T2 Biosystems Inc (TTOO) Q3 2024 Earnings Call Highlights: Revenue Surge and Strategic Partnerships Propel Growth

T2 Biosystems Inc (TTOO) reports a 34% revenue increase, driven by sepsis test sales and a pivotal partnership with Cardinal Health, despite ongoing financial challenges.

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Nov 15, 2024
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Release Date: November 14, 2024

For the complete transcript of the earnings call, please refer to the full earnings call transcript.

Positive Points

  • T2 Biosystems Inc (TTOO, Financial) reported a 34% increase in third-quarter revenue compared to the prior year, driven by strong sales of sepsis test panels.
  • The company executed contracts for 11 T2 DX instruments, with significant international sales growth of 78% compared to the previous year.
  • T2 Biosystems Inc (TTOO) entered into an exclusive commercial distribution agreement with Cardinal Health, which is expected to significantly expand their access to over 6,000 US hospitals.
  • The company is actively advancing its product pipeline, with several programs receiving FDA breakthrough device designation, including the T2 Resistance Panel.
  • Operational improvements include converting 80% of debt to common stock, reducing quarterly interest payments, and implementing cost-saving measures such as consolidating real estate space.

Negative Points

  • T2 Biosystems Inc (TTOO) reported a net loss of $10.1 million for the third quarter of 2024, although this was an improvement from the previous year's loss.
  • The company received a notice from NASDAQ indicating that its market value had been trading below listing requirements, prompting an appeal.
  • Despite revenue growth, the cost of product revenues increased by 4%, driven by higher international instrument and sepsis test sales.
  • Selling, general, and administrative expenses decreased by only 10%, partially offset by increased legal expenses.
  • The company continues to rely on raising capital through its ATM facility and is exploring other sources of capital, indicating ongoing financial challenges.

Q & A Highlights

Q: Has Cardinal Health already started marketing T2 Biosystems' products, and what impact do you expect this partnership to have on the fourth quarter financials? Additionally, do you anticipate a shift in instrument sales towards the U.S. due to this partnership?
A: Yes, Cardinal Health has begun marketing T2 Biosystems' products. We expect this partnership to increase our instrument and consumable sales in the U.S. significantly. Cardinal Health's extensive reach and credibility in U.S. hospitals make them an ideal partner, and we anticipate this collaboration will have a significant impact in 2025, with potential effects in the fourth quarter of 2024. (John Sperzel, CEO)

Q: Regarding the Lyme Disease Test (LDT), should we expect it to contribute to top-line revenue in the first half of 2025?
A: Yes, that is our plan. The Lyme disease season typically starts around April or May, so we are targeting the latter half of the second quarter for launching the LDT. (John Sperzel, CEO)

Q: Can you elaborate on the strategic importance of the partnership with Cardinal Health?
A: Cardinal Health is a significant partner due to their presence in over 90% of U.S. hospitals and their strong commercial organization. Their exclusive rights to our products provide them with a competitive advantage, and their credibility with hospitals is expected to drive significant growth in our U.S. market presence. (John Sperzel, CEO)

Q: What are the expected financial impacts of the operational changes, such as the consolidation of real estate and the partnership with ADP TotalSource?
A: We expect to save approximately $1 million annually from consolidating our real estate space and at least $400,000 annually from partnering with ADP TotalSource for HR solutions. These changes are part of our efforts to strengthen our cash position and improve our cost structure. (John Sperzel, CEO)

Q: What is the status of the T2 Resistance Panel and its path to FDA submission?
A: The T2 Resistance Panel, which detects 13 antibiotic resistance genes, is expected to be submitted to the FDA for 510(k) clearance in the first quarter of 2025. This submission was delayed by one quarter to prioritize manufacturing for current and new customers. (John Sperzel, CEO)

For the complete transcript of the earnings call, please refer to the full earnings call transcript.