CDTX Cidara Therapeutics

Cidara Therapeutics to Present New Data for Rezafungin and Influenza AVCs at the 21st ICHS Symposium

Cidara Therapeutics to Present New Data for Rezafungin and Influenza AVCs at the 21st ICHS Symposium

SAN DIEGO, Feb. 11, 2021 (GLOBE NEWSWIRE) -- Cidara Therapeutics, Inc. (Nasdaq: CDTX), a biotechnology company developing long-acting therapeutics designed to transform the standard of care for patients facing serious fungal or viral infections, today announced an oral presentation and four poster presentations at the 21st International Immunocompromised Host Society (ICHS) Symposium on Infections in the Immunocompromised Host, taking place virtually Feb. 17-19, 2021.

Cidara will share new findings related to rezafungin, its novel once-weekly echinocandin in Phase 3 trials for the treatment and prevention of serious fungal infections, in three poster presentations. Additionally, an oral overview of rezafungin by Taylor Sandison, M.D., M.P.H., chief medical officer of Cidara will be part of the symposium proceedings. Details are as follows:

Oral Presentation:

Title: Rezafungin: Evidence and Experience to Date

Presenter: Taylor Sandison, M.D., M.P.H., chief medical officer, Cidara Therapeutics

Session: Industry Symposia: New anti-fungals

Date and Time: Feb. 19, 2021 at 12:40 – 1:00 p.m. AEDT/Feb. 18, 2021 at 8:40 – 9:00 p.m. EST

Poster Presentations:

Title: Safety and Efficacy of Rezafungin in Immunocompromised Patients: Analysis of Outcomes from the Phase 2 STRIVE Trial of Rezafungin for Treatment of Candidemia and Invasive Candidiasis

Presenter: Taylor Sandison, M.D., M.P.H., chief medical officer, Cidara Therapeutics

A live Q&A session will take place on Feb. 18, 2021 at 1:00 – 2:00 p.m. AEDT/Feb. 17, 2021 at 9:00 – 10:00 p.m. EST.

Title: Efficacy and Safety by Renal Function in the Phase 2 STRIVE Trial of Rezafungin in Treatment of Candidemia and Invasive Candidiasis

Presenter: Shawn Flanagan, Ph.D., vice president clinical pharmacology & early development, Cidara Therapeutics

A live Q&A session will take place on Feb. 18, 2021 at 1:00 – 2:00 p.m. AEDT/Feb. 17, 2021 at 9:00 – 10:00 p.m. EST.

Title: Fungal Eradication with Extended Rezafungin Treatment in a Murine Model of Pneumocystis Pneumonia

Presenter: Taylor Sandison, M.D., M.P.H., chief medical officer, Cidara Therapeutics

Preclinical data from the antiviral conjugate (AVC) candidate, CD377 for prevention and treatment of influenza, will also be highlighted in one poster presentation. Details of the presentation are as follows:

Poster Presentation:

Title: Efficacy of CD377, a Novel Antiviral Fc-Conjugate, Against Influenza in a Lethal Mouse Model of Severe Combined Immunodeficiency (SCID)

Presenter: James Levin, Ph.D., senior director of preclinical development, Cidara Therapeutics

A live Q&A session will take place on Feb. 18, 2021 at 1:00 – 2:00 p.m. AEDT/Feb. 17, 2021 at 9:00 – 10:00 p.m. EST.

Copies of the abstracts will be made available on the section of the Cidara website.

About Rezafungin

Rezafungin is a novel once-weekly echinocandin being developed for both the treatment and prevention of serious fungal infections, such as candidemia and invasive candidiasis. The structure and properties of rezafungin are specifically designed to improve upon a clinically validated mechanism intended to enhance its efficacy and safety potential for patients. Cidara is currently conducting a Phase 3 clinical trial with rezafungin for the first-line treatment of candidemia and/or invasive candidiasis (ReSTORE trial) and a second Phase 3 clinical trial of once-weekly rezafungin for the prevention of invasive fungal disease in patients undergoing allogeneic blood and marrow transplantation (ReSPECT trial).

