Low Leverage / Balance SheetVery low reported debt provides structural financial flexibility versus many early-stage biotech peers, reducing near-term insolvency risk and giving management time to advance clinical programs. This durable strength helps sustain development activities while fundraising occurs.
Regulatory Engagement Advancing Phase 2bA formal FDA Type C meeting that clarified clinically meaningful endpoints materially reduces later-stage development execution risk. This durable regulatory progress strengthens the company’s path to a Phase 2b trial in DLB, improving likelihood of efficient trial design and regulator alignment.
Published Phase 2 Data For ZervimesinePeer-reviewed Phase 2 publication demonstrating safety and positive signals across behavioral, cognitive, functional, and movement domains provides durable scientific validation. This strengthens the biological rationale, de-risks later trials, and increases partnerability for out-licensing or collaborations.