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Cidara Therapeutics to Present at 10th ESWI Influenza Conference 2025

Key Takeaway: Cidara Therapeutics announced a late-breaking presentation at the 10th ESWI Influenza Conference in Valencia, Spain, scheduled for October 20-23, 2025. The presentation will focus on the translational efficacy of CD388, a novel Drug Fc-Conjugate, in mouse influenza infection models. This follows positive results from the Phase 2b NAVIGATE clinical study, and CD388 has been granted Fast Track Designation by the FDA.

Market Sentiment Analysis

POSITIVE FACTORS

  • Cidara Therapeutics will present at a prominent influenza conference.
  • The presentation will highlight positive results from the Phase 2b NAVIGATE trial.
  • CD388 has received Fast Track Designation from the FDA.

Full Press Release Details

SAN DIEGO, Oct. 10, 2025 (GLOBE NEWSWIRE) -- Cidara Therapeutics, Inc. (Nasdaq: CDTX), a biotechnology company using its proprietary Cloudbreak®platform to develop drug-Fc conjugate (DFC) therapeutics, today announced it will have a late-breaking presentation at the European Scientific Working Group on Influenza (ESWI)’s 10th Influenza Conference taking place October 20-23, 2025 in Valencia, Spain.

Presentation details are summarized below:

Late-Breaking Abstract Title:Translational efficacy of CD388, a novel Drug Fc-Conjugate (DFC), in mouse influenza infection models: application to prevention efficacy in the recently completed Ph2b NAVIGATE clinical study.

Presenter:Voon Ong, Ph.D.

Session:Late Breakers: Novel and Outstanding Discoveries

Session Date and Time:Thursday, October 23, 2025, 2:00-3:30 pm CET

About Cidara TherapeuticsCidara Therapeutics is using its proprietary Cloudbreak®platform to develop novel DFCs comprising targeted small molecules or peptides coupled to a proprietary human antibody fragment. 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 FDA. Cidaraannouncedpositive top-line results from its Phase 2b NAVIGATE trial in June 2025 andinitiatedits Phase 3 ANCHOR trial in September 2025. Cidara is headquartered in San Diego, California. For more information, please visitwww.cidara.com.

INVESTOR CONTACT:Brian RitchieLifeSci Advisors(212) 915-2578britchie@lifesciadvisors.com

MEDIA CONTACT:Michael FitzhughLifeSci Communications(628) 234-3889mfitzhugh@lifescicomms.com

Frequently Asked Questions

What is the focus of Cidara's presentation at the ESWI Conference?

Cidara's presentation will focus on the translational efficacy of CD388 in influenza models.

When is the ESWI Influenza Conference taking place?

The ESWI Influenza Conference is scheduled for October 20-23, 2025.

What designation has CD388 received from the FDA?

CD388 has been granted Fast Track Designation by the FDA.

Who will present at the ESWI Conference?

Dr. Voon Ong will present at the conference.

What are the results from the Phase 2b NAVIGATE trial?

Cidara announced positive top-line results from the Phase 2b NAVIGATE trial in June 2025.

Last updated: Oct 10, 2025