How the company describes its CNS oncology platform. Name changed Aug 3, 2026.
A laboratory-developed test. Performed at more than 120 U.S. cancer institutions, per the company.
Investigational and not FDA-approved. Topline data expected mid‑2027.
222 tests billed in Q3. Contracted commercial and Medicare Advantage lives, per the company.
Forward-looking statements, including trial timing and results and CNSide coverage, reimbursement and billing, involve risks; actual results may differ materially. REYOBIQ is investigational and not FDA-approved. Billings are unaudited gross billings. See SEC filings for risk factors.