Cidara Therapeutics Unveils CD388 Phase 2 Data During ID Week 2025
Cidara Therapeutics and its Innovate Approach
Cidara Therapeutics, Inc. (NASDAQ: CDTX), a pioneering biotechnology company, is making significant strides in the development of antiviral therapies. With its proprietary Cloudbreak platform, Cidara aims to introduce revolutionary drug-Fc conjugate (DFC) therapeutics designed specifically to combat viral infections, particularly influenza. The upcoming presentation at ID Week 2025 is set to detail their latest Phase 2 clinical findings on CD388, an innovative antiviral candidate targeted against influenza A and B.
Upcoming Presentation Highlights
What to Expect
Scheduled for October 20, 2025, from 3:15 PM to 4:30 PM ET at B401-B402, Cidara's presentation will bring critical insights into the efficacy and safety of CD388. The session "Extra, Extra! New Info on Treating and Preventing RSV and Influenza" will feature Dr. James Alexander, MD, MPH, FIDSA, who will discuss the outcomes from their recent trials.
Key Features of the Clinical Trial
Study Overview
The clinical trial is characterized as a randomized, placebo-controlled study and is focused on evaluating the effectiveness of CD388 in preventing illness caused by influenza A and B among healthy, unvaccinated participants. This rigorous approach is crucial for establishing the viability of CD388 as a frontline treatment option in viral outbreaks.
About CD388 and Its Significance
CD388 represents a breakthrough in antiviral treatment strategies, as it is designed to provide long-lasting protection against both seasonal and pandemic influenza. This one-dose solution aims to directly inhibit viral proliferation, addressing critical gaps in current influenza treatment modalities. Cidara's commitment to innovation has been noted, especially since CD388 received Fast Track Designation from the FDA.
Recent Developments at Cidara Therapeutics
Progress in Clinical Trials
In June 2025, Cidara Therapeutics announced positive top-line results from its Phase 2b NAVIGATE trial. This not only reinforces the promise of CD388 but also sets the stage for the anticipated Phase 3 ANCHOR trial, which was initiated shortly after in September 2025. These developments highlight Cidara's proactive approach and determination to advance its antiviral portfolio.
Future Outlook and Company Vision
Headquartered in San Diego, California, Cidara Therapeutics is dedicated to pushing the boundaries of antiviral therapies. By harnessing its Cloudbreak platform to develop targeted therapies, the company aims to position itself as a leader in infectious disease prevention. As the global health landscape continues to evolve, Cidara seeks to address persistent challenges posed by viral infections.
Contact Information for Inquiries
Investor Contact:
Brian Ritchie
LifeSci Advisors
(212) 915-2578
britchie@lifesciadvisors.com
Media Contact:
Michael Fitzhugh
LifeSci Communications
(628) 234-3889
mfitzhugh@lifescicomms.com
Frequently Asked Questions
What is CD388?
CD388 is an antiviral candidate developed by Cidara Therapeutics aimed at preventing influenza A and B infections.
When and where will Cidara present their findings?
Cidara will present at ID Week 2025 on October 20, from 3:15 PM to 4:30 PM ET, in session B401-B402.
What is the significance of the Phase 2 trial?
The Phase 2 trial evaluates the safety and efficacy of CD388 in healthy, unvaccinated participants, providing crucial data for future trials.
What recent progress has Cidara made?
Cidara reported positive results from its Phase 2b NAVIGATE trial in June 2025 and initiated the Phase 3 ANCHOR trial in September 2025.
How can I contact Cidara Therapeutics for more information?
For inquiries, you can reach Brian Ritchie at LifeSci Advisors at (212) 915-2578 or by email at britchie@lifesciadvisors.com.
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