ATX-MS-1467 in Multiple Sclerosis

Merck KGaA (EMD Serono)

Status and phase

Completed

Phase 2

Conditions

Multiple Sclerosis

Treatments

Drug: ATX-MS-1467

Study type

Interventional

Funder types

Industry

Identifiers

NCT01973491

2013-002916-28 (EudraCT Number)

200166-001

Details and patient eligibility

About

This is a multi-center, open-label, single arm, baseline-controlled Phase 2a trial to evaluate the clinical and biological effects of ATX-MS-1467 in subjects with relapsing multiple sclerosis (MS) and to assess the maintenance of any such effects.

Enrollment

37 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female out-patients aged 18 to 65 years of age inclusive at the time of informed consent
Willing and able to provide written informed consent and to comply with the requirements of the protocol assessments/procedures
Relapsing MS (relapsing-remitting multiple sclerosis [RRMS], secondary progressive multiple sclerosis [SPMS], as defined by the revised McDonald criteria [2010]) (11)
Clinical evidence of recent MS activity and radiological activity on gadolinium (Gd)-enhanced magnetic resonance imaging (MRI) defined as defined in the protocol
Expanded disability status scale (EDSS) score 0-5.5
Human leukocyte antigen-beta chain (HLA-DRB)1*15 positive
Neurological stability in the 30 days prior to Visit 5 (Study Day 1)
Prior vaccination against tuberculosis (TB)
If female, unless post-menopausal (for at least 2 years) or surgically sterilized, must be willing to use two highly effective methods of contraception throughout the entire duration of the trial and for 90 days following the last dose of ATX-MS-1467
If male, must be willing to use two highly effective methods of contraception throughout the entire duration of the trial and for 90 days following the last dose of ATX-MS-1467

Exclusion criteria

Primary progressive MS
Inability to comply with MRI scanning, including contra-indications to MRI such as known allergy to gadolinium contrast dyes, claustrophobia, presence of a pacemaker, cochlear implants, ferromagnetic devices or clips, intracranial vascular clips, insulin pumps, nerve stimulators
Previous treatment with beta-interferon, plasma exchange, intravenous gamma globulin within the 8 weeks prior to study Day 1 (Visit 5), steroids (administered via the oral and/or parenteral routes) or adrenocorticotropic hormone within the 30 days prior to the Visit 2 MRI scan, glatiramer acetate, cytotoxic agents
Prior exposure to dimethyl fumurate (BG-12) or dirucotide, any disease-related T cell vaccine or peptide-tolerizing agent for the treatment of MS, including ATX-MS-1467
Use of any investigational drug or experimental procedure for MS (including cytokine or anticytokine therapy) within the 30 days prior to screening (Visit 1)
Inadequate liver function as defined in the protocol.
Lymphocyte count less than (<)500 per micro liter (/mcL) or neutrophil count < 1500 mcL at screening or at any of the pre-treatment visits (Visits 2-4)
Major medical illness as defined in the protocol
Known history of active or chronic infectious disease or any disease which compromises immune function
Any renal condition that would preclude the administration of gadolinium
History of malignancy, including both solid tumor and hematological malignancies, but excluding basal cell and in situ squamous cell carcinomas of the skin that have been excised and resolved, in situ cervical cancer or prostatic cancer with normal prostatic specific antigen
Clinical evidence of severe uncontrolled depression, active suicidal ideation or suicide attempt
Any other significant medical or psychiatric conditions that, in the opinion of the Investigator, would preclude participation in the trial or impair the ability to give informed consent
Major surgery in the 4 weeks prior to screening (Visit 1)
Known hypersensitivity to the trial medication or diluents
Participation in another clinical trial within the 30 days prior to screening (Visit 1)
Pregnancy, lactation or a positive pregnancy test during screening (urine dipstick) or at Visit 4 (serum beta-human chorionic gonadotrophin [beta-hCG]), or intention to become pregnant or to breast-feed during the course of the trial
Legal incapacity or limited legal capacity