of lesions was fitted as an offset. Estimates of the rate of cumulative volume of all (new and persistent) GdE T1 lesions per scan at Week 12 were determined from the model. The AES dataset was used which included all evaluable on-treatment MRI scans for each par. analyzed.
7. Cumulative Number of New and Newly Enlarging GdE T2 Lesions at Week 12 [ Time Frame: Week 12 ]
   The cumulative number of new and newly enlarging GdE T2 lesions (NET2L) at Week 12 were analyzed from screen based on MRI brain scans at Weeks 4, 8 and 12. The endpoint was analyzed using a generalized linear model assuming an underlying negative binomial distribution with a log-link function, adjusted for treatment and presence/absence of GdE lesions on the Screening MRI. Treatment group was fitted as a categorical variable. The number of scans contributing to the cumulative number of lesions was fitted as an offset. Estimates of the rate of cumulative number of NET2L per scan at Week 12 were determined from the model. The AES dataset was used which included all evaluable on-treatment MRI scans for each par. analyzed.
8. Total Volume of New and/or Newly Enlarging T2 Lesions at Week 12 [ Time Frame: Week 12 ]
   Lesion volume is a measure of lesion size determined by a MRI brain scan. T2 lesions, are indicative of brain myelin content.The cumulative volume of new and/or newly enlarging T2 lesions at Week 12 were analyzed from screen based on MRI brain scans at Weeks 4, 8, and 12. The AES dataset was used which included all evaluable on-treatment MRI scans for each par.
9. Cumulative Number of New T1 Hypointense Lesions at Week 24 and Week 48 [ Time Frame: Week 24 and Week 48 ]
   The cumulative number of new T1 hypointense lesions at week 24 were analyzed from screen based on MRI brain scans at Weeks 4, 8, 12, 16, 20 and 24. The AES dataset was used which included all evaluable on-treatment MRI scans for each par.
10. Cumulative Volume of New T1 Hypointense Lesions at Week 24 and Week 48 [ Time Frame: Baseline, Week 24 and Week 48 ]
    Lesion volume is a measure of lesion size determined by a MRI brain scan. Baseline is defined as the participant's last available assessment prior to initiation of IP. Change from Baseline was calculated by subtracting the Baseline value from the post-Baseline value. The AES dataset was used which included all evaluable on-treatment MRI scans for each par.

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 55 Years (Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Able to provide signed, written informed consent to participate in the study
• 18-55 years of age.
• Definite diagnosis of MS according to the 2010 revisions of the McDonald diagnostic criteria for MS [Polman, 2011].
• Subjects do not have any manifestation of another type of MS other than RRMS.
• Subjects must have a relapsing-remitting course of disease with at least one of the following prior to screening:
• At least one confirmed relapse within the previous year or
• At least two confirmed relapses within the previous 2 years or
• At least one relapse in the previous 2 years, with a GdE brain lesion on an MRI scan in the past year.
• Expanded Disability Status Scale (EDSS) score of 0-5.5 (inclusive) at screening.
• Neurologically stable with no evidence of relapse for at least 30 days prior to start of Screening and during the Screening Phase (subjects who relapse during the screening Phase can be re-screened, once the relapse has resolved).
• A female subject is eligible to enter the study if she is:
• Of non-childbearing potential
• Of childbearing potential and NOT pregnant or nursing, has a negative serum pregnancy test at screening, and agrees to one of the following:
• Complete abstinence from intercourse for the period from consent into the study until 6 months after the last dose of investigational product; or,
• Consistent and correct use of one of the following acceptable methods of birth control for the period from consent into the study until 6 months after the last dose of investigational product:

Oral contraceptives (either combined or progesterone only) Injectable progesterone Levonorgestrel implants Estrogenic vaginal ring Percutaneous contraceptive patches Intrauterine device (IUD) or intrauterine system (IUS) with a documented failure rate of <1% per year Male partner sterilization (vasectomy with documentation of azoospermia) prior to the female subject's entry into the study; this male must be the sole partner for the subject Double barrier method: condom and an occlusive cap (diaphragm or cervical/vault caps) with a vaginal spermicidal agent (foam/gel/film/cream/suppository).

