Otsuka, Ionis’ experimental ALS drug meets main goal in late-stage study

Sept 22 (Reuters) – Otsuka Pharmaceutical and Ionis Pharmaceuticals said on Tuesday their experimental drug met the main goal of a late-stage study in patients with a rare inherited form of amyotrophic lateral sclerosis, or ALS.

Here are more details:

• Otsuka’s ulefnersen improved function and survival compared with placebo in patients with FUS-ALS, a rare inherited form of the disease that damages nerve cells controlling movement.

• There are currently no approved treatments specifically targeting the genetic cause of FUS-ALS.

• The drug also reduced markers linked to nerve cell damage and delayed disease progression.

• Most side effects were mild or moderate, and the companies said the drug showed a favorable safety profile.

• Otsuka and Ionis plan to discuss the results with the US FDA and other health authorities globally as they pursue potential accelerated approval pathways.

• FUS-ALS causes progressive muscle weakness that can leave patients unable to move, speak, swallow or breathe independently.

• Otsuka’s ulefnersen is an experimental medicine designed to reduce production of the FUS protein linked to the disease.

• Separately, Otsuka launched a global early access program for eligible FUS-ALS patients who cannot participate in clinical trials, allowing physicians to request access to ulefnersen before any potential approval.

(Reporting by Sahil Pandey in Bengaluru; Editing by Leroy Leo)