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Data validated efficacy and safety and informs dosing strategy for Phase 3 program
Achieved key co-primary endpoint on efficacy, with 500U dose demonstrating statistically significant difference from placebo in the Modified Ashworth Score (MAS) improvement from baseline
Numerical improvement compared with placebo achieved with all three doses on the Physician Global Impression of Change (PGIC) assessment, but did not reach statistical significance with the studys reduced enrollment due to COVID-19
Median duration of response of at least 24 weeks demonstrated in all three doses (250U, 375U, 500U)
Treatment was generally safe and well... More

