Celcuity Inc. (CELC) Q3 2024 Earnings Call Transcript Summary
Celcuity Inc. (CELC) Q3 2024 Earnings Call Transcript Summary
The following is a summary of the Celcuity Inc. (CELC) Q3 2024 Earnings Call Transcript:
以下是celcuity Inc. (CELC) 2024年第三季度业绩会议通话摘要:
Financial Performance:
财务表现:
Celcuity reported a net loss of $29.8 million, or $0.70 per share for Q3 2024, compared to a net loss of $18.4 million, or $0.83 per share for Q3 2023.
Non-GAAP adjusted net loss was $27.6 million, or $0.65 per share, compared to $17.3 million, or $0.78 per share, year over year.
Research and development expenses increased to $27.6 million, primarily due to activities supporting ongoing clinical trials.
Celcuity报告2024年第三季度净亏损$2980万,每股亏损$0.70,相比于2023年第三季度净亏损$1840万,每股亏损$0.83。
非通用会计准则调整后净亏损为$2760万,每股亏损$0.65,与去年相比$1730万,每股亏损$0.78。
研发费用增至$2760万,主要是由于支持进行中临床试验的活动增加。
Business Progress:
业务进展:
The VIKTORIA-1 Phase III clinical trial evaluating gedatolisib in breast cancer is progressing with the PIK3CA wild-type cohort fully enrolled and the mutant cohort on track.
Plans are on track to enroll the first patient in the VIKTORIA-2 Phase III trial in Q2 2025, which evaluates gedatolisib in a first-line setting.
Phase Ib/II trial evaluating gedatolisib in metastatic castration-resistant prostate cancer is also ongoing, with expected preliminary data in Q2 2025.
VIKTORIA-1第三期乳腺癌评估gedatolisib的临床试验正在进行中,PIK3CA野生型群体已招满,突变群体进展顺利。
计划按计划在2025年第二季度招募VIKTORIA-2第三期试验的第一名患者,该试验评估gedatolisib在一线设置中的应用。
目前,正在进行一项评估gedatolisib在转移性去势抵抗性前列腺癌中的Ib/II期试验,预计将于2025年第二季度公布初步数据。
Opportunities:
机会:
Potential market expansion with gedatolisib, targeting a peak revenue opportunity exceeding $2 billion if FDA approvals are granted for both PIK3CA wild-type and mutant populations.
Potential to establish a new standard of care in breast cancer management with a triplet regimen including gedatolisib, addressing three interconnected signaling pathways.
Favorable feedback on gedatolisib's IV route of administration, which could offer advantages in market access and therapy adherence.
如果FDA批准PIK3CA野生型和突变型人群,gedatolisib有潜力拓展市场,目标营收机会超过20亿美元。
使用包括gedatolisib在内的三联疗法有望在乳腺癌治疗中确立新的标准,涉及到三个相互关联的信号通路。
关于gedatolisib的静脉给药途径获得了良好的反馈,这可能在市场准入和治疗依从性方面带来优势。
Risks:
风险:
Delay in reaching the primary analysis event threshold for the clinical trial cohorts could impact the timeline for drug approval and market entry.
临床试验队列未达到主要分析事件门槛的延迟可能影响药物批准和市场准入的时间表。
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提示:本文由人工智能生成。内容准确性无法完全保证。如需更全面详情,请参阅IR网站。本文仅供投资者参考,不具有任何指导或推荐建议。