Strategic Acquisitions Completed
Completed acquisition of Bako Diagnostics and StrataDx in Q1 2026, adding $2.6M of revenue in the quarter, more than doubling the pathology sales team, expanding Anatomic Pathology market presence, and expected to contribute ~ $53M to revenue in H2 2026.
Strong Cash Position Despite Uses
Ended Q1 with $604.7M in cash, cash equivalents, restricted cash and marketable securities; management forecasts ending 2026 cash of ~$636M (assuming receipt of delayed tax refund and no further extraordinary expenditure).
Therapeutic Pipeline Momentum (FID-007 & FID-022)
FID-007 completed Phase II enrollment (46 patients) with encouraging early efficacy/safety; selected for rapid oral presentation at ASCO; plan for end-of-Phase-II FDA meeting in H2 2026 and potential Phase III start in H1 2027. FID-022 has completed dose level 3 and is in dose escalation with MTD expected later in 2026.
Reiterated 2026 Revenue Guidance
Reiterated full-year 2026 revenue guidance of $350M (implying ~8.5% year-over-year growth) and provided segment revenue targets: Precision Diagnostics ~$168M, Anatomic Pathology ~$162M, Biopharma Services ~$20M.
AI and Product Innovation Progress
In-house EasioPath platform is ~100% visual across cases; launched dermatopathology AI auto-rotation tool in Q1; integrated Illumina TruPath Genome into new whole genome test to deliver comprehensive single-report genomic insights across 20,000 genes.
Regulatory/Market Win for Pharmacogenomics
Received MolDX approval and pricing for PGx test (DPYD) in Q1 and benefits from shifting clinical guidance (ASCO/NCCN/FDA trends) that increase addressable market for DPYD pharmacogenomic testing.
Share Repurchase and Lower Share Count
Repurchased 2.6M shares in Q1 and an additional 0.5M to date; updated forecasted average diluted share count for 2026 reduced from ~32M to ~29M, resulting in a $0.14 per-share impact to non-GAAP EPS guidance.