Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Apitope Technology (Bristol) Ltd.
With
Aptiv Solutions
ClinStar, LLC
Age
18–55
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
1\. Patients who have definite relapsing multiple sclerosis disease as defined by the McDonald criteria (McDonald et al., 2001 and 2005) and as assessed by a neurologist.
2\. HLA DRB1\*15 positive.
3\. High baseline levels of T-cell proliferation in response to myelin basic protein, defined as \>1000 cpm with a \>3 stimulation index compared to background.
4\. Disease duration equal to or less than 10 years (from the first clinical event).
5\. At least one documented relapse in the previous 12 months or two relapses within the previous 24 months prior to screening.
6\. Must be in a clinically stable or improving neurological state during the 28 days preceding Screening.
7\. EDSS score \< 5.5.
You may not be if
1\. Subjects treated with β-interferon, plasma exchange, intravenous gamma globulin within the 3 months prior to Study Day 1 2. Subjects treated with glatiramer acetate at any time in the past 3. Subjects who have been treated with parenteral steroids or adrenocorticotropic hormone within 3 months days prior to Study Day 1 4. Prior treatment with: cytotoxic agents (including but not limited to cladribine, mitoxantrone, cyclophosphamide, azathioprine, methotrexate), fingolimod, laquinimod, teriflunomide, total lymphoid irradiation, stem cell or bone marrow transplantation, or monoclonal antibody therapy (including natalizumab, daclizumab, alemtuzumab) 5. Prior use of disease related T-cell vaccine or peptide-tolerising agent to treat MS 6. Use of any investigational drug or experimental procedure within 6 months prior to Study Day 1 including cytokine or anti-cytokine therapy
Clareo Health | ATX-MS-1467 in Patients With Relapsing Forms of Multiple Sclerosis
