FDA Clears Phase 3b Trial of NurOwn for ALS
4 Articles
4 Articles
An Experimental Clinical Trial Achieved a Great Recovery in One ALS Patient
The new therapy was applied in only 12 patients and developed in the United States. It allowed reversing the effects of one of the most aggressive variants of amyotrophic lateral sclerosis, according to a study published in The Lancet
FDA clears Phase 3b trial of NurOwn for ALS
The U.S. Food and Drug Administration (FDA) has cleared a Phase 3b clinical trial to test Brainstorm Cell Therapeutics’ cell-based therapy NurOwn (debamestrocel) in people with amyotrophic lateral sclerosis (ALS). The trial, ENDURANCE (NCT06973629), is expected to open soon at more than a dozen sites across the U.S. It plans to recruit about 200 adults with moderate disease who have been experiencing symptoms of ALS, including muscle weakness, f…
Coverage Details
Bias Distribution
- 100% of the sources lean Left
To view factuality data please Upgrade to Premium
Ownership
To view ownership data please Upgrade to Vantage