PI
Precipio, Inc. (PRPO)·Q3 2015 Earnings Summary
Executive Summary
- PRPO (Transgenomic, Inc. in 2015) reported Q3 2015 continuing operations net sales of $3.96M, down 3% year over year, with gross margin improving to 45%; total EPS was $(0.55), with continuing operations EPS of $(0.62) impacted by a $7.0M non-cash impairment and a $1.0M accrual reversal .
- Structural portfolio actions dominated the quarter: sale of the ion chromatography product line for ~$2.1M cash and a binding term sheet to divest the Genetic Assays & Platforms (GAP) unit (expected to reduce quarterly expenses by ~$1.2M) .
- Management emphasized accelerating commercialization of Multiplexed ICE COLD-PCR (MX-ICP), launching new liquid biopsy tests/panels, the first commercial license (University of Melbourne), and a pharma pilot study; year-to-date laboratory business up 18% on a stand‑alone basis despite seasonal/one-time factors .
- Cash was $2.8M at quarter-end; Q3 financing raised ~$2.7M net and asset sale added ~$2.1M; management signaled burn-rate near ~$2M in Q1 2016 pending revenue uptake from MX-ICP .
- Key stock reaction catalysts: accelerated MX-ICP commercialization/licensing, cost base reset from divestitures, and clarity around non-GAAP impairment effects and forward burn-rate trajectory .
What Went Well and What Went Wrong
What Went Well
- “We are very pleased with the increasing momentum we are achieving with MX-ICP… now can focus our full resources and energies on commercializing this technology” (CEO); three new liquid biopsy diagnostic tests and ICEme mutation enrichment kits launched; first commercial MX-ICP license secured in Australia .
- Gross margin improved to 45% (vs. 42% YoY) driven by lower operating supply costs; Modified EBITDA loss narrowed to $(1.3)M from $(3.1)M YoY, highlighting underlying operating improvements despite restructuring .
- Asset monetization and financing strengthened liquidity: ~$2.1M columns sale and ~$2.7M net financing, supporting commercialization and reducing legacy distractions .
What Went Wrong
- $7.0M non-cash impairment in Patient Testing long‑lived assets, with continuing ops EPS of $(0.62); even excluding impairment and $1.0M accrual reversal, continuing ops EPS was $(0.18) reflecting ongoing losses .
- Contract lab services down ~$0.2M as legacy pharma services transition to ICE COLD-based offerings; seasonal and one-time factors obscured standalone lab business growth .
- QoQ reported net sales declined versus Q2 levels as GAP moved to discontinued operations and structural changes reduced consolidated revenue visibility; burn-rate guidance implies continued cash usage into early 2016 absent faster MX-ICP ramp .
Financial Results
Notes:
- Q3 2015 and Q3 2014 reflect continuing operations with GAP treated as discontinued; Q1/Q2 2015 did not break out continuing vs discontinued in press release 8-Ks .
Segment and Drivers (disclosed elements)
KPIs and Balance Sheet
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- CEO on strategic focus: “We are very pleased with the increasing momentum we are achieving with MX-ICP… with our new streamlined structure, we now can focus our full resources and energies on commercializing this technology” .
- CEO on commercialization milestones: “We launched three new liquid biopsy diagnostic tests… announced a new pilot study with four leading biopharmaceutical firms… presented data… with Amgen… announced our first commercial MX-ICP license” .
- CAO on financials: “Gross profit was 1.8 million or 45%… Operating expenses were 10.7 million… includes $7 million impairment… reversal of an accrual liability of 1 million… net loss from continuing operations… $8.2 million or $0.62 per share” .
- CEO on laboratory business and seasonality: “Our laboratory business is up 18% this year on a stand‑alone basis, but these gains were obscured in the third quarter due to seasonal and one-time factors” .
Q&A Highlights
- ICE COLD-PCR revenue timing: Management expects a “sizeable” contribution by year-end across licensing, CLIA testing, and kits; ramp to become a “major number” in 2016 as commercialization scales .
- Expense reduction drivers: Savings reflect both divestitures and tighter cost control; cash flow benefits expected to be more visible in 2016 as transactions close .
- Burn-rate outlook: Burn in Q1 2016 guided to “maybe… ~$2 million,” with profitability leverage as fixed-cost lab capacity is utilized .
Estimates Context
- Wall Street consensus (S&P Global) for Q3 2015 and Q2 2015 was unavailable at time of query; therefore, beat/miss analysis versus estimates cannot be provided. Consensus data unavailable (S&P Global)*.
Key Takeaways for Investors
- Near-term stock narrative centers on MX-ICP commercialization momentum (new tests/panels, first license, pharma pilot) and the strategic exit from legacy GAP/columns businesses to streamline focus .
- Reported results include significant non-GAAP items (impairment and accrual reversal); underlying margins and Modified EBITDA are improving, suggesting operating progress beneath restructuring noise .
- Liquidity improved via financing and asset sales; burn-rate guidance (~$2M in Q1 2016) sets expectations for additional capital or accelerated revenue ramp from MX-ICP to bridge to breakeven .
- Revenue mix is shifting toward patient testing and contract services aligned with ICE COLD-PCR; expect volatility as legacy revenue winds down and new offerings ramp .
- Watch for incremental licensing deals, clinical validation publications, and pharma services conversions from the pilot study—key catalysts for 2016 revenue and margin expansion .
- Expense reductions (> $1M/quarter; GAP divestiture ~$1.2M quarterly impact) should structurally lower the cost base, amplifying operating leverage as MX-ICP volumes grow .
- With consensus estimates unavailable, trading setups will hinge on qualitative catalysts and sequential progress metrics (test launches, contracts, cash burn trajectory) until visibility improves (S&P Global)*.
Footnote: *Consensus data unavailable (S&P Global).