E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
|
MedDRA Classification |
E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
To demonstrate the effect of teriflunomide (7and 14 mg/d) compared to placebo for reducing conversion of patients presenting their first clinical episode consistent with MS to clinically definite MS. |
|
E.2.2 | Secondary objectives of the trial |
To demonstrate effect of teriflunomide (7and 14 mg/d) compared to placebo for: reducing conversion to definite MS by the demonstration of dissemination of MRI lesions in time, reducing annualized relapse rate, reducing MRI parameters reflecting disease progression/burden, reducing accumulation of disability as measured by EDSS, reducing patient-reported fatigue.
To evaluate safety and tolerability of teriflunomide. |
|
E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
1.Patients with a first acute or subacute, well-defined neurological event consistent with demyelination (i.e. optic neuritis confirmed by an ophthalmologist, spinal cord syndrome, brainstem/cerebellar syndromes)
2. Onset of MS symptoms occurring within 60 days of randomization
3. A screening MRI scan (performed at Visit 1) with 2 or more T2 lesions at least 3 mm in diameter that are characteristic of MS (i.e. at least one lesion is periventricular in location or ovoid in shape) |
|
E.4 | Principal exclusion criteria |
1. Unable to obtain written informed consent
2. Mental condition rendering the patient unable to understand the nature, scope, and possible consequences of the study
3. Patient unlikely to comply with protocol, e.g., uncooperative attitude, inability to return for follow-up visits, and known unlikelihood of completing the study
4. Age < 18 years or >55 years
5. Contraindication for MRI, e.g., presence of pacemaker, metallic implants in high-risk areas
6. Clinically relevant cardiovascular, hepatic, neurological, endocrine, or other major systemic disease making implementation of the protocol or interpretation of the study results difficult or that would put the patient at risk by participating in the study
7. Patients with a congenital or acquired severe immunodeficiency, a history of cancer , lymphoproliferative disease, or any patient who has received lymphoid irradiation
8. Known history of active tuberculosis not adequately treated
9. Persistent significant or severe infection
10. History of drug or alcohol abuse
11. Patient is the investigator or any sub-investigator, research assistant, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the protocol
12. Patients must not have used Adrenocorticotrophic hormone (ACTH) or systemic corticosteroids for 2 weeks prior to randomization
13. Prior use within 4 weeks before randomization or concomitant use of phenytoin, warfarin,tolbutamide, or cholestyramine
14. St. John's Wort products containing hyperforin in an unknown percentage or greater than 1% of the extract.
15. Prior or concomitant use of cladribine, mitoxantrone, or other immunosuppressant agents such as azathioprine, cyclophosphamide, cyclosporin, methotrexate or mycophenolate
16. Prior or concomitant use of interferons, cytokine therapy, glatiramer acetate or intravenous immunoglobulins 17. Prior or concomitant use of natalizumab (Tysabri®)
18. Prior treatment with teriflunomide, and prior or concomitant use of leflunomide (ARAVA®) or hypersensitivity to any of the other ingredients or excipients of the investigational product.
19. Prior use of any investigational drug in the preceding 6 months
20. Pregnant or breast-feeding women
21. Women of childbearing potential not protected by effective contraceptive method of birth control and/or who are unwilling or unable to be tested for pregnancy.
22. Patients wishing to parent children during the course of the trial.
23. Patients with significantly impaired bone marrow function or significant anemia, leukopenia, or thrombocytopenia • Hematocrit <24% and/or • Absolute white blood cell count <4,000 cells/ mm3 (μL) and/or • Platelet count <150,000 cells/ mm3 (μL) and/or • Absolute neutrophil ≤ 1,500 cells/ mm3 (μL)
24. Human immunodeficiency virus (HIV) positive patient requiring concomitant use of antiretroviral nucleoside analogs (i.e. AZT, ddI, ddC, d4T, 3TC, combivir and abacavir)
25. Persisting elevations (confirmed by retest) of serum amylase or lipase greater than 2-fold the upper limit of normal
26. Known history of chronic pancreatic disease or pancreatitis
27. Liver function impairment or persisting elevations (confirmed by retest) of serum glutamicpyruvic transaminase (SGPT/ALT), serum glutamic oxaloacetic transaminase (SGOT/AST),or direct bilirubin greater than 1.5-fold the upper limit of normal
28. Known history of active hepatitis.
27. Hypoproteinemia (e.g., in case of severe liver disease or nephrotic syndrome) with serumalbumin <3.0 g/dL
28. Moderate to severe impairment of renal function, as shown by serum creatinine >133 μmol/L |
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E.5 End points |
E.5.1 | Primary end point(s) |
The primary endpoint is efficacy (conversion to clinically definite MS). |
|
E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | Information not present in EudraCT |
E.6.2 | Prophylaxis | Information not present in EudraCT |
E.6.3 | Therapy | Information not present in EudraCT |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | Yes |
E.6.7 | Pharmacodynamic | Information not present in EudraCT |
E.6.8 | Bioequivalence | Information not present in EudraCT |
E.6.9 | Dose response | Information not present in EudraCT |
E.6.10 | Pharmacogenetic | Information not present in EudraCT |
E.6.11 | Pharmacogenomic | Information not present in EudraCT |
E.6.12 | Pharmacoeconomic | Information not present in EudraCT |
E.6.13 | Others | Information not present in EudraCT |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | Information not present in EudraCT |
E.7.1.2 | Bioequivalence study | Information not present in EudraCT |
E.7.1.3 | Other | Information not present in EudraCT |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | Yes |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 9 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 73 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
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E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
| |
E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 3 |
E.8.9.1 | In the Member State concerned months | 8 |
E.8.9.1 | In the Member State concerned days | |
E.8.9.2 | In all countries concerned by the trial years | 3 |
E.8.9.2 | In all countries concerned by the trial months | 8 |