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Turnstone Biologics Corp. (TSBX)·Q2 2024 Earnings Summary

Executive Summary

  • Q2 featured positive initial clinical data for TIDAL-01 in MSS metastatic colorectal cancer (25% ORR, 50% DCR; one ongoing CR >1 year), strengthening the program’s differentiation and providing a tangible clinical catalyst for sentiment and future data readouts .
  • Operating spend was controlled: R&D rose 2.9% YoY to $17.7M while G&A fell 8.5% YoY to $4.3M; net loss was $21.3M (vs. $21.5M LY) . Cash and investments were $62.4M with runway guided into 3Q25, maintained from Q1 .
  • Strategy sharpened: management prioritized CRC, HNSCC, and uveal melanoma and deprioritized cutaneous melanoma and breast cancer, focusing resources where the competitive profile appears strongest .
  • Financing overhang remains: substantial doubt as a going concern persists; the $20M revolver requires positive interim Phase 1 data (achieved Aug-24) and at least $40M of new funding by Mar 31, 2025, implying potential capital actions ahead .

What Went Well and What Went Wrong

  • What Went Well

    • Demonstrated clinical activity in hard-to-treat MSS mCRC: 25% ORR and 50% DCR in first four evaluable patients; one CR with PFS >1 year; TIDAL-01 generally well tolerated .
    • Manufacturing consistency: 80% manufacturing success rate for evaluable CRC patients with sufficient starting material; target dose ≥1×10^9 cells exceeded in all manufactured CRC products .
    • Focused portfolio execution: prioritization of CRC, HNSCC, and uveal melanoma to concentrate resources where Selected TIL approach may be most differentiated .
    • Management tone: “The clinical signals… including a remarkable complete response… support our fundamental hypothesis of enriching for tumor-reactive T cells in our Selected TIL therapies” – CEO Sammy Farah .
  • What Went Wrong

    • No product revenue; continued operating losses: Q2 net loss $21.3M; six-month net loss widened to $40.9M YoY due to prior-year collaboration revenue roll-off .
    • Capital risk: management disclosed substantial doubt about going concern and the need to raise additional capital; revolver covenant requires ≥$40M new funding by 3/31/25 .
    • Pipeline rationalization: deprioritization of cutaneous melanoma and breast cancer underscores resource constraints and the need to focus on highest-probability indications .

Financial Results

MetricQ2 2023Q1 2024Q2 2024
Revenue ($USD Millions)$0.0 $0.0 $0.0
R&D Expense ($USD Millions)$17.2 $15.8 $17.7
G&A Expense ($USD Millions)$4.7 $4.9 $4.3
Other Income ($USD Millions)$0.35 $1.08 $0.76
Net Loss ($USD Millions)$(21.5) $(19.6) $(21.3)
Diluted EPS ($)$(7.56) $(0.85) $(0.92)

Liquidity and Runway

MetricQ4 2023Q1 2024Q2 2024
Cash, Cash Equivalents & Short-term Investments ($USD Millions)$94.8 $77.8 $62.4
Runway GuidanceInto 2Q25 Into 3Q25 Into 3Q25

KPIs (Clinical and Manufacturing, Q2 2024)

KPIQ2 2024
ORR (MSS mCRC, first 4 evaluable)25%
DCR (MSS mCRC, first 4 evaluable)50%
DurabilityOne ongoing CR, PFS >1 year; one SD ~6 months
Manufacturing success rate (CRC, evaluable with sufficient starting material)80%
Dose target≥1×10^9 cells exceeded in all manufactured CRC products
SafetyGenerally well tolerated; AEs consistent with lymphodepletion, IL-2, and pembrolizumab

Context on YoY cost trends: R&D +2.9% YoY; G&A −8.5% YoY; net loss roughly flat YoY .

