Earlier this week, Active Biotech, based in Lund, Sweden, announced that it was abandoning its neurology focus, including MS. The overall focus is on the company’s wholly-owned lead assets, laquinimod and tasquinimod. Laquinimod is an oral small molecule developed primarily for neurodegenerative diseases like multiple sclerosis (MS) and Huntington’s disease (HD). It was in three completed Phase III trials in relapsing-remitting MS (RRMS) and a single Phase II trial in Huntington’s. The drug showed a consistent effect on endpoints and MRI parameters in RRMS as well as a “pronounced effect on brain atrophy” in both RRMS and HD. However, on July 31, 2018, the drug failed the Phase II LEGATO-HD clinical trial in HD. And in December 2017, its Phase II proof-of-concept study in Primary Progressive MS did not meet the primary endpoint.
They are going to focus their laquinimod work on Crohn’s disease and their tasquinimod work on multiple myeloma.
In December 2019, Adamas Pharmaceuticals reported that its Phase III INROADS trial of Gocovri (ADS-5102) for multiple sclerosis (MS) with walking impairment met its primary endpoint. That would seem to be good news, but the trial failed to meet secondary measures which worried investors, causing shares to drop by 45%.
Gocovri was approved by the U.S. Food and Drug Administration (FDA) for the treatment of dyskinesia in patients with Parkinson’s disease receiving levodopa-based therapy. It is not approved for MS with walking impairment.
The primary endpoint of the study was a 20% improvement in walking speed from baseline to 12 weeks post-treatment. This was measured by the Timed 25 Foot Walk. The patients taking 274 mg of the drug had a statistically significant improvement in response rate of 21.1% compared to 11.3% in patients taking the placebo. At a lower dose of 137 mg, the response was 17.6%.
However, key secondary endpoints included mean change in the Timed 25-Foot Walk, the Timed Up and Go, and the 2-Minute Walk at 12-week post-treatment at both doses. The drug did not show a significant effect on any of those measures at either dose.
Of the 48 New Drug Entities approved by the U.S. Food and Drug Administration (FDA) in 2019, only one was for MS. This was Novartis’ Mayzent (siponimod), for adults with relapsing forms of multiple sclerosis (MS).
“One of the most important aims of MS treatment is delaying disability progression and preserving cognition,” said Paul Hudson, Novartis Pharmaceuticals’ chief executive officer. “With Mayzent, SPMS patients with active disease will have access to the first effective oral therapy directed towards disease progression, even when MS transitions to a stage where deterioration is less dependent on the usual relapse activity.”
A Product Manager with expertise in pharma marketing and sales operations