SAN DIEGO, Oct. 02, 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 received an award valued up to $339M from the Biomedical Advanced Research and Development Authority (BARDA), part of the Administration for Strategic Preparedness and Response (ASPR) within the U.S. Department of Health and Human Services (HHS). The multi-year agreement consists of a ...

We recently compiled a list of the 12 Best Performing Healthcare Stocks to Buy Right Now. Cidara Therapeutics, Inc. is one of them. Cidara Therapeutics, Inc. (NASDAQ:CDTX) is a biotechnology company leveraging its proprietary Cloudbreak® platform to develop drug-Fc conjugate (DFC) therapeutics. Its lead candidate, CD388, is a long-acting antiviral designed to provide universal prevention of seasonal and pandemic influenza with a single dose by directly inhibiting viral replication. In September 2025, CDT ...

Key Points The biotech launched a late-stage trial of a non-vaccine flu preventative. There is a vast addressable market for such a product. 10 stocks we like better than Cidara Therapeutics › Cidara Therapeutics (NASDAQ: CDTX) had some encouraging news to deliver at the end of the trading week, and investors traded the biotech's stock up as a result. It closed Friday nearly 7% higher in price, easily outpacing the 0.6% increase of the bellwether S&P 500 index. Phase 3 trial begins for investigatio ...

Key Takeaways Cidara shares have jumped 217.8% in 2025 so far on progress with its influenza drug candidate CD388.The phase IIb NAVIGATE study met all primary and secondary endpoints across multiple dose levels.The phase III ANCHOR study began ahead of schedule and could support regulatory filing if successful.Shares of Cidara Therapeutics (CDTX) have skyrocketed 217.8% in the year so far, driven by positive updates from the development program of its only clinical-stage pipeline candidate, CD388, for the p ...

- Phase 3 study expected to enroll 6,000 participants starting in the Northern Hemisphere - Participants will include adults over 65 years of age in addition to individuals with high-risk co-morbidities and immune compromised status SAN DIEGO, Sept. 25, 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 the first participants have been dosed in its Phase 3 ...

The trial will now include a broader population, such as adults over 65, individuals with high-risk co- morbidities, and those with compromised immune systems. This expansion aims to demonstrate the drug's effectiveness across diverse groups, potentially increasing its market appeal. Currently, CDTX is priced at $88.58, reflecting a 20.53% increase, or $15.09 rise. The stock has fluctuated between $77 and $90.64 today, with the latter being its highest price in the past year. CDTX has a market cap of $2.25 ...

"Successful investing takes time, discipline, and patience. No matter how great the talent or effort, some things just take time", said Warren Buffett. The question now is - did you have the patience to hold on to stocks we highlighted and reap the gains? Cidara Therapeutics Inc. (CDTX) touched a 52-week high of $87.19 today, as it continues to progress with its accelerated development plan for CD388, a non-vaccine preventive treatment for seasonal influenza. The company will be pursuing a Biologics Licens ...

Cidara Therapeutics (NASDAQ:CDTX) added ~15% on Wednesday after the biotech announced an accelerated timeline for a Phase 3 registrational trial designed to evaluate its experimental flu therapy CD388. The update followed an End-of-Phase 2 meeting the company conducted with the ...

BILL O'NEIL ARCHIVES: Analysis Of The Greatest Stocks Of All Time Shares of Cidara Therapeutics (CDTX), which have already rocketed more than 173% this year, surged to a five-year high Wednesday on plans to expand testing for its non-vaccine flu prevention drug. Following a meeting with the Food and Drug Administration, Cidara accelerated plans to start Phase 3 testing by six months. The company's goal is to time out its testing with the flu season in the Northern Hemisphere. The agency also encouraged the ...

Core Insights - Cidara Therapeutics is advancing its Phase 3 trial for CD388 following FDA feedback, expanding the study population to include adults over 65 years and increasing the potential patient pool from approximately 50 million to over 100 million in the U.S. [1][2][3] Group 1: Phase 3 Study Details - The Phase 3 study will be a global, multicenter, randomized, double-blind, placebo-controlled trial evaluating a single 450-milligram dose of CD388 administered subcutaneously at the start of the flu season [2][3] - Enrollment is set to begin by the end of September 2025 in the Northern Hemisphere, with a target of 6,000 subjects, representing a six-month acceleration from the previous timeline [2][6] - An interim analysis will be conducted after the Northern Hemisphere flu season to assess trial size and enrollment for the Southern Hemisphere [2][3] Group 2: Company Background and Product Information - Cidara Therapeutics utilizes its proprietary Cloudbreak® platform to develop drug-Fc conjugate (DFC) therapeutics, with CD388 being a long-acting antiviral aimed at universal prevention of influenza [4] - CD388 received Fast Track Designation from the FDA in June 2023, and positive results from the Phase 2b NAVIGATE trial were announced in June 2025 [4] - The company is also developing additional DFCs for oncology, including CBO421, which targets CD73 in solid tumors [4]