- Milestone Pharmaceuticals Inc MIST announced topline efficacy and safety data from the Phase 3 RAPID clinical trial of etripamil for paroxysmal supraventricular tachycardia (PSVT), a type of abnormal heart rhythm (arrhythmia).
- The RAPID trial achieved its primary endpoint, with patients taking etripamil demonstrating a highly statistically significant and clinically meaningful difference in time to PSVT conversion compared to placebo.
- A statistically significantly greater proportion of patients who took etripamil converted within thirty minutes compared to placebo (64.3% vs. 31.2%).
- In addition, the median time to conversion for patients in RAPID who took etripamil was three times faster thaan for patients who took the placebo.
- The safety and tolerability data from the RAPID trial continue to support the potential self-use of etripamil, with findings consistent with those observed in prior trials.
- Analyses of pooled data from the NODE-301 and RAPID trials show that etripamil treatment provided a statistically significant reduction in the use of additional medical interventions and a statistically significant reduction in visits to the emergency department.
- The Company believes results from the RAPID trial and data from the already completed NODE-301 trial could fulfill the efficacy requirement for FDA marketing application submission, expected in mid-2023.
- Price Action: MIST shares are up 21.30% at $10.30 during the premarket session on the last check Monday.
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