Regulus Therapeutics Announces Participation at Upcoming Healthcare Investment Conferences
Regulus Therapeutics Announces Participation at Upcoming Healthcare Investment Conferences
SAN DIEGO, Nov. 26, 2024 /PRNewswire/ -- Regulus Therapeutics Inc. (Nasdaq: RGLS), a biopharmaceutical company focused on the discovery and development of innovative medicines targeting microRNAs (the "Company" or "Regulus"), today announced that the Company will participate in the following investor conferences:
圣地亚哥,2024年11月26日 /PRNewswire/ — 专注于发现和开发针对microRNA的创新药物的生物制药公司Regulus Therapeutics Inc.(“公司” 或 “Regulus”)今天宣布,该公司将参加以下投资者会议:
- Evercore 7th Annual HealthCONx Conference: Fireside chat on Tuesday, December 3, 2024, at 3:50 p.m. ET
- Piper Sandler 36th Annual Healthcare Conference: Presentation on Wednesday, December 4, 2024, at 11:10 a.m. ET
- Evercore 第七届年度 HealthConx 会议:美国东部时间 2024 年 12 月 3 日星期二下午 3:50 的炉边谈话
- 派珀·桑德勒第 36 届年度医疗保健会议:美国东部时间 2024 年 12 月 4 日星期三上午 11:10 的演讲
The live events and replays of the presentations will be available under "Events and Presentations" through the investor relations section of the Company's website at and archived for 90 days following the presentation date.
演示的现场活动和重播将在公司网站的投资者关系部分的 “活动和演讲” 下提供,并在演示日期后的90天内存档。
About Regulus
Regulus Therapeutics Inc. (Nasdaq: RGLS) is a biopharmaceutical company focused on the discovery and development of innovative medicines targeting microRNAs. Regulus has leveraged its oligonucleotide drug discovery and development expertise to develop a pipeline complemented by a rich intellectual property estate in the microRNA field. Regulus maintains its corporate headquarters in San Diego, CA.
关于雷古勒斯
Regulus Therapeutics Inc.(纳斯达克股票代码:RGLS)是一家生物制药公司,专注于发现和开发针对microRNA的创新药物。Regulus利用其寡核苷酸药物发现和开发专业知识开发了一条产品线,并辅之以microRNA领域的丰富知识产权。Regulus 的公司总部设在加利福尼亚州圣地亚哥。
Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements associated with the Company's RGLS8429 program and preclinical pipeline, the potential that RGLS8429 may be eligible for an Accelerated Approval pathway, potentially achieving therapeutic efficacy and clinical translation for patients, the expected timing for reporting interim or topline data, and the timing and future occurrence of other preclinical and clinical activities. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as "believes," "anticipates," "plans," "expects," "intends," "will," "goal," "potential" and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Regulus' current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, the risk that the approach we are taking to discover and develop drugs is novel and may never lead to marketable products, that preliminary or topline results are based on a preliminary analysis of key efficacy and safety data, and such data may change following a more comprehensive review of the data related to the clinical trial and may not be indicative of future results, the FDA has not designated RGLS8429 for an Accelerated Approval pathway and such designation may not lead to a faster development, regulatory review or approval process and does not increase the likelihood that RGLS8429 will receive marketing approval, the risk that preclinical and clinical studies may not be successful, risks related to regulatory review and approval, risks related to our reliance on third-party collaborators and other third parties, risks related to intellectual property, risks associated with the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics, the risk that additional toxicology data may be negative, and risks related to our ability to successfully secure and deploy capital. These and other risks are described in additional detail in Regulus' filings with the Securities and Exchange Commission, including under the "Risk Factors" heading of Regulus' quarterly report on Form 10-Q available on the Company's website or at www.sec.gov. All forward-looking statements contained in this press release speak only as of the date on which they were made. Regulus undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.
前瞻性陈述
本新闻稿中包含的关于非历史事实事项的陈述是 1995 年《私人证券诉讼改革法》所指的 “前瞻性陈述”,包括与公司 RGLS8429 计划和临床前产品线相关的陈述、RGLS8429 可能有资格获得加速批准途径、可能为患者实现治疗疗效和临床转化、报告中期或头条数据的预期时间以及其他发生的时间和未来发生的时间和未来发生的情况临床前和临床活动。由于此类陈述受风险和不确定性的影响,因此实际结果可能与此类前瞻性陈述所表达或暗示的结果存在重大差异。诸如 “相信”、“预期”、“计划”、“期望”、“打算”、“将”、“目标”、“潜力” 等词语以及类似的表述旨在识别前瞻性陈述。这些前瞻性陈述基于Regulus当前的预期,涉及可能永远无法实现或可能被证明不正确的假设。由于各种风险和不确定性,实际结果和事件发生时间可能与此类前瞻性陈述中的预期存在重大差异,这些风险和不确定性包括但不限于我们发现和开发药物的方法是新颖的,可能永远不会生产出可销售的产品;初步或主要结果基于对关键疗效和安全性数据的初步分析,在对临床试验相关数据进行更全面的审查之后,此类数据可能会发生变化而且可能不表示未来的结果是,美国食品药品管理局尚未将 RGLS8429 指定为加速批准途径,这种指定可能不会加快开发、监管审查或批准程序,也不会增加 RGLS8429 获得上市批准的可能性、临床前和临床研究可能不成功的风险、与监管审查和批准相关的风险、与我们依赖第三方合作者和其他第三方相关的风险、与知识产权相关的风险、与发现过程相关的风险,开发和商业化安全有效的可用作人类疗法的药物,其他毒理学数据可能为负面的风险,以及与我们成功获得和部署资金的能力相关的风险。Regulus向美国证券交易委员会提交的文件中进一步详细描述了这些风险和其他风险,包括在Regulus公司网站或www.sec.gov上发布的10-Q表季度报告的 “风险因素” 标题下。本新闻稿中包含的所有前瞻性陈述仅代表其发布之日。Regulus没有义务更新此类声明以反映在声明发表之日之后发生的事件或存在的情况。
SOURCE Regulus Therapeutics Inc.
来源 Regulus Therapeutics Inc.