GeNeuro Announces Positive Results from Temelimab (GNbAC1) Phase 1 High-dose Clinical Trial

GeNeuro Announces Positive Results from Temelimab (GNbAC1) Phase 1 High-dose Clinical Trial

International Nonproprietary Name "temelimab" Assigned to GNbAC1

Temelimab’s robust safety and tolerability profile confirmed

High-dose regimen fully validated by pharmacokinetic data

Enables higher doses or front-loading to be considered for future clinical studies

Drug candidate’s overall profile enhanced ahead of a possible partnership to continue the global development of temelimab as a treatment for multiple sclerosis (MS)

International Nonproprietary Name "temelimab" assigned by the WHO for GNbAC1

Geneva, Switzerland, 21 January 2019 – 6.00pm CET – GeNeuro (Euronext Paris: CH0308403085 - GNRO), a biopharmaceutical company developing new treatments for neurological and autoimmune diseases such as multiple sclerosis (MS) and type-1 diabetes, today announced positive safety and tolerability results from a Phase 1 study assessing the administration of high doses of temelimab (GNbAC1) to treat MS and other auto-immune diseases.

http://www.geneuro.com/data/news/GeNeuro-PR-Phase-I-dose-elevee-EN.pdf