Cidara Therapeutics

Cidara Therapeutics

Cidara Therapeutics is developing innovative therapies.

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$350m

Post IPO Equity
Total Funding000k

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Revenues, earnings & profits over time
USD2021202220232024202520262027
Revenues0000000000000000000000000000
% growth311 %30 %(1 %)(98 %)--20 %
EBITDA0000000000000000000000000000
% EBITDA margin(85 %)(46 %)(38 %)(13794 %)-(4120 %)(3816 %)
Profit0000000000000000000000000000
% profit margin(86 %)(46 %)(36 %)(13320 %)-(4784 %)(4153 %)
EV0000000000000000000000000000
EV / revenue00.0x00.0x00.0x00.0x00.0x00.0x00.0x
EV / EBITDA00.0x00.0x00.0x00.0x00.0x00.0x00.0x
R&D budget0000000000000000000000000000
R&D % of revenue147 %117 %107 %12295 %---

Source: Company filings or news article, Equity research estimates

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More about Cidara Therapeutics
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Cidara Therapeutics, established in 2012 by a team including Kevin Forrest, Ph.D., H. Shaw Warren, M.D., and Dirk Thye, M.D., is a clinical-stage biotechnology firm concentrated on developing long-acting therapeutics for patients with severe diseases. The company's strategic focus is on its proprietary Cloudbreak® platform, which is engineered to create drug-Fc conjugates (DFCs). These DFCs are designed to provide both prevention and treatment for life-threatening illnesses by engaging the immune system. The company went public with an initial public offering in April 2015, a significant milestone that provided capital for its research and development programs.

The core of Cidara's business revolves around leveraging its DFC technology to create a new generation of immunotherapies. The Cloudbreak platform facilitates the development of conjugates that can be administered infrequently, aiming to improve patient adherence and outcomes. This approach targets a market where long-acting, effective treatments are critical, particularly for vulnerable patient populations. Cidara's primary product candidate is Rezafungin (rezafungin for injection), a novel, once-weekly echinocandin being developed for the treatment and prevention of serious fungal infections like candidemia and invasive candidiasis. In 2023, the FDA approved Rezafungin, now marketed as REZZAYO™, for the treatment of candidemia and invasive candidiasis in adult patients with limited or no alternative treatment options. This approval marked a major achievement for the company.

Cidara's business model is centered on research, development, and strategic collaborations for the commercialization of its product candidates. The company generates revenue through partnership agreements, which include upfront payments, milestone payments, and potential royalties on sales. A key partnership is the exclusive license agreement with Melinta Therapeutics for the commercialization of REZZAYO™ in the United States. For markets outside the U.S., Cidara has established agreements with other pharmaceutical companies, such as Mundipharma, to handle commercialization, allowing Cidara to focus on its core competency of drug development. The company is also advancing its pipeline to include treatments for oncology, underscoring its commitment to addressing unmet medical needs across different therapeutic areas.

Keywords: biotechnology, drug-Fc conjugate, immunotherapy, infectious diseases, oncology, Cloudbreak platform, Rezafungin, REZZAYO, long-acting therapeutics, clinical-stage

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