Informations générales (source: ClinicalTrials.gov)
A Phase 2 Trial Assessing Ifenprodil as a ReMyelinating repurpOsed Drug in Multiple Sclerosis
Interventional
Phase 2
Assistance Publique - Hôpitaux de Paris (Voir sur ClinicalTrials)
mars 2024
juin 2027
03 décembre 2025
Multiple sclerosis (MS) is the most frequently acquired demyelinating disease and the
first cause of non-traumatic chronic disability in young adults. Major progress has been
achieved in the treatment of MS through the development of therapies targeting the
adaptative immune system, which drastically reduce the relapse rate, with various
efficiency and safety profiles (Ontaneda, 2015). However, these drugs generally fail to
prevent disability worsening along the disease course, and we are now assisting to a
shift in therapeutic objectives from the development of new immune drugs towards the
identification of therapeutic strategies that could prevent neurodegeneration by
promoting myelin regeneration (Stangel, 2017; Stankoff, 2016), in order to prevent
neurological disability in MS (Irvine and Blakemore, 2008; Patrikios, 2006; Duncan I,
2017, Bodini, 2016).
Among the first candidate compounds developed to promote remyelination was the anti
Lingo1 antibody, which enhance remyelination (Mi, 2009). Medium and large throughput
screening of drug libraries subsequently identified several chemical classes of compounds
with strong promyelinating properties, such as the antifongic drug miconazole (Najm,
2015) or the muscarinic antagonist clemastine (Wei, 2014). A recent innovative trial has
investigated the effect of clemastine, compared to placebo, in a small sample of subjects
(25 patients per group) and showed that clemastine could significantly improve the optic
nerve conduction speed which reflecting myelin integrity and functionality (Green, 2017).
Our preclinical research has allowed us to identify ifenprodil as a powerful drug to
promote myelin repair in vitro and in vivo across species. In parallel our team recently
pioneered and optimized a PET imaging approach for quantifying remyelination in the whole
brain, that allowed to enhance the sensitivity to detect the myelin repair process, and
showed that patients are characterized by heterogeneous profiles of spontaneous
remyelination profiles that are closely linked to disability accrual (Bodini, 2016).
Etablissements
| Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| AP-HP Assistance publique - Hôpitaux de Paris | 13/12/2025 07:26:10 | Contacter | |||
| AP-HP - Hôpital Saint Antoine | |||||
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| Groupe Hospitalier Pitié Salpêtrière - APHP - 75013 - Paris - France | Bruno STANKOFF, MD | Contact (sur clinicalTrials) | |||
| Hôpital Neurologique Pierre WERTHEIMER - HCL - 69677 - Bron - France | Françoise DURAND DUBIEF, MD | Contact (sur clinicalTrials) | |||
Critères
Tous
Inclusion Criteria:
- Patients:
1. Signed informed consent form at pre-inclusion visit
2. Age between 18 years and 55 years, inclusive, at time of pre-inclusion visit.
3. Patient with a RR form of MS according McDonald criteria 2017 at pre-inclusion visit
4. Able to comply with the study protocol and to understand the purpose and risks of
the study, in the investigator's judgment
5. Social security registration (AME excluded) at time of pre-inclusion visit
6. At least one eye with a P100 latency > 118ms on visual evoked potential at baseline
(defining the qualifying eye) at time of pre-inclusion visit
7. Retinal nerve fibre layer thickness on spectral-domain optical coherence tomography
[OCT] > 70 μm in the VEP qualifying eye (to increase the likelihood that the number
of surviving axons is sufficient to provide the substrate for remyelination to
occur) at time of pre-inclusion visit
8. Patient under disease modifying therapy (first or second line approved immune active
therapy) or patient without any DMT at time of pre-inclusion visit
9. EDSS score ≤ 6 at time of pre-inclusion visit
10. For women of childbearing potential : Efficient contraception include oral
contraception, intrauterine devices hormonal device, intrauterine hormone-releasing
system, sterilization method and other forms of contraception with failure rate <1%)
- Healthy Volunteers
1. Signed informed consent form 2. Age between 18 years and 55 years, inclusive 3. All
female subjects of childbearing potential must practice effective contraception
include oral contraception, intrauterine devices hormonal device, intrauterine
hormone-releasing system, sterilization method and other forms of contraception with
failure rate <1%) 4. Able to comply with the study protocol, in the investigator's
judgment 5. Social security registration (AME excluded)
- Patients:
1. Signed informed consent form at pre-inclusion visit
2. Age between 18 years and 55 years, inclusive, at time of pre-inclusion visit.
3. Patient with a RR form of MS according McDonald criteria 2017 at pre-inclusion visit
4. Able to comply with the study protocol and to understand the purpose and risks of
the study, in the investigator's judgment
5. Social security registration (AME excluded) at time of pre-inclusion visit
6. At least one eye with a P100 latency > 118ms on visual evoked potential at baseline
(defining the qualifying eye) at time of pre-inclusion visit
7. Retinal nerve fibre layer thickness on spectral-domain optical coherence tomography
[OCT] > 70 μm in the VEP qualifying eye (to increase the likelihood that the number
of surviving axons is sufficient to provide the substrate for remyelination to
occur) at time of pre-inclusion visit
8. Patient under disease modifying therapy (first or second line approved immune active
therapy) or patient without any DMT at time of pre-inclusion visit
9. EDSS score ≤ 6 at time of pre-inclusion visit
10. For women of childbearing potential : Efficient contraception include oral
contraception, intrauterine devices hormonal device, intrauterine hormone-releasing
system, sterilization method and other forms of contraception with failure rate <1%)
- Healthy Volunteers
1. Signed informed consent form 2. Age between 18 years and 55 years, inclusive 3. All
female subjects of childbearing potential must practice effective contraception
include oral contraception, intrauterine devices hormonal device, intrauterine
hormone-releasing system, sterilization method and other forms of contraception with
failure rate <1%) 4. Able to comply with the study protocol, in the investigator's
judgment 5. Social security registration (AME excluded)
Patients
1. Patient with an acute NORB in the last 6 months prior to pre-inclusion visit
2. Patient with a clinical relapse other than NORB in the last 6 months prior to
pre-inclusion visit
3. Patients having received methylprednisolone infusion in the last 4 weeks prior to
pre-inclusion visit
4. Contraindications to investigational medicinal products (ifenprodil/placebo) and to
auxiliary medicinal products (gadolinium, [18F]-florbetaben)
5. Inability to complete an MRI (contraindications for MRI include but are not
restricted to weight ≥ 140 kg, pacemaker, cochlear implants, presence of foreign
substances in the eye, intracranial vascular clips, surgery within 6 weeks of entry
into the study, coronary stent implanted within 8 weeks prior to the time of the
intended MRI, contraindication to gadoteric acid etc.).
6. PET imaging performed in the past 12 months as part of clinical research
7. History or incidental discovery of significant cardiac conduction block
8. Orthostatic hypotension Syndrome define as a drop of > 20 mmHg in systolic, and/or >
10 mmHg in diastolic between lying down and immediate standing
9. Known long QT syndrome or long QT syndrome (the limit is defined at 450 ms on
corrected QT) highlighted during the pre-inclusion visit
10. Any uncontrolled general (cancer, infectious, hematologic, hepatic, immunologic,
endocrinologic, neurologic, dermatologic, psychiatric, allergic, renal, or
cardiovascular) disease.
11. Creatinine clearance < 60 ml/min at pre-inclusion visit
12. ASAT, ALAT of alkaline phosphatase > 3-fold the upper limit normal at pre-inclusion
visit
13. Know Galactosemia, glucose malabsorption or lactase deficiency
14. Known of lack of peripheral venous access or lack of peripheral venous access
highlighted during the pre-inclusion visit
15. Thrombocytopenia with platelets < 100 000/mm3
16. Pregnancy and/or lactating women
17. Legal protection (curatorship or tutorship)
18. Deprive of freedom or under security measure
19. Participation in another interventional trial evaluating a health product or any
randomized trial or being in the exclusion period at the end of a previous study
20. Refusal to be informed in case of clinically significant incidental discovery after
MRI
21. Patient treated for hypertension with the following drugs blocking the
alpha-adrenergic system either in periphery (prazosine, urapidil, moxisylyte,
labetalol) or centrally (clonidine, monoxidine, methyldopa)
Healthy Volunteers
1. Inability to complete an MRI (contraindications for MRI include but are not
restricted to weight ≥ 140 kg, pacemaker, cochlear implants, presence of foreign
substances in the eye, intracranial vascular clips, surgery within 6 weeks of entry
into the study, coronary stent implanted within 8 weeks prior to the time of the
intended MRI, etc).
2. Impossibility to complete a PET scan: pregnancy, nuclear medicine irradiation for
clinical research in the year preceding baseline visit.
3. Contraindication to auxiliary medicinal products ([18F]-florbetaben)
4. Known presence of any neurological disorders
5. Pregnancy and/or lactation
6. Lack of peripheral venous access
7. Terminal renal insufficiency (Creatinin clearance < 60 ml/min)
8. Legal protection (curatorship or tutorship)
9. Deprive of freedom or under security measure
10. Participation in another interventional trial evaluating a health product or any
randomized trial or being in the exclusion period at the end of a previous study
11. Refusal to be informed in case of clinically significant incidental discovery after
MRI