A female is considered "Non-childbearing potential" if she is status-post hysterectomy, status-post surgical removal of both ovaries, has current, documented tubal ligation, or is postmenopausal and >2 years without menses. Female subjects who are post-menopausal <2 years must be confirmed menopausal by Follicle Stimulating Hormone (FSH) and estradiol levels.

A female is considered "childbearing potential" if she has functional ovaries, ducts, and uterus with no impairment that would cause sterility. This includes women with oligomenorrhea (even severe), and women who are perimenopausal or who have just begun to menstruate.

• French subjects: In France, a subject will be eligible for inclusion in this study only if either affiliated to, or a beneficiary of, a social security category.

Exclusion Criteria:

• Unable to undergo MRI scans (e.g. due to pacemaker, severe claustrophobia, hypersensitivity to contrast media, or who lack adequate peripheral venous access).
• Any clinically significant brain abnormality other than MS found on MRI.
• Neurological findings consistent with Progressive Multifocal Leukoencephalopathy (PML) or confirmed PML (see Appendix 4, Section 11.4, for PML monitoring algorithm).
• Subjects whom experience a relapse during the Screening Phase. These subjects may be eligible for re-screening after consultation with GlaxoSmithKline (GSK).
• History of clinically significant Central Nervous System (CNS) trauma (e.g. traumatic brain injury, cerebral contusion, spinal cord compression) or a history or presence of myelopathy due to spinal cord compression by disk or vertebral disease.
• Prior treatment with any of the following:
• Systemic glucocorticoids or Adrenocorticotrophic hormone (ACTH) within one month prior to screening
• Receipt of a live vaccine within 6 weeks prior to screening
• Glatiramer acetate (Copaxone) or Interferon (IFN)-β (Betaferon, Betaseron, Avonex, or Rebif) within 3 months prior to screening
• Any immunomodulatory therapies, excluding glatiramer acetate or IFN-β, within 6 months prior to screening including natalizumab and fingolimod (Gilenya), immunoglobulin, or plasma exchange/plasmapheresis
• Any monoclonal antibodies at any time, other than natalizumab (Tysabri)
• Any lymphocyte-depleting therapies, including, but not limited to: cladribine, anti-Cluster of Differentiation 4 (CD4), total body irradiation, or bone marrow transplantation
• Any immunosuppressive agents, including, but not limited to: mitoxantrone, azathioprine, cyclosporine, cyclophosphamide, or tacrolimus
• Past or current history of medically significant adverse effects (including allergic reactions) from:
• Cetirizine (or equivalent)
• Paracetamol/acetaminophen
• Corticosteroids
• Known hypersensitivity to components of the investigational product.
• Past or current malignancy, except for
• Cervical carcinoma Stage 1B (cancer is present but has not spread) or less
• Non-invasive basal cell and squamous cell skin carcinoma
• Cancer diagnoses with a duration of complete response (remission) >5 years
• A history of hematologic malignancy excludes a subject from participation, regardless of response.
• Electrocardiogram (ECG) showing a clinically significant abnormality at Screening or showing an average QT interval for heart rate corrected using Bazett's Formula (QTcB) or QT interval for heart rate corrected using Fridericia's Formula (QTcF) interval >/=450 msec (>/=480 msec for subjects with a Bundle Branch Block) over 3 consecutive ECGs.
• Significant concurrent, uncontrolled medical condition including, but not limited to, cardiac, renal, hepatic, hematological, gastrointestinal, endocrine, immunodeficiency syndrome, pulmonary, cerebral, psychiatric, or neurological disease which in the opinion of the investigator could affect the subject's safety, impair the subject's reliable participation in the trial, impair the evaluation of endpoints, or necessitate the use of medication not allowed by this protocol.
• History of severe, clinically significant CNS trauma (e.g. cerebral contusion, spinal cord compression) or a history or presence of myelopathy due to spinal cord compression by disk or vertebral disease.
• Chronic or ongoing active infectious disease requiring long term systemic treatment such as, but not limited to, chronic renal infection, chronic chest infection with bronchiectasis, tuberculosis, or active hepatitis C.
• Previous serious opportunistic or atypical infections.
• Positive polymerase chain reaction (PCR) screening for John Cunningham (JC) Virus as measured by plasma John Cunningham Virus (JCV) DNA.
• Positive serology for Hepatitis B (HB) defined as a positive test for HBsAg. In addition, if negative for HBsAg but HBcAb positive (regardless of HBsAb status), a HB DNA test will be performed and if positive the subject will be excluded.
• Prior history, or suspicion, of tuberculosis (TB)
• Known history of positive serology for HIV.
• Any of the following screening laboratory values:
• White blood cells (WBC) <3.8 GI/L.
• Neutrophils <2 x 109/L.
• Platelets <1.3 x 105 GI/L.
• Circulating IgG, Immunoglobulin M (IgM), or Immunoglobulin A (IgA) levels < lower limit of normal (according to central laboratory range)
• Alanine aminotransferase (ALT) >2.0 times the upper limit of normal
• Aspartate aminotransferase (AST) >2.0 times the upper limit of normal
• Alkaline phosphatase (ALP) >1.5 times the upper limit of normal
• Bilirubin >1.5 times the upper limit of normal
• CD4 count <500 cells/mm3.
• CD19+ B-lymphocyte counts < lower limit of normal (according to central laboratory range)
• Creatinine clearance <60 mL/minute (by Cockcroft and Gault).
• Subjects known or suspected of not being able to comply with a trial protocol (e.g. due to alcoholism, drug dependency or psychological disorder).
• A documented history of attempted suicide over the 6 months prior to the screening visit, presents with suicidal ideation of type 4 or 5 on the C-Suicide Severity Rating Scale (SSRS) at the Screening visit, OR if in the investigator's judgment, the subject is at risk for a suicide attempt.
• Use of an investigational drug or other experimental therapy for a condition other than MS within 4 weeks, 5 pharmacokinetic half lives or duration of biological effect (whichever is longer) prior to screening. Any prior use of an investigational drug or other experimental therapy for MS at any time should be discussed with the GSK Medical Monitor.
• Current participation in any other interventional clinical trial. Participation in a non-interventional trial requires approval of the protocol by the GSK Medical Monitor
• French subjects: the French subject has participated in any study using an investigational drug during the previous 30 days

Contacts and Locations

Locations

United States, Alabama

GSK Investigational Site

Cullman, Alabama, United States, 35058

United States, California

GSK Investigational Site

Fullerton, California, United States, 92835

United States, Connecticut

GSK Investigational Site

Fairfield, Connecticut, United States, 06824

United States, Florida

GSK Investigational Site

Miami, Florida, United States, 33136

GSK Investigational Site

Sunrise, Florida, United States, 33351

GSK Investigational Site

Tampa, Florida, United States, 33612

GSK Investigational Site

West Palm Beach, Florida, United States, 33407

United States, Georgia

GSK Investigational Site

Atlanta, Georgia, United States, 30327

United States, Illinois

GSK Investigational Site

Northbrook, Illinois, United States, 60062

United States, Indiana

GSK Investigational Site

Fort Wayne, Indiana, United States, 46805

United States, Michigan

GSK Investigational Site

Grand Rapids, Michigan, United States, 49503

United States, Oklahoma

GSK Investigational Site

Oklahoma City, Oklahoma, United States, 73104

United States, Pennsylvania

GSK Investigational Site

Philadelphia, Pennsylvania, United States, 19107

United States, Tennessee

GSK Investigational Site

Nashville, Tennessee, United States, 37204

United States, Texas

GSK Investigational Site

Round Rock, Texas, United States, 78681

United States, Washington

GSK Investigational Site

Seattle, Washington, United States, 98122

Bulgaria

GSK Investigational Site

Sofia, Bulgaria, 1000

GSK Investigational Site

Sofia, Bulgaria, 1113

GSK Investigational Site

Sofia, Bulgaria, 1309

GSK Investigational Site

Sofia, Bulgaria, 1431

Canada, Alberta

GSK Investigational Site

Edmonton, Alberta, Canada, T6G 1Z1

Canada, Quebec

GSK Investigational Site

Montreal, Quebec, Canada, H3A 2B4

Czechia

GSK Investigational Site

Brno, Czechia, 625 00

GSK Investigational Site

Brno, Czechia, 656 91

GSK Investigational Site

Jihlava, Czechia, 586 33

GSK Investigational Site

Olomouc, Czechia, 775 20

GSK Investigational Site

Teplice, Czechia, 415 29

Denmark

GSK Investigational Site

Koebenhavn Ø, Denmark, 2100

Germany

GSK Investigational Site

Alzenau, Bayern, Germany, 63755

GSK Investigational Site

Achim, Niedersachsen, Germany, 28832

GSK Investigational Site

Hannover, Niedersachsen, Germany, 30625

GSK Investigational Site

Bochum, Nordrhein-Westfalen, Germany, 44791

GSK Investigational Site

Koeln, Nordrhein-Westfalen, Germany, 50935

GSK Investigational Site

Leipzig, Sachsen, Germany, 04103

GSK Investigational Site

Berlin, Germany, 10961

GSK Investigational Site

Berlin, Germany, 12163

GSK Investigational Site

Hamburg, Germany, 22087

Italy

GSK Investigational Site

Modena, Emilia-Romagna, Italy, 41126

GSK Investigational Site

Verona, Veneto, Italy, 37134

Netherlands

GSK Investigational Site

Sittard-geleen, Netherlands, 6162 BG

GSK Investigational Site

Venray, Netherlands, 5801 CE

Norway

GSK Investigational Site

Hamar, Norway, 2317

Russian Federation

GSK Investigational Site

Kazan, Russian Federation, 420021

GSK Investigational Site

Moscow, Russian Federation, 107150

GSK Investigational Site

Moscow, Russian Federation, 119049

GSK Investigational Site

Moscow, Russian Federation, 127018

GSK Investigational Site

N. Novgorod, Russian Federation, 603126

GSK Investigational Site

Smolensk, Russian Federation, 214018

GSK Investigational Site

St. Petersburg, Russian Federation, 197022

GSK Investigational Site

St.Petersburg, Russian Federation, 194291

Spain

GSK Investigational Site

Baracaldo/Vizcaya, Spain, 48903

GSK Investigational Site

Barcelona, Spain, 08035

GSK Investigational Site

Barcelona, Spain, 08907

GSK Investigational Site

Castellón, Spain, 12004

GSK Investigational Site

Córdoba, Spain, 14001

GSK Investigational Site

Girona, Spain, 17007

GSK Investigational Site

Madrid, Spain, 28034

GSK Investigational Site

Madrid, Spain, 28040

GSK Investigational Site

Madrid, Spain, 28046

GSK Investigational Site

Malaga, Spain, 29010

GSK Investigational Site

Sevilla, Spain, 41071

Sponsors and Collaborators

GlaxoSmithKline

Investigators

• Study Director: GSK Clinical Trials; GlaxoSmithKline

More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Bar-Or A, Grove RA, Austin DJ, Tolson JM, VanMeter SA, Lewis EW, Derosier FJ, Lopez MC, Kavanagh ST, Miller AE, Sorensen PS. Subcutaneous ofatumumab in patients with relapsing-remitting multiple sclerosis: The MIRROR study. Neurology. 2018 May 15;90(20):e1805-e1814. doi: 10.1212/WNL.0000000000005516. Epub 2018 Apr 25. Erratum In: Neurology. 2018 Sep 11;91(11):538.

• Responsible Party: GlaxoSmithKline
• ClinicalTrials.gov Identifier: NCT01457924
• Other Study ID Numbers: 112831
• First Posted: October 24, 2011
• Results First Posted: March 1, 2018
• Last Update Posted: June 6, 2018
• Last Verified: May 2018

Keywords provided by GlaxoSmithKline:

Relapsing Remitting Multiple Sclerosis; Ofatumumab

Additional relevant MeSH terms:

Ofatumumab; Multiple Sclerosis; Multiple Sclerosis, Relapsing-Remitting; Sclerosis; Pathologic Processes; Demyelinating Autoimmune Diseases, CNS; Autoimmune Diseases of the Nervous System; Nervous System Diseases; Demyelinating Diseases; Autoimmune Diseases; Immune System Diseases; Antibodies, Monoclonal; Antineoplastic Agents; Immunologic Factors; Physiological Effects of Drugs