IceCure Medical (ICCM) Q2 2024 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2024 earnings summary
23 Jan, 2026Executive summary
ProSense system and probe sales grew 20% year-over-year in H1 2024, driven by adoption in Europe, the U.S., Japan, and Asia, with China sales at zero due to local factors.
Achieved all primary objectives for H1 2024, with strong patient and physician demand for minimally invasive breast cancer treatments.
Multiple independent studies confirm high efficacy and safety of ProSense, with 100% ablation rates and no major complications in key studies.
ProSense is approved for breast cancer in several global markets, with growing global demand and increasing adoption.
Preparing for FDA Medical Device Advisory Committee review in Q4 2024 for early-stage, low risk breast cancer indication.
Financial highlights
Total revenue for H1 2024 was $1.75 million, up from $1.65 million in H1 2023, mainly due to increased ProSense system and disposables sales.
Gross profit rose to $799,000 (GAAP) and $699,000 (non-GAAP), with non-GAAP gross margin improving to 42% from 35% year-over-year.
Operating expenses decreased to $7.68 million from $8.8 million, narrowing net loss to $6.7 million ($0.14/share) from $7.66 million ($0.17/share) year-over-year.
Cash and cash equivalents were $10.5 million as of June 30, 2024, and $10.3 million as of July 31, 2024.
Raised $5.035 million in gross proceeds from ATM facility in H1 2024.
Outlook and guidance
FDA advisory panel for ProSense in early-stage breast cancer expected in Q4 2024, with a marketing clearance decision anticipated in Q1 2025.
Terumo, the Japanese partner, plans to file for regulatory approval in Japan in Q1 2025.
Interim analysis of ICESECRET kidney cancer trial expected in December 2024.
Commercial rollout strategy in the U.S. post-FDA approval includes KOL engagement and society partnerships.
Additional third-party data on ProSense anticipated from ongoing global studies.
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