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Cidara Therapeutics Provides Corporate Update and Reports First Quarter 2023 Financial Results
5/11/2023
Cidara Therapeutics, Inc. (NASDAQ: CDTX) today reported financial results for the first quarter ended March 31, 2023 and provided an update on its corporate activities and product pipeline.
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Cidara Therapeutics Presents New Preclinical Data on Novel Drug-Fc Conjugate CD388 at the 7th International Society for Influenza and Other Respiratory Virus Diseases Conference
5/3/2023
Cidara Therapeutics, Inc. is delivering two oral presentations highlighting new preclinical data on its novel drug-Fc conjugate (DFC) candidate targeting influenza A and B, CD388, at the 7th International Society for Influenza and Other Respiratory Virus Diseases (ISIRV) conference.
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Cidara Therapeutics Receives $20 Million Milestone Payment Following FDA Approval of REZZAYO™
4/24/2023
Cidara Therapeutics, Inc. today announced receipt of a $20 million milestone payment from Melinta Therapeutics following the U.S. Food and Drug Administration (FDA) approval of REZZAYO™ (rezafungin for injection), a novel, once-weekly echinocandin antifungal approved for the treatment of candidemia and invasive candidiasis.
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Cidara Therapeutics to Participate in Upcoming March 2023 Investor Conferences
3/31/2023
Cidara Therapeutics, Inc. announced that Jeffrey Stein, Ph.D., President and Chief Executive Officer, is scheduled to participate in the following upcoming investor conferences.
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Wednesday, the FDA approved Cidara Therapeutics and Melinta Therapeutics’ Rezzayo (rezafungin) injection to treat candidemia and invasive candidiasis.
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Cidara Therapeutics Provides Corporate Update and Reports Fourth Quarter and Full Year 2022 Financial Results
3/23/2023
Cidara Therapeutics, Inc. today reported financial results for the three months and full year ended December 31, 2022 and provided an update on its corporate activities and product pipeline.
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Cidara Therapeutics and Melinta Therapeutics Announce FDA Approval of REZZAYO™ (rezafungin for injection) for the Treatment of Candidemia and Invasive Candidiasis
3/22/2023
Cidara Therapeutics, Inc. (Nasdaq: CDTX) and Melinta Therapeutics, LLC today announced that the U.S. Food and Drug Administration (FDA) approved REZZAYO™ (rezafungin for injection) for the treatment of candidemia and invasive candidiasis in adults with limited or no alternative treatment options.
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An advisory committee will meet March 22 to discuss the fate of Biogen and Ionis’ ALS hopeful tofersen. For that and more, see inside.
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Cidara Therapeutics Presents Preclinical Data on CD73-Targeting Drug-Fc Conjugate at the 2023 ESMO Targeted Anticancer Therapies Congress
3/7/2023
Cidara Therapeutics, Inc. presented preclinical data on a CD73-targeting drug-Fc conjugate (DFC) candidate, CBO-212, from the Company’s Cloudbreak ® platform, at the ESMO Targeted Anticancer Therapies Congress (ESMO TAT) in Paris, March 6-8, 2023.
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Cidara Therapeutics Announces Closing of Public Offerings of Common Stock and Preferred Stock and Full Exercise of Underwriter’s Option to Purchase Additional Shares in Public Offering of Common Stock
3/7/2023
Cidara Therapeutics, Inc. today announced the closing of its previously announced concurrent but separate underwritten public offerings of 11,086,000 shares of its common stock, including the exercise in full by the underwriter of its option to purchase an additional 1,446,000 shares of common stock.
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Cidara Therapeutics Announces Pricing of Public Offerings of Common Stock and Preferred Stock
3/3/2023
Cidara Therapeutics, Inc. today announced the pricing of concurrent but separate underwritten public offerings of 9,640,000 shares of its common stock and 286,000 shares.
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Cidara Therapeutics Announces Underwritten Public Offerings of Common Stock and Preferred Stock
3/2/2023
Cidara Therapeutics, Inc. announced concurrent but separate underwritten public offerings of its common stock and its Series X Convertible Preferred Stock.
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Cidara Therapeutics Announces Promising Interim Phase 2a Data Assessing the Safety and Efficacy of a Single Dose of CD388 in an Influenza Challenge Model
3/1/2023
Cidara Therapeutics, Inc. today announced promising efficacy and safety data from a planned interim analysis of the ongoing Phase 2a trial evaluating the pre-exposure prophylactic activity of CD388 against the H3N2 influenza A virus strain, as of a February 13, 2023 data cut-off.
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Cidara to Present at ESMO Targeted Anticancer Therapies Congress
2/28/2023
Cidara Therapeutics, Inc. today announced that it will present highlights from pharmacokinetic studies of a CD73-targeting drug-Fc conjugate (DFC) oncology candidate from the Company’s Cloudbreak ® platform at the ESMO Targeted Anticancer Therapies Congress (ESMO TAT) in Paris, March 6-8, 2023.
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Cidara Therapeutics Regains Compliance with Nasdaq Minimum Bid Price Requirement - February 14, 2023
2/14/2023
Cidara Therapeutics, Inc., a biotechnology company developing long-acting therapeutics designed to help improve the standard of care for patients facing serious diseases, announced that it has received formal notice from The Nasdaq Stock Market, LLC, stating that the Company has regained compliance with the minimum bid price requirement set forth in Nasdaq Listing Rule 5550.
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Cidara Therapeutics and WuXi XDC Expand Collaboration for IND-enabling CMC Development to Advance Cidara’s CD73 Oncology DFC Program
2/1/2023
Cidara Therapeutics, Inc. and WuXi XDC announced an expansion of their existing collaboration under which WuXi XDC will provide investigational new drug -enabling chemistry, manufacturing and controls development services for Cidara’s CD73 oncology DFC program.
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Cidara Therapeutics and Melinta Therapeutics Announce FDA Advisory Committee Recommends Approval of Rezafungin for the Treatment of Candidemia and Invasive Candidiasis
1/25/2023
Cidara Therapeutics, Inc. (Nasdaq: CDTX) and Melinta Therapeutics, LLC today announced that the U.S. Food and Drug Administration (FDA) Antimicrobial Drugs Advisory Committee voted favorably 14 to 1 that Cidara, as part of its New Drug Application (NDA).
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Cidara Therapeutics Nominates First Oncology Clinical Development Candidate from its Cloudbreak® PlatformCBO-212 is a first-in-class inhibitor of CD73 cancer immunotherapy target
1/4/2023
Cidara Therapeutics, Inc. (NASDAQ: CDTX), a biotechnology company developing long-acting therapeutics designed to improve the standard of care for patients facing serious diseases, today announced that it has selected its first oncology drug-Fc conjugate (DFC) candidate from the company’s Cloudbreak® platform: CBO-212, targeting CD73.
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Paratek Pharmaceuticals Appoints Jeffrey Stein as Lead Independent Director of the Board
12/20/2022
Paratek Pharmaceuticals, Inc. (NASDAQ:PRTK) today announced that the Company’s independent directors of the Board have appointed Jeffrey Stein, PhD as its first Lead Independent Director, effective December 8, 2022.
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Cidara Therapeutics Announces Issuance of First U.S. Patent for CD388Initial CD388 clinical data expected in the first half of 2023
12/1/2022
Cidara Therapeutics, Inc. (NASDAQ: CDTX) today announced that the U.S. Patent and Trademark Office issued U.S. Patent No. 11,510,992, entitled Compositions and Methods for the Treatment of Viral Infections, for CD388, a highly potent, long-acting drug-Fc conjugate (DFC) designed to achieve universal prevention of seasonal and pandemic influenza.