Lisata Therapeutics, Inc. (LSTA) Q3 2024 Earnings Call Transcript Summary
Lisata Therapeutics, Inc. (LSTA) Q3 2024 Earnings Call Transcript Summary
The following is a summary of the Lisata Therapeutics, Inc. (LSTA) Q3 2024 Earnings Call Transcript:
以下是Lisata Therapeutics, Inc.(LSTA)2024年第三季度业绩会记录的摘要:
Financial Performance:
财务表现:
Lisata Therapeutics reported a decrease in operating expenses for Q3 2024, totaling $5.3 million compared to $6 million in the same period last year.
Research and development expenses decreased by 24.8%, largely due to reduced expenses in clinical research organization and lower equity expense associated with Phase IIa BOLSTER trial modifications.
General and administrative expenses saw an increase of 8.1%, attributed to higher consulting expenses.
Net losses improved to $4.9 million in Q3 2024 from $5.3 million in Q3 2023.
Lisata Therapeutics报告2024年第三季度营业费用减少,总计530万美金,相较于去年同一时期的600万美金。
研发费用减少了24.8%,主要由于临床研究组织的费用降低以及与第二期BOLSTER试验修改相关的股权费用减少。
一般和行政费用增加了8.1%,归因于咨询费用的增加。
净亏损在2024年第三季度改善至490万美金,相较于2023年第三季度的530万美金。
Business Progress:
业务进展:
Lisata is advancing the development of certepetide across multiple solid tumors including pancreatic, cholangiocarcinoma, and others, with ongoing and planned clinical trials such as the ASCEND and BOLSTER trials.
Significant regulatory designations have been achieved, including orphan drug and Fast Track designations, enhancing the development pathway for certepetide.
The company has initiated preclinical investigations of certepetide for non-oncological uses, specifically in the treatment of endometriosis, indicating a strategic expansion of the therapeutic applications of certepetide.
Lisata正在推进certepetide在多种固体肿瘤中的开发,包括胰腺癌、胆管癌等,并进行正在进行和计划中的临床试验,如ASCEND和BOLSTER试验。
已经取得了重要的监管认定,包括孤儿药和快速通道认定,增强了对certepetide的开发路径。
公司已启动对certepetide在非肿瘤用途方面的临床前研究,特别是在治疗子宫内膜异位症方面,这表明对certepetide治疗应用的策略扩展。
Opportunities:
机会:
Lisata continues to explore strategic partnerships and expand its development strategy in both oncologic and non-oncologic fields, leveraging existing clinical and preclinical collaborations to maximize the therapeutic potential of certepetide.
Lisata继续探索战略合作伙伴关系,并扩大其在肿瘤和非肿瘤领域的发展策略,利用现有的临床和临床前合作,最大化certepetide的治疗潜力。
Risks:
风险:
Slow initial enrollment rate in the GBM trial, particularly in Latvia, has posed challenges, despite optimization efforts. This might impact the timelines and expected outcomes of the trial.
尽管进行了优化努力,但在拉脱维亚,GBm试验的初始招募速度缓慢,这带来了挑战。这可能会影响试验的时间表和预期结果。
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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。