Daré Bioscience, Inc. (NASDAQ: DARE), a leader in women’s
health innovation, today announced the completion of its registered
direct offering of common stock and warrants to purchase common
stock priced at-the-market under Nasdaq rules with an institutional
investor and an investor affiliated with the licensor of one of the
company’s early stage product candidates. The aggregate gross
proceeds to Daré, before deducting offering expenses payable by
Daré, were $7.0 million. The closing occurred on September 1, 2023.
“This financing strengthened our balance sheet,
providing cash to help us deliver on important portfolio milestones
this year,” said Sabrina Martucci Johnson, President and CEO of
Daré