Guidance Changes

MetricPeriodPrevious GuidanceCurrent GuidanceChange
Cash runwayAs of Q4 2023 vs Q1 2024Into 2Q25 Into 3Q25 Raised
Cash runwayAs of Q1 2024 vs Q2 2024Into 3Q25 Into 3Q25 Maintained
Next clinical update for TIDAL-01Forward-lookingInitial mid-2024 update delivered; next update 1H 2025 1H 2025 Set next milestone
Indication focusProgram strategyBroader set incl. breast, cutaneous melanoma Prioritized CRC, HNSCC, uveal; deprioritized cutaneous melanoma & breast Refocused
Financing covenants (BOC revolver)Through 3/31/2025N/APositive interim Phase 1 data achieved Aug-24; ≥$40M new funding required by 3/31/25 New/active covenant

Earnings Call Themes & Trends

TopicPrevious Mentions (Q4 2023 and Q1 2024)Current Period (Q2 2024)Trend
Clinical efficacy signals (TIDAL-01)Anticipated initial data mid-2024 25% ORR, 50% DCR; ongoing CR >1 year in MSS mCRC Positive inflection
Manufacturing capacity/consistencyAdded cleanroom capacity at Moffitt for STARLING; CDMO capacity in place 80% CRC manufacturing success; dose target met/exceeded Execution improving
Indication strategyMultiple tumor types including breast & cutaneous melanoma Prioritized CRC, HNSCC, uveal; deprioritized breast/cutaneous melanoma Focused portfolio
Liquidity/runwayRunway into 2Q25 (YE23); into 3Q25 (Q1) Maintained 3Q25 runway Stable but declining cash
Capital structure/financingRevolver secured in April 2024 Covenant requires ≥$40M new funding by 3/31/25; going concern persists Financing need likely
Macro/supply chainMonitoring macro/geopolitical; no material impact cited Unchanged Stable

Note: No Q2 2024 earnings call transcript was furnished; the company provided results and clinical updates via 8-K press releases and investor materials .

Management Commentary

  • “The clinical signals from these initial data, including a remarkable complete response in one of the first four patients, demonstrated deep and durable anti-tumor activity… As the competitive profile of TIDAL-01 strengthens… we are prioritizing development in … CRC, head and neck cancer, and uveal melanoma.” — Sammy Farah, President & CEO .
  • “The encouraging initial clinical data… supports the potential of TIDAL-01 to transform the treatment paradigm for patients with metastatic CRC… we are extremely pleased by this positive start.” — Sammy Farah, President & CEO .
  • “The early evidence of clinical benefit highlights TIDAL-01 as a potential therapeutically viable option in metastatic CRC… the patient who experienced a complete response remains in remission and is well more than one year post treatment.” — Mike Burgess, Interim CMO .
  • Q1 setup: “We remain on track and plan to provide a TIDAL-01 clinical update mid-year … and look forward to generating clinical data to highlight the differentiation of our platform.” — Sammy Farah .

Q&A Highlights

  • Not applicable; the company did not furnish a Q2 2024 earnings call transcript with its 8-K filings. Results and clinical updates were communicated via press releases (Exhibits 99.1 and 99.2) .

Estimates Context

  • Wall Street consensus (S&P Global) for Q2 2024 EPS and revenue was unavailable for TSBX at the time of this analysis due to missing mapping/coverage; consequently, beat/miss versus consensus cannot be determined. We will monitor S&P Global data for future updates.

Key Takeaways for Investors

  • TIDAL-01 posted an early proof-of-concept in MSS mCRC (25% ORR, 50% DCR; ongoing CR >1 year), a setting with 1–6% ORR on current standards, supporting differentiation of Selected TILs and providing a clinical momentum catalyst into the next data update in 1H25 .
  • Portfolio focus (CRC, HNSCC, uveal) should concentrate spend on the most promising indications and streamline execution, while deprioritizing lower-priority settings (cutaneous melanoma, breast) .
  • Cash runway into 3Q25 offers near- to medium-term visibility, but going concern language and the revolver’s ≥$40M new funding covenant by 3/31/25 imply a probable financing or BD event within 12 months—an overhang to watch for trading .
  • Operating discipline evident: R&D modestly up YoY on TIDAL-01 manufacturing/clinical scale-up; G&A down YoY. However, absent revenue, net losses are likely to persist until a larger BD inflow or later-stage milestones .
  • Near-term stock drivers: additional patient accrual in prioritized indications, any interim data updates before 1H25, clarity on partnership activity, and any financing terms; watch the investor presentation updates as a signaling device .
  • Risk skew: financing and covenant risks, early-stage data set size (n=4 evaluable), manufacturing and clinical scalability; offset by early efficacy signal in a cold-tumor setting and a clearer strategic focus .

Supporting documents: Q2 2024 8-K (financial results and clinical data) ; Q2 2024 10-Q (full financials, MD&A, liquidity, covenants) ; Q1 2024 8-K (financials, manufacturing capacity) ; Q4 2023 8-K (baseline guidance, indications) .