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Sep 30, 2024

Black Diamond Therapeutics Q3 2024 Earnings Report

Reported third quarter financial results and provided a corporate update.

Key Takeaways

Black Diamond Therapeutics reported its third quarter 2024 financial results, highlighting encouraging initial Phase 2 data of BDTX-1535 in recurrent EGFRm NSCLC and a corporate restructuring to prioritize BDTX-1535 development and extend cash runway into Q2 2026.

Announced encouraging initial Phase 2 data of BDTX-1535 in patients with recurrent EGFRm NSCLC in September 2024.

Presented real-world treatment practices and patient outcomes in newly diagnosed NSCLC patients with non-classical EGFR mutations at the 2024 ESMO Congress.

Clinical updates of BDTX-1535 in EGFRm NSCLC and regulatory feedback expected in Q1 2025.

Cash, cash equivalents, and investments of $112.7 million as of September 30, 2024; expected to be sufficient to fund operations into Q2 of 2026.

Total Revenue
$0
EPS
-$0.28
Previous year: -$0.45
-37.8%
Gross Profit
-$86K
Previous year: -$823K
-89.6%
Cash and Equivalents
$113M
Previous year: $144M
-21.9%
Free Cash Flow
-$11.3M
Previous year: -$18.4M
-38.4%
Total Assets
$138M
Previous year: $172M
-20.0%

Black Diamond Therapeutics

Black Diamond Therapeutics

Forward Guidance

Black Diamond expects to disclose initial Phase 2 data in first-line EGFRm NSCLC patients with non-classical mutations as well as updated Phase 2 results in the recurrent EGFRm NSCLC setting in Q1 2025. The company believes its cash, cash equivalents and investments will be sufficient to fund its anticipated operating expenses and capital expenditure requirements into the second quarter of 2026.

Positive Outlook

  • Potential for BDTX-1535 to address unmet medical need for newly diagnosed NSCLC patients with non-classical EGFR mutations.
  • Continued development and advancement of BDTX-1535, including ongoing clinical trials.
  • Expected timing for regulatory feedback and the disclosure of potential registrational pathways for BDTX-1535 in NSCLC.
  • Potential future development plans for BDTX-1535 in NSCLC and GBM.
  • Expected cost savings from the corporate restructuring plan.

Challenges Ahead

  • Uncertainties regarding the clinical development and regulatory approval of BDTX-1535.
  • Risks associated with potential delays or setbacks in clinical trials.
  • Uncertainties regarding the successful execution of the corporate restructuring plan.
  • Dependence on partnerships for BDTX-4933.
  • Potential impact of risks and uncertainties set forth in the company's filings with the SEC.