Senior consultant neurologist Dr Angelina Hatlø Maniaol is coordinating investigator for the study, which will consist of a 6-month double-blind randomized phase where patients will get either Riluzole or ILB®, followed by a 6-month open-label extension where patients will get both ILB® and Riluzole.
The study is sponsored by Oslo University Hospital, funded by public research grants and is open to Norwegian residents only. TikoMed will supply ILB® for both study phases as well as corresponding placebo for the RCT.
The study has received all required regulatory approvals and is expected to start enrolling patients during the first quarter of 2026. Results are expected by the end of 2028.
More information is available on the Oslo University homepage (only in Norwegian):