Clinical EfficacyPhase 2 head-to-head data showed numerically superior efficacy and a clean safety profile versus the established anti-IgE therapy, supporting progression to pivotal trials.
Dosing DurabilityDemonstrated extended drug half-life supports less frequent dosing such as quarterly injections, which could improve patient convenience, adherence, and reduce the need for dose escalation.
Funding And Regulatory PathwayA substantial equity raise strengthened the balance sheet and, combined with planned FDA discussions on Phase 3 design, positions the company to initiate pivotal studies with a streamlined regulatory path.