| NCT ID | Title | Phase | Status | Enrollment | Velocity | Design | Start | Completion | Last Updated | Sites | Countries |
|---|---|---|---|---|---|---|---|---|---|---|---|
| NCT06372145 | A Study to Investigate Long-term Safety and Tolerability of Tolebrutinib in Participants With Multiple Sclerosis. | PHASE3 | ACTIVE NOT_RECRUITING | 2,500 | — | — | Apr 16, 2024 | Apr 30, 2029 | Feb 13, 2026 | 352 | United States, Argentina +45 |
| NCT04410978 | Relapsing Forms of Multiple Sclerosis (RMS) Study of Bruton's Tyrosine Kinase (BTK) Inhibitor Tolebrutinib (SAR442168) (GEMINI 1) | PHASE3 | COMPLETED | 974 | — | — | Jun 30, 2020 | Jul 15, 2024 | Jul 2, 2025 | 179 | United States, Austria +22 |
| NCT04410991 | Relapsing Forms of Multiple Sclerosis (RMS) Study of Bruton's Tyrosine Kinase (BTK) Inhibitor Tolebrutinib (SAR442168) (GEMINI 2) | PHASE3 | COMPLETED | 899 | — | — | Jun 11, 2020 | Jul 16, 2024 | Jul 2, 2025 | 186 | United States, Argentina +26 |
| NCT03996291 | Long Term Safety and Efficacy Study of Tolebrutinib (SAR442168) in Participants With Relapsing Multiple Sclerosis | PHASE2 | COMPLETED | 125 | — | — | Sep 23, 2019 | Nov 26, 2024 | Oct 23, 2025 | 37 | United States, Canada +7 |
Potentially clinically significant abnormalities (PCSAs) determined by laboratory tests, electrocardiogram (ECG), or vital signs and safety findings on MRI during the study period.
Multiple sclerosis (MS) relapse was defined as a monophasic, acute or subacute onset of new neurological symptoms or worsening of previous neurological symptoms with an objective change on neurological examination. Symptoms were attributable to MS, lasted for \>=24 hours with or without recovery, present at normal body temperature, and preceded by \>=30 days of clinical stability.
An AE was any untoward medical occurrence in a participant or clinical study participant, temporally associated with the use of study drug, whether or not considered related to the study drug. An SAE was any untoward medical occurrence that at any dose: resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent disability/incapacity, was a congenital anomaly/birth defect or was an important medical event. TEAEs were defined as AEs that developed, worsened or became serious during the respective on-treatment periods.
| Arm | Type | Description |
|---|---|---|
| Tolebrutinib | EXPERIMENTAL | * Participants will receive OL tolebrunitib 60 mg once daily. * RMS participants who are not eligible for OL tolebrutinib per Health Authority and/or ethics committee decisions on the study conduct (ie, partial hold on initiation of tolebrutinib) will continue their parent study treatment assignment as per their randomization from the parent study. |
| Teriflunomide | ACTIVE_COMPARATOR | * participants will receive teriflunomide 14 mg daily * RMS participants who are not eligible for OL tolebrutinib per Health Authority and/or ethics committee decisions on the study conduct (ie, partial hold on initiation of tolebrutinib) will continue their parent study treatment assignment (either tolebrutinib or teriflunomide) as per their randomization from the parent study. If unblinded to teriflunomide parent study treatment assignment, these RMS participants will continue teriflunomide in the LTS17043 study. |
| SAR442168 | EXPERIMENTAL | 60 mg oral SAR442168 + placebo to match the teriflunomide tablet once daily |
| Name | Type | Description |
|---|---|---|
| Tolebrutinib | DRUG | Pharmaceutical form:Tablet-Route of administration:oral |
| Placebo | DRUG | Pharmaceutical form:Tablet-Route of administration:oral |
| Teriflunomide | DRUG | Pharmaceutical form:Tablet-Route of administration:oral |
| Placebo to match Tolebrutinib | DRUG | Pharmaceutical form: Tablet Route of administration: Oral |
| Placebo to match Teriflunomide | DRUG | Pharmaceutical form: Tablet Route of administration: Oral |
| Teriflunomide HMR1726 | DRUG | Pharmaceutical form: Tablet Route of administration: Oral |
Inclusion Criteria: \- Participants with RMS, PPMS, or NRSPMS who completed the Phase 2b LTS (LTS16004) or 1 of the 4 Phase 3 pivotal tolebrutinib trials (EFC16033, EFC16034, EFC16645, EFC16035) on IMP. OR \- The Phase 2b LTS (LTS16004) or Phase 3 tolebrutinib pivotal trial participants who tempo...