{"id":57428,"date":"2024-07-19T12:04:01","date_gmt":"2024-07-19T12:04:01","guid":{"rendered":"https:\/\/english.saigonbiz.com.vn\/2024\/07\/19\/dare-bioscience-regains-compliance-with-nasdaq-minimum-bid-price-rule\/"},"modified":"2024-07-19T12:04:01","modified_gmt":"2024-07-19T12:04:01","slug":"dare-bioscience-regains-compliance-with-nasdaq-minimum-bid-price-rule","status":"publish","type":"post","link":"https:\/\/english.saigonbiz.com\/vn\/dare-bioscience-regains-compliance-with-nasdaq-minimum-bid-price-rule\/","title":{"rendered":"Dar\u00e9 Bioscience Regains Compliance with Nasdaq Minimum Bid Price Rule"},"content":{"rendered":"<div>\n<p align=\"left\">SAN DIEGO, July  19, 2024  (GLOBE NEWSWIRE) &#8212; Dare\u0301\u00a0Bioscience, Inc.\u00a0(NASDAQ: DARE), a leader in innovation for the health and wellbeing of women, announced that it was notified by the Nasdaq Office of General Counsel that the Company regained compliance with the minimum bid price requirement in Nasdaq Listing Rule 5550(a)(2) as a result of the closing bid price of the Company\u2019s common stock being $1.00 per share or greater for 10 consecutive trading sessions and that the matter is closed.<\/p>\n<p>\u201cWe are thrilled to announce that we have regained compliance with the Nasdaq minimum bid price rule,\u201d said Sabrina Martucci Johnson, President and CEO of Dar\u00e9 Bioscience. \u201cThis strengthens our position in the market and enhances our ability to drive our vision forward. We look forward to the opportunity to accelerate our development efforts on key programs in our portfolio and to ultimately provide great therapeutic options for women.\u201d<\/p>\n<p>\u201cWe continue to enroll participants in our pivotal Phase 3 study of Ovaprene<sup>\u00ae<\/sup>, our potentially first-in-category hormone-free monthly intravaginal contraceptive candidate, at sites across the U.S.,\u201d Johnson continued. \u201cWe are also continuing activities to support progressing toward a Phase 3 trial of Sildenafil Cream, 3.6% in female sexual arousal disorder, for which there are currently no FDA-approved treatments. We continue to execute on our mission to accelerate development of and bring to market innovative treatments that women want and need by advancing our late-stage candidates \u2013 all of which represent a first-in-category opportunity \u2013 as we seek to deliver value for all Dar\u00e9 stakeholders.\u201d<\/p>\n<p><strong>About Dar\u00e9 Bioscience<\/strong><br \/>Dar\u00e9 Bioscience is a biopharmaceutical company committed to advancing innovative products for women\u2019s health. The company\u2019s mission is to identify, develop and bring to market a diverse portfolio of differentiated therapies that prioritize women&#8217;s health and well-being, expand treatment options, and improve outcomes, primarily in the areas of contraception, vaginal health, reproductive health, menopause, sexual health and fertility.<\/p>\n<p>The first FDA-approved product to emerge from Dar\u00e9\u2019s portfolio of women\u2019s health product candidates is XACIATO&#x2122; (clindamycin phosphate) vaginal gel 2%, a lincosamide antibacterial indicated for the treatment of bacterial vaginosis in female patients 12 years of age and older, which is under a global license agreement with Organon. Organon commenced\u00a0U.S.\u00a0marketing of XACIATO in the fourth quarter of 2023. Dar\u00e9\u2019s portfolio also includes potential first-in-category candidates in clinical development: Ovaprene<sup>\u00ae<\/sup>, a novel, hormone-free monthly intravaginal contraceptive whose\u00a0U.S.\u00a0commercial rights are under a license agreement with Bayer; Sildenafil Cream, 3.6%, a novel cream formulation of sildenafil, the active ingredient in Viagra<sup>\u00ae<\/sup>, to treat female sexual arousal disorder (FSAD); and DARE-HRT1, a combination bio-identical estradiol and progesterone intravaginal ring for menopausal hormone therapy. To learn more about XACIATO, Dar\u00e9\u2019s full portfolio of women\u2019s health product candidates, and Dar\u00e9\u2019s mission to deliver differentiated therapies for women, please visit\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=eT8HASeSdS4NP34FtM4ffEDWIDRbyDXANHeVZDcI6Ci9vITBDf4vinjslwNpWkl2vTrk9xCpUGdEPssuBIeL37DKs0FzNggDWIDTsr1VZYI=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"www.darebioscience.com\">www.darebioscience.com<\/a>.