BI
BIOCEPT INC (BIOCQ)·Q3 2022 Earnings Summary
Executive Summary
- Q3 2022 revenue fell sharply as COVID-19 testing waned; net revenues were $5.59M and diluted EPS was -$0.33, with gross margin negative due to costs exceeding revenue .
- CNSide traction continued: orders rose 8% sequentially and 176% YoY, and 28 of 64 NCI-designated cancer centers had ordered; management sizes the CNSide TAM at ~$1.2B U.S./$2.0B global .
- Guidance narrative reiterated focus on CNSide clinical utility and reimbursement; COVID-19 testing revenue expected to end after December 2022 (first disclosed in Q2) .
- Near-term stock catalysts: CNSide clinical evidence (FORESEE trial site expansions) and broader center adoption; headwinds include payor liabilities and rapid COVID revenue decay .
What Went Well and What Went Wrong
What Went Well
- CNSide momentum: “CNSide orders increased 8% sequentially and 176% versus 3Q 2021” and multiple scientific posters featured at SNO, supporting clinical adoption narrative .
- Channel expansion: “28 of the elite 64 National Cancer Institute-designated cancer centers having ordered CNSide,” validating institutional interest .
- Cost control in SG&A and Sales: G&A fell to $3.0M (from $3.5M YoY); Sales & Marketing fell to $1.0M (from $1.9M YoY), reflecting reduced commissions and lower headcount .
What Went Wrong
- Revenue compression: Net revenues dropped to $5.59M from $17.47M YoY as COVID testing volumes fell (COVID revenue $4.7M vs. $16.5M a year ago) .
- Negative gross margin: Cost of revenues ($5.78M) exceeded revenue in Q3, yielding gross margin of -3.4% and EBIT margin near -100%, highlighting operating deleverage .
- Payor/HRSA headwinds: A $5.7M liability was recorded in Q2 due to HRSA recoupment mechanism changes; payor liability stood at $6.105M on Q3 balance sheet, elevating near-term cash dynamics risk .
Financial Results
Segment/Revenue Mix
Balance Sheet Liquidity
KPIs and Commercial Traction
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “Our third quarter financial results reflect solid increases in CNSide orders, up 8% sequentially and 176% year-over-year. We are executing well on our strategy to generate further evidence to secure higher reimbursement for CNSide and support its adoption into clinical care guidelines.” — Samuel D. Riccitelli, Interim President & CEO .
- “Our customer base has also expanded with 28 of the elite 64 National Cancer Institute-designated cancer centers having ordered CNSide… We estimate the annual market opportunity of $1.2 billion in the U.S. and $2 billion globally.” — Sam Riccitelli, Q3 call .
- “The first site in our FORESEE clinical trial is now open for patient enrollment and we expect at least one additional site to be cleared for enrollment in the coming months.” .
Q&A Highlights
- Adoption breadth and depth: Analyst questions probed how Biocept engages remaining NCI centers; management emphasized KOL outreach, medical team collaboration, and “relatively small commercial organization… not fully covering the geography,” indicating prioritized regional focus .
- Repeat orders: Management cited “relatively good performance” with increasing cases per client, underscoring stickiness post initial clinician experience .
- Financial reporting status: CFO noted current with quarterly SEC filings and focused remarks on Q3 and nine months results, aligning reported figures across press release and 10-Q .
Estimates Context
- Wall Street consensus (S&P Global) for Q3 2022 was unavailable due to missing CIQ mapping for BIOCQ in SPGI’s company map; therefore, we cannot benchmark Q3 revenue or EPS against S&P Global consensus. If you can supply a CIQ identifier, we will retrieve and compare consensus immediately [GetEstimates error].
Key Takeaways for Investors
- CNSide is the core growth asset; adoption continues across top cancer centers, with supportive scientific visibility (SNO posters) and expanding clinical evidence (FORESEE), underpinning a path to improved reimbursement and guideline inclusion .
- Revenue mix is transitioning rapidly away from COVID testing; investors should model near-zero COVID revenue after December 2022 and focus on CNSide volume growth, pricing/reimbursement, and payor contracts .
- Operating leverage deteriorated in Q3 as volumes fell; cost discipline in SG&A/Sales helped but gross margin turned negative—near-term profitability depends on CNSide scaling and reimbursement wins .
- Billing/collections risk remains elevated given payor liability exposures; monitor resolution timelines and balance sheet cash trends (cash down to $18.0M at Q3) .
- Biopharma collaborations (first CNSide trial revenue in Q2) illustrate an additional monetization route; expanding licensing/partner testing could diversify revenue beyond diagnostics services .
- Tactical actions: watch for updates on additional FORESEE sites, payer agreements, and NCI center onboarding; these are likely catalysts for estimate revisions and sentiment .
- Without S&P Global consensus, sell-side anchoring may be limited; expect shares to trade on execution signals (CNSide orders, center penetration, reimbursement milestones) rather than near-term quarterly beats/misses.
Sources
- Q3 2022 8‑K 2.02 and Exhibit 99.1 press release and financials:
- Q2 2022 8‑K 2.02 and Exhibit 99.1 press release and financials:
- Q1 2022 8‑K 2.02 and Exhibit 99.1 press release and financials:
- Q3 2022 earnings call transcript (InsiderMonkey):
- BusinessWire press release (Q3 2022 results):
- UCSF investigator-initiated study press release (Nov 16, 2022):