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Completed

NCT Number: NCT01097668

ATX-MS-1467 in Patients With Relapsing Forms of Multiple Sclerosis

Phase 1 study to assess the safety and biological activity of ATX-MS-1467 in patients with relapsing forms of multiple sclerosis. This will be an open label upward dose titration involving injections on 9 occasions, each two weeks apart. After dosing is complete there will be a 22 week follow up period. Blood samples will be drawn throughout the study to monitor safety and the body's response to the injections and MRI scans will be performed on several occasions to follow the course of the multiple sclerosis during the trial.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Municipal Healthcare Institution "City Clinical Hospital #3", Department of neurology, Chelyabinsk, Russia

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.
  • HLA DRB1*15 positive.
  • 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.
  • Disease duration equal to or less than 10 years (from the first clinical event).
  • At least one documented relapse in the previous 12 months or two relapses within the previous 24 months prior to screening.
  • Must be in a clinically stable or improving neurological state during the 28 days preceding Screening.
  • EDSS score < 5.5.

Exclusion criteria

  • 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

Treatment and study plan

ATX-MS-1467

Biological

Disease specific immune modulating treatment for multiple sclerosis

Primary outcomes

  1. Safety and Tolerability

    Time frame: 48 weeks

    Occurrence of treatment emergent Adverse Events (AE), Serious Adverse Events, and laboratory abnormalities up to week 48 compared to baseline.

Secondary outcomes

  1. The Effect of ATX-MS-1467 on Brain Magnetic Resonance Imaging (MRI).

    Time frame: 16 and 20 weeks

    Number of new or persisting Gadolinium-enhancing lesions at week 16 and 20 when compared to baseline.

Sponsors and collaborators

Lead sponsor

Apitope Technology (Bristol) Ltd.

Industry

Collaborators

  • Aptiv Solutions
  • ClinStar, LLC

Registry information

Official study title

SAFETY AND PROOF OF PRINCIPLE STUDY OF ATX-MS-1467 IN PATIENTS WITH RELAPSING MULTIPLE SCLEROSIS: OPEN LABEL UPWARD TITRATION OVER FIVE DOSE LEVELS AND USING TWO ROUTES OF ADMINISTRATION (INTRADERMAL AND SUBCUTANEOUS).

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Apr 2, 2010
Registry last updated
Feb 16, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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