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Atossa Therapeutics announced the acceptance of a manuscript for publication in Degenerative Neurological and Neuromuscular Disease detailing new research into (Z)-endoxifen as a potential therapy for Duchenne muscular dystrophy.
The manuscript explores how (Z)-endoxifen may modulate utrophin-associated pathways, which are critical in addressing the progression of Duchenne muscular dystrophy. This step underscores a growing focus on innovative strategies to combat rare neuromuscular disorders.
Atossa previously announced new FDA rare disease designations alongside clinical advancements in its Q1 2026 financial results. The company has also explored (Z)-endoxifen as an endocrine therapy for breast cancer in a virtual event featuring key opinion leaders. These activities reflect the company's ongoing focus on developing novel therapies for challenging disease areas.