About Cloudbreak AVCs

Cidara is developing a new generation of immunotherapeutic antivirals from its Cloudbreak antiviral platform that couple potent antivirals to a human antibody fragment. These long-acting, antiviral conjugates (AVCs) directly inhibit viral proliferation while simultaneously engaging the immune system. AVCs are initially being studied for the prevention and treatment of seasonal and pandemic influenza, with the potential to deliver universal protection for an entire flu season with a single dose. Cidara is also advancing preclinical and discovery AVC programs to target other life-threatening viruses, such as RSV, HIV and CoV, including COVID-19.

About Cidara Therapeutics

Cidara is developing long-acting therapeutics designed to transform the standard of care for patients facing serious fungal or viral infections. The Company’s portfolio is comprised of its lead antifungal candidate, rezafungin, in addition to antiviral conjugates (AVCs) for the prevention and treatment of influenza and other viral diseases from Cidara’s proprietary Cloudbreak® antiviral platform. Cidara is headquartered in San Diego, California. For more information, please visit .

INVESTOR CONTACT:

Brian Ritchie

LifeSci Advisors

(212) 915-2578

MEDIA CONTACT:

Karen O’Shea, Ph.D.

LifeSci Communications

(929) 469-3860



EN
11/02/2021

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Cidara Therapeutics

 PRESS RELEASE

Cidara Therapeutics Reaches Target Enrollment of Phase 3 ANCHOR Trial ...

Cidara Therapeutics Reaches Target Enrollment of Phase 3 ANCHOR Trial Evaluating CD388 for Prevention of Seasonal Influenza in High-Risk Populations Target enrollment of 6,000 participants completed in the Northern Hemisphere Planned interim analysis in Q1 2026 will determine potential need for additional enrollment during Southern Hemisphere flu season SAN DIEGO, Nov. 24, 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 has reached ta...

 PRESS RELEASE

Cidara Therapeutics Provides Corporate Update and Reports Third Quarte...

Cidara Therapeutics Provides Corporate Update and Reports Third Quarter 2025 Financial Results Announced expanded and accelerated Phase 3 Plan for CD388, its non-vaccine influenza preventative therapeuticEnrolled and dosed first patients in Phase 3 ANCHOR study; target enrollment on track for completion in the Northern Hemisphere by December 2025; Phase 3 initiation triggered $45.0 million milestone payment to JanssenBARDA award to support expanded manufacturing and clinical development of CD388FDA granted Breakthrough Therapy designation to CD388Conference call and webcast today at 5:00 PM...

 PRESS RELEASE

Cidara Therapeutics to Participate in November Investor Conferences

Cidara Therapeutics to Participate in November Investor Conferences SAN DIEGO, Oct. 28, 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 that company management will participate in the below November investor conferences. Details are as follows: Event: Guggenheim 2nd Annual Healthcare Innovation ConferenceDate: November 11, 2025Time: 8:00 AM ETFormat: Fireside Chat Event: Jefferies London Healthcare Conference Date: November 17, 2025Time:...

 PRESS RELEASE

Cidara Therapeutics to Report Third Quarter 2025 Financial Results and...

Cidara Therapeutics to Report Third Quarter 2025 Financial Results and Host Quarterly Conference Call on November 6, 2025 SAN DIEGO, Oct. 23, 2025 (GLOBE NEWSWIRE) -- Cidara Therapeutics, Inc. (Nasdaq: CDTX), a biotechnology company using its proprietary Cloudbreak® platform to develop drug-Fc conjugate (DFC) immunotherapies, today announced that it will report its third quarter 2025 financial results and operational highlights after the close of the U.S. financial markets on Thursday, November 6, 2025. The Company will host a conference call and webcast at 5:00 PM Eastern Time to discuss...

 PRESS RELEASE

Cidara Therapeutics Announces Late-Breaking Presentation on CD388 at 1...

Cidara Therapeutics Announces Late-Breaking Presentation on CD388 at 10ᵗʰ ESWI Influenza Conference 2025 SAN DIEGO, Oct. 23, 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 gave a late-breaking presentation on its non-vaccine influenza preventative candidate, CD388, at the European Scientific Working Group on Influenza (ESWI)’s 10th Influenza Conference taking place October 20-23, 2025 in Valencia, Spain. “We are encouraged by the trans...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch