Safety and Efficacy Study of MIS416 to Treat Secondary Progressive Mul
A Phase 2B Randomised, Double-Blind, Placebo-Controlled Trial of the Efficacy and Safety of MIS416 in the Treatment of Subjects With Secondary Progressive Multiple Sclerosis
What it found
We found no results in the registry or in papers.
This trial finished 9 years ago. We found no results in the registry or in any paper that cites it.
What was tested
Treatment tested
- MIS416
Placebo
- Saline
What it measured
Main measures
Change from baseline of neuromuscular function at 12 months
Baseline, 3, 6, 9 and 12 months
Disability progressionVisionThinking and memoryWalking and mobilityArm and hand functionPhysical functionProportion of Participants with Serious and Non-Serious Adverse Events
Up to 12 months
MRI lesionsSafety
Other measures (5)
Change from baseline of disability and health status at 12 months
Baseline, 3, 6, 9, and 12 months
Disability progressionFatiguePainQuality of life (reported by participants)Change from baseline of neurodegeneration by assessing changes in Magnetic Resonance Imaging (MRI) markers at 12 months
Baseline, 3, and 12 months
MRI lesionsBrain volume lossMyelin repairChange from baseline of activity of immune biomarkers in serum
Up to 1 year
Blood or spinal fluid markersImmune responseChange from baseline of activity of immune biomarkers in cerebrospinal fluid (CSF)
Up to 12 months
Blood or spinal fluid markersImmune responseChange from baseline in Peripheral Blood Mononuclear Cell (PBMC) immune biomarkers
Up to 12 months
Blood or spinal fluid markersImmune response
Who could take part
Progressive MS · 18 to 70 · EDSS 3.0 to 6.5
Show the full criteria
Inclusion criteria
1. A historical or current cranial MRI scan demonstrating T2-hyperintense lesions consistent with MS. 2. Has SPMS as determined by the 2010 Update to the McDonald Criteria 3. An Expanded Disability Status Scale (EDSS) of 3.0 to 6.5 at Screening. 4. Has SPMS which, in the judgment of the investigator, has been clinically active and functionally progressive within the 2 years prior to Screening 5. The absence of MS relapse for at least two years prior to Baseline. 6. Neurologically stable for at least four weeks prior to Screening. 7. Has the following laboratory values within three days prior to initiation of Investigational Product: * Absolute neutrophil count (ANC) >= 1 x 109/L; * Platelet count >= 100 x 109/L; * Serum creatinine =\< 1.5 mg/dL; * Aspartate aminotransferase (AST) =\<2 × upper limit of normal; * Alanine aminotransferase (ALT) =\< 2 × upper limit of normal. 8. Provided written informed consent to participate.
Exclusion criteria
1. Has primary Progressive MS (PPMS), Relapsing Remitting (RRMS), or progressive relapsing MS as determined by the 2010 update to the McDonald Criteria. 2. Has not completed the discontinuation period for approved and/or investigational multiple sclerosis disease modifying therapies prior to screening. 3. Has had any other immunomodulatory drug therapy or immunosuppressive therapy within four weeks prior to Screening, or systemic corticosteroids within the eight weeks prior to Screening. 4. Any previous exposure to investigational MS therapeutic vaccines. 5. Any use of cell-depleting monoclonal antibodies including, but not limited to, Rituximab, or Ocrelizumab. 6. A diagnosis or history of collagen vascular disease (including Sjögren's syndrome and systemic lupus erythematosus), anticardiolipin antibody syndrome, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, sarcoidosis, vasculitis, Behcet's syndrome and/or Lyme disease. 7. Contraindication to MRI (e.g., pacemaker or other contraindicated implanted metal device, allergy to gadolinium, or unmanageable claustrophobia). 8. A history of alcohol or drug abuse (including cannabinoid use) within two years prior to Screening. 9. Has had major surgery or radiation therapy within four weeks prior to Screening. 10. Has an active infection requiring antibiotics within two weeks prior to Screening. 11. Has had active malignancy within two years of Screening, with the exception of basal cell carcinoma and squamous cell carcinoma of the skin. 12. Uncontrolled congestive heart failure, myocardial infarction, cerebrovascular accident, coronary/peripheral artery bypass graft surgery, or transient ischemic attack within twelve weeks prior to Screening. 13. Has angina, other symptomatic coronary artery disease, or known cardiomyopathy. 14. Has symptomatic cardiac dysrhythmias requiring treatment, or persistent prolongation of the QTcF (Fredericia) interval to > 450 msec for males or > 470 msec for females.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
The purpose of this study is to determine whether MIS416 administered once weekly over 12 months is safe, tolerable, and improves a range of signs and symptoms associated with secondary progressive multiple sclerosis.
Papers
Loading reviews and guidelines…
History
Started
Oct 2014
Main results due
May 2017
Finished
Jun 2017