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Low Temelimab Doses of RRMS Trial Among Reasons for Poor Results
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Safety Board Says Phase 2 Temelimab Trial for MS Should Move Forward
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GeNeuro Completes Enrollment in Phase 2 Trial Testing Temelimab in MS
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> Nachricht GeNeuro Completes Patient Recruitment in Temelimab Phase 2 Multiple Sclerosis Trial at the Karolinska Institutet’s Academic Specialist Center (ASC) Regulatory News: GeNeuro (Euronext Paris: CH0308403085 - GNRO), a biopharmaceutical company focused on stopping causal factors driving the progression of neurodegenerative and autoimmune diseases, such as multiple sclerosis (MS), today announced the completed patient recruitment in its Phase 2 trial of temelimab in MS patients, conducted at the Karolinska Institutet’s Academic Specialist Center (ASC), in Stockholm (Sweden). Temelimab is a monoclonal antibody designed to neutralize a pathogenic retroviral envelope protein, pHERV-W Env. The study, called ProTEct-MS, has enrolled a very homogenous cohort of 42 patients being treated with temelimab (18, 36 and 54mg/kg) vs. placebo and evaluated for 48 weeks. The patients included in