Cidara Therapeutics to Participate in Evercore 7th Annual HealthCONx Conference
Cidara Therapeutics to Participate in Evercore 7th Annual HealthCONx Conference
SAN DIEGO, Nov. 19, 2024 — Cidara Therapeutics, Inc. (Nasdaq: CDTX), a biotechnology company using its proprietary Cloudbreak platform to develop drug-Fc conjugate (DFC) immunotherapies designed to save lives and improve the standard of care for patients facing serious diseases, today announced that Jeffrey Stein, Ph.D., President and Chief Executive Officer, will participate in the Evercore 7th Annual HealthCONx Conference.
圣地亚哥,2024年11月19日——利用其专有的Cloudbreak平台开发药物-FC偶联物(DFC)免疫疗法的生物技术公司(纳斯达克股票代码:CDTX)今天宣布,总裁兼首席执行官杰弗里·斯坦博士将参加Evercore第七届年度HealthConx会议。
Details are as follows:
详情如下:
Event: Evercore 7th Annual HealthCONx Conference
Date: Tuesday, December 3, 2024
Time: 7:55 AM ET
Format: Fireside chat
Webcast:
活动:Evercore 第七届年度 HealthConx 会议
日期:2024 年 12 月 3 日星期二
时间:美国东部时间上午 7:55
格式:炉边聊天
网络直播:
A replay of the presentation will be available in the Investors section on the Company's website at . The replay of the presentation will be available for 90 days.
该演讲的重播将在公司网站的 “投资者” 栏目中公布,网址为。演示的重播将持续90天。
Cidara will also participate in one-on-one investor meetings during this event. Investors interested in meeting with Cidara at the conference should contact their Evercore representative directly.
在本次活动期间,Cidara还将参加一对一的投资者会议。有兴趣在会议上与Cidara会面的投资者应直接联系其Evercore代表。
About Cidara Therapeutics
Cidara Therapeutics is using its proprietary Cloudbreak platform to develop novel drug-Fc conjugates (DFCs) comprising targeted small molecules or peptides coupled to a proprietary human antibody fragment (Fc). Cidara's lead DFC candidate, CD388, is a long-acting antiviral designed to achieve universal prevention of seasonal and pandemic influenza with a single dose by directly inhibiting viral proliferation. In June 2023, CD388 was granted Fast Track Designation by the U.S. Food and Drug Administration (FDA), and the Company announced initiation of a Phase 2b trial in September 2024. Additional DFCs have been developed for oncology and in July 2024 Cidara received IND clearance for CBO421 which is intended to target CD73 in solid tumors. Cidara is headquartered in San Diego, California. For more information, please visit .
关于 Cidara Therapeu
Cidara Therapeutics正在使用其专有的Cloudbreak平台开发新的药物-Fc偶联物(DFC),该偶联物包括靶向小分子或与专有的人类抗体片段(Fc)耦合的肽。Cidara的主要DFC候选药物 CD388 是一种长效抗病毒药物,旨在通过直接抑制病毒增殖,以单剂量实现季节性和大流行性流感的普遍预防。2023 年 6 月,CD388 被美国食品药品监督管理局 (FDA) 授予 “快速通道” 称号,该公司于 2024 年 9 月宣布启动 20期试验。已经开发了更多用于肿瘤学的 DFC,2024 年 7 月,Cidara 获得了 CBO421 的临床许可,该药物旨在靶向实体瘤中的 CD73。Cidara 总部位于加利福尼亚州圣地亚哥。欲了解更多信息,请访问。
INVESTOR CONTACT:
Brian Ritchie
LifeSci Advisors
(212) 915-2578
britchie@lifesciadvisors.com
投资者联系人:
布莱恩·里奇
生命科学顾问
(212) 915-2578
britchie@lifesciadvisors.com
MEDIA CONTACT:
Michael Fitzhugh
LifeSci Communications
mfitzhugh@lifescicomms.com
媒体联系人:
迈克尔·菲茨休
LifeSci
mfitzhugh@lifescicomms.com