The next major valuation test is clinical, not another routine quarter. Interim Phase 2b data for ARS-2 in chronic spontaneous urticaria is now expected in Q1 2027. The program could expand the platform into an area with no FDA-approved on-demand treatment for acute flares, but the filing provides no efficacy result yet; for now, it is an option value rather than delivered evidence. (Expanding the Intranasal Epinephrine Platform)
Read the original 8-K on SEC EDGAR ↗