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IceCure Medical Ltd (ICCM) Q3 2024 Earnings Call Transcript Summary

IceCure Medical Ltd (ICCM) Q3 2024 Earnings Call Transcript Summary

IceCure醫療有限公司(ICCM)2024年第三季度業績會簡報
富途資訊 ·  11/27 03:01  · 電話會議

The following is a summary of the IceCure Medical Ltd (ICCM) Q3 2024 Earnings Call Transcript:

以下是IceCure Medical Ltd (ICCM) 2024年第三季度業績會的摘要:

Financial Performance:

財務表現:

  • ProSense systems and disposable probe sales increased by 36% to $2.32 million for the nine months ending September 30, 2024, compared to the previous year.

  • Total revenue grew by 22% to $2.42 million in the same period, driven by higher sales in Europe, the US, and Japan.

  • Gross profit increased by 41% to $1.03 million, and gross margin improved to 43% from the previous year's 37%.

  • ProSense系統和一次性探頭的銷售額增長了36%,達到232萬美元,截止到2024年9月30日的九個月裏,相比於去年。

  • 總營業收入在同一時期增長了22%,達到了242萬美元,得益於在歐洲、美國和日本的銷售增長。

  • 毛利潤增長了41%,達到103萬美元,毛利率從去年的37%改善至43%。

Business Progress:

業務進展:

  • Completed the ICE3 trial with positive outcomes, potentially leading to FDA marketing authorization for ProSense.

  • Engaged in the PRECISE study, financed by the Umberto Veronesi Foundation and the Italian Ministry of Health, using ProSense in a larger patient population.

  • Partnered with Terumo Corporation in Japan to file for regulatory approval of ProSense for breast cancer in 2025.

  • 完成了ICE3試驗,並取得積極成果,可能導致FDA對ProSense的市場授權。

  • 參與了PRECISE研究,該研究由Umberto Veronesi基金會和意大利衛生部資助,使用ProSense在更大患者人群中進行。

  • 與日本的Terumo Corporation合作,計劃於2025年申請ProSense用於乳腺癌的監管批准。

Opportunities:

機會:

  • The potential FDA authorization of ProSense in Q1 2025 could significantly boost the U.S. market presence.

  • Upcoming catalysts in 2025 include interim results from the ICESECRET study and additional regulatory approvals in Japan.

  • 2025年第一季度ProSense潛在的FDA授權可能會顯著提升其在美國市場的影響力。

  • 2025年即將發生的催化劑包括ICESECREt研究的中期結果和日本的額外監管批准。

Risks:

風險:

  • There remains uncertainty regarding the exact timing for FDA marketing authorization and the approach of the FDA in terms of special controls and post-marketing requirements.

  • 關於FDA市場授權的確切時間以及FDA在特殊控制和市場後要求方面的做法仍存在不確定性。

Tips: For more comprehensive details, please refer to the IR website. The article is only for investors' reference without any guidance or recommendation suggestions.

提示:如需更全面的詳情,請參閱投資人關係網站。本文僅供投資者參考,不作任何指引或建議。

譯文內容由第三人軟體翻譯。


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