<\/p>\n<p>Dar\u00e9 Bioscience leadership has been named on the Medicine Maker\u2019s Power List and Endpoints News\u2019 Women in Biopharma 2022. In 2023, Dar\u00e9&#8217;s CEO was honored as one of Fierce Pharma\u2019s Most Influential People in Biopharma for Dar\u00e9\u2019s contributions to innovation and advocacy in the women\u2019s health space. Dar\u00e9 Bioscience placed #1 in the\u00a0Small Company\u00a0category of the San Diego Business Journal\u2019s 2023 Best Places to Work Awards.<\/p>\n<p>Dar\u00e9 may announce material information about its finances, product and product candidates, clinical trials and other matters using the Investors section of its website (<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=G6eZfL_NlHGWEN05PMqy5igyx2WjGdWulTRqvxDq-ciTwxNIbaFkTOPf-nubky1qXoytlj4xO7GUWtVRQzkskEjt6DU-RwzgqlIeD0Qh0vM=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\">http:\/\/ir.darebioscience.com<\/a>),\u00a0SEC\u00a0filings, press releases, public conference calls and webcasts. Dar\u00e9 will use these channels to distribute material information about the company and may also use social media to communicate important information about the company, its finances, product and product candidates, clinical trials and other matters. The information Dar\u00e9 posts on its investor relations website or through social media channels may be deemed to be material information. Dar\u00e9 encourages investors, the media, and others interested in the company to review the information Dar\u00e9 posts in the Investors section of its website and to follow these X\u00a0(formerly Twitter) accounts: @SabrinaDareCEO and @DareBioscience. Any updates to the list of social media channels the company may use to communicate information will be posted in the Investors section of Dar\u00e9\u2019s website.<\/p>\n<p><strong>Forward-Looking Statements<\/strong><br \/><em>Dar\u00e9 cautions you that all statements, other than statements of historical facts, contained in this press release, are forward-looking statements. Forward-looking statements, in some cases, can be identified by terms such as \u201cbelieve,\u201d \u201cmay,\u201d \u201cwill,\u201d \u201cestimate,\u201d \u201ccontinue,\u201d \u201canticipate,\u201d \u201cdesign,\u201d \u201cintend,\u201d \u201cexpect,\u201d \u201ccould,\u201d \u201cplan,\u201d \u201cpotential,\u201d \u201cpredict,\u201d \u201cseek,\u201d \u201cshould,\u201d \u201cwould,\u201d \u201ccontemplate,\u201d \u201cproject,\u201d \u201ctarget,\u201d \u201cobjective,\u201d or the negative version of these words and similar expressions. In this press release, forward-looking statements include, but are not limited to, statements relating to plans and expectations with respect to Dar\u00e9\u2019s product candidates, including clinical development plans, targeted indications, the potential for FDA approval of Ovaprene based on a single pivotal clinical study, and the expectation that a product candidate could be a first-in-category product. As used in this press release, the description of a product candidate as \u201cfirst-in-category\u201d is a forward-looking statement relating to the potential of the candidate to represent a new category of product if it were to receive marketing approval for the indication for which Dar\u00e9 is developing it. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause Dar\u00e9\u2019s actual results, performance or achievements to be materially different from future results, performance or achievements expressed or implied by the forward-looking statements in this press release, including, without limitation, risks and uncertainties related to: Dar\u00e9\u2019s ability to raise additional capital when and as needed to advance its product candidates, execute its business strategy and continue as a going concern; Dar\u00e9\u2019s ability to develop, obtain FDA or foreign regulatory approval for, and commercialize its product candidates and to do so on communicated timelines; failure or delay in starting, conducting and completing clinical trials of a product candidate; Dar\u00e9\u2019s ability to design and conduct successful clinical trials, to enroll a sufficient number of patients, to meet established clinical endpoints, to avoid undesirable side effects and other safety concerns, and to demonstrate sufficient safety and efficacy of its product candidates; Dar\u00e9\u2019s dependence on third parties to conduct clinical trials and manufacture and supply clinical trial material and commercial product; the risk that positive findings in early clinical and\/or nonclinical studies of a product candidate may not be predictive of success in subsequent clinical and\/or nonclinical studies of that candidate; the risk that the FDA, other regulatory authorities, members of the scientific or medical communities or investors may not accept or agree with Dar\u00e9\u2019s interpretation of or conclusions regarding data from clinical studies of its product candidates; the risk that development of a product candidate requires more clinical or nonclinical studies than Dar\u00e9 anticipates; the loss of, or inability to attract, key personnel; the effects of macroeconomic conditions, geopolitical events, public health emergencies, and major disruptions in government operations on Dar\u00e9\u2019s operations, financial results and condition, and ability to achieve current plans and objectives; the risk that developments by competitors make Dar\u00e9\u2019s product or product candidates less competitive or obsolete; difficulties establishing and sustaining relationships with development and\/or commercial collaborators; failure of Dar\u00e9\u2019s product or product candidates, if approved, to gain market acceptance or obtain adequate coverage or reimbursement from third-party payers; Dar\u00e9\u2019s ability to retain its licensed rights to develop and commercialize a product or product candidate; Dar\u00e9\u2019s ability to satisfy the monetary obligations and other requirements in connection with its exclusive, in-license agreements covering the critical patents and related intellectual property related to its product and product candidates; Dar\u00e9\u2019s ability to adequately protect or enforce its, or its licensor\u2019s, intellectual property rights; the lack of patent protection for the active ingredients in certain of Dar\u00e9\u2019s product candidates which could expose its products to competition from other formulations using the same active ingredients; product liability claims; governmental investigations or actions relating to Dar\u00e9\u2019s product or product candidates or the business activities of Dar\u00e9, its commercial collaborators or other third parties on which Dar\u00e9 relies; the impact of pharmaceutical industry regulation and health care legislation in the United States and internationally; global trends toward health care cost containment; cybersecurity incidents or similar events that compromise Dar\u00e9\u2019s technology systems or those of third parties on which it relies and\/or significantly disrupt Dar\u00e9\u2019s business; and disputes or other developments concerning Dar\u00e9\u2019s intellectual property rights. Dar\u00e9\u2019s forward-looking statements are based upon its current expectations and involve assumptions that may never materialize or may prove to be incorrect. All forward-looking statements are expressly qualified in their entirety by these cautionary statements. For a detailed description of Dar\u00e9\u2019s risks and uncertainties, you are encouraged to review its documents filed with the SEC including Dar\u00e9\u2019s recent filings on Form 8-K, Form 10-K and Form 10-Q. You are cautioned not to place undue reliance on forward-looking statements, which speak only as of the date on which they were made. Dar\u00e9 undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.<\/em><\/p>\n<p><strong>Contacts:<\/strong><\/p>\n<p><strong>Media and Investors on behalf of Dar\u00e9\u00a0Bioscience, Inc:<\/strong><\/p>\n<p>Camilla White\u00a0\/ Simona Kormanikova<br \/>Dentons Global Advisors<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=VAFEpFYB-pOmkUGQWXrnzje_C6Endao2yZKSuKXRe5MEtnOG6fSa81A--pv-QlxOaII_NjU1dLBh-Vr1xZ7p4ltr09wv25TuMe9KX_XnvBy9gucbYjdjtQao45wHDJDm-I9kUwdz1ehNt0fdCTm5FQ==\" rel=\"nofollow noopener\" target=\"_blank\" title=\"DareBioscience@dentonsglobaladvisors.com\">DareBioscience@dentonsglobaladvisors.com<\/a>\u00a0\/ 1.212.466.6450<\/p>\n<p>Source: Dar\u00e9\u00a0Bioscience, Inc.<\/p>\n<p><img decoding=\"async\" src=\"https:\/\/ml.globenewswire.com\/media\/OGMxZGQ4ZjItYTFkMi00MGNiLThhYjctZGRiZjU4ZWQ2OWI1LTEwMTk5Mzc=\/tiny\/Dar-Bioscience-Inc-.png\" referrerpolicy=\"no-referrer-when-downgrade\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>SAN DIEGO, July 19, 2024 (GLOBE NEWSWIRE) &#8212; Dare\u0301\u00a0Bioscience, Inc.\u00a0(NASDAQ: DARE), a leader in innovation for the health and wellbeing of women, announced that it was notified by the Nasdaq Office of General Counsel that the Company regained compliance with the minimum bid price requirement in Nasdaq Listing Rule 5550(a)(2) as a result of the [&#8230;]\n","protected":false},"author":1,"featured_media":57429,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-57428","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-pr-newswire"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v21.6 (Yoast SEO v21.6) - 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