Earnings Call Summary | Achieve Life(ACHV.US) Q1 2024 Earnings Conference
Earnings Call Summary | Achieve Life(ACHV.US) Q1 2024 Earnings Conference
The following is a summary of the Achieve Life Sciences, Inc. (ACHV) Q1 2024 Earnings Call Transcript:
以下是 Acheive Life Sciences, Inc. (ACHV) 2024 年第一季度财报电话会议记录摘要:
Financial Performance:
财务业绩:
Achieve Life Sciences reported having cash, cash equivalents, and restricted cash totaling $66.4 million as of March 31, 2024.
The company has secured up to $124 million in financing, providing cash coverage through the NDA submission, approval, and beyond, projecting a cash runway into the second half of 2025.
The company's total operating expenses in Q1 2024 were $6 million, compared to the $8.6 million in Q1 2023, marking a significant decrease.
A net loss of $6.5 million was reported for Q1 2024, which is less than the net loss of $9 million reported in Q1 2023.
Achieve Life Sciences报告称,截至2024年3月31日,现金、现金等价物和限制性现金总额为6,640万美元。
该公司已获得高达1.24亿美元的融资,通过保密协议提交、批准及其他方式提供现金保障,预计现金流将持续到2025年下半年。
该公司在2024年第一季度的总运营支出为600万美元,而2023年第一季度的总运营支出为860万美元,显著下降。
2024年第一季度报告的净亏损为650万美元,低于2023年第一季度报告的900万美元净亏损。
Business Progress:
业务进展:
There has been an agreement with the FDA concerning the necessary long-term cytisinicline exposure data for the NDA filing, which is planned to be submitted in the first half of 2025.
Recent clinical data indicates cytisinicline's effectiveness in aiding in smoking and vaping cessation.
Enrollment for the ORCA-OL, an open-label study designed to provide safety data on long-term cytisinicline use, is expected to begin in the following weeks.
Phase 2 ORCA-V1 trial results show cytisinicline may be the first FDA-approved treatment specifically for e-cigarette cessation, with plans to discuss the expansion into e-cigarette cessation indication with the FDA in future meetings.
The initiation of prospective enrollment in the ORCA-OL trial is anticipated.
The company received confirmation that a separate long-term exposure trial for a vaping indication isn't required.
已与美国食品药品管理局就保密协议申请所需的长期胞嘧啶暴露数据达成协议,该数据计划于2025年上半年提交。
最近的临床数据表明,胞嘧啶在帮助戒烟和戒烟方面有效。
ORCA-OL是一项开放标签研究,旨在提供长期使用胞嘧啶的安全数据,预计将在接下来的几周内开始入组。
ORCA-V1 第二阶段试验结果显示,胞嘧啶可能是美国食品药品管理局批准的第一种专门用于电子烟戒烟的治疗方法,并计划在未来的会议上与美国食品药品管理局讨论扩大电子烟戒烟适应症的问题。
预计ORCA-OL试验的前瞻性注册将开始。
该公司已得到证实,不需要针对电子烟适应症进行单独的长期暴露试验。
More details: Achieve Life IR
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