Clinical ResultsIgalmi's highest-approved 180µg dose showed no signs of tolerance, tachyphylaxis, or withdrawal in an open-label PMR study involving inpatient adults with frequent episodes of agitation associated with schizophrenia or bipolar disorder.
Market ExpansionImportant implications are expected from the post-marketing requirement study, which could expand the use and commercialization of the product.
Treatment PotentialThe stock affords the potential for significant upside if the company is able to successfully execute and develop the product for agitation in Alzheimer's disease where the unmet need is high.