SAR441344 IV: Pharmaceutical form: Solution Route of administration: IV infusion
placebo IV: Pharmaceutical form: Solution Route of administration: IV infusion
SAR441344 SC: Pharmaceutical form: Solution Route of administration: SC injection
placebo SC: Pharmaceutical form: Solution Route of administration: SC injection
MRI contrast-enhancing preparations: gadolinium compound, including but not limited to Magnevist, Multihance, Prohance, or Elucirem
Study summary
Primary Objective:
To determine the efficacy of SAR441344 as measured by reduction of the number of new active brain lesions
Secondary Objective:
* To evaluate efficacy of SAR441344 on disease activity as assessed by other MRI measures
* To evaluate the safety and tolerability of SAR441344
* To evaluate pharmacokinetics of SAR441344
Eligibility
Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
No
Inclusion criteria:
* Participant must be 18 to 55 years of age inclusive, at the time of signing the informed consent.
* The participant must have been diagnosed with RMS (relapsing-remitting MS and secondary progressive MS participants with relapses) according to the 2017 revision of the McDonald diagnostic criteria.
* The participant must have at least 1 documented relapse within the previous year, or ≥2 documented relapses within the previous 2 years, or ≥1 active Gd-enhancing brain lesion on an MRI scan in the past 6 months and prior to screening.
* Body weight within 45 to 120 kg (inclusive) and body mass index (BMI) within the range 18.0 to 35.0 kg/m2 (inclusive) at Screening.
* Contraceptive use by men and women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
* Capable of giving signed informed consent.
Exclusion criteria:
* The participant was diagnosed with PPMS according to the 2017 revision of the McDonald diagnostic criteria or with non-relapsing SPMS.
* The participant had conditions or situations that would adversely affect participation in this study.
* The participant had a history of or currently has concomitant medical or clinical conditions that would adversely affect participation in this study.
* History, clinical evidence, suspicion or significant risk for thromboembolic events, as well as myocardial infarction, stroke and/or antiphosholipid syndrome and any participants requiring antithrombotic treatment.
* Allergies to humanized monoclonal antibodies or severe post-treatment hypersensitivity reactions other than localized injection site reaction, to any biological molecule.
* The participant had received any of the forbidden medications/treatments within the specified time frame before any baseline assessment.
* The participant had taken other investigational drug within 3 months or 5-half-live, whichever is longer, before the screening visit.
* The participant had an EDSS score \>5.5 at the first screening visit.
* The participant had a relapse in the 30 days prior to randomization.
* Positive human immunodeficiency virus (HIV) serology (anti HIV1 and anti HIV2 antibodies) or a known history of HIV infection, active or in remission.
* Abnormal laboratory test(s) at Screening.
* Presence of Hepatitis B surface antigen (HBsAg) or anti-Hepatitis B core antibodies (anti-HBc Ab) at screening or within 3 months prior to first dose of study intervention.
* Positive Hepatitis C antibody test result at screening or within 3 months prior to starting study intervention.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Primary outcome measure(s)
Mean Number of New Gadolinium (Gd)-Enhancing T1--Hyperintense (GdE T1) Lesions at Week 12 Relative to Week 8 as Measured by Brain Magnetic Resonance Imaging (MRI) — Week 8 and Week 12 Cranial (brain) MRI was performed to identify number of new GdE T1-hyperintense lesions at Week 12 relative to Week 8 MRI. Central review was used to identify new GdE T1 lesions not present at the previous MRI scans.
Trial sites (37)
Facility
City
Region
Status
Center for Neurology and Spine- Site Number : 8400007
Phoenix
Arizona
University of South Florida Site Number : 8400001
Tampa
Florida
The Neurological Institute Site Number : 8400004
Charlotte
North Carolina
Medical College of Wisconsin- Site Number : 8400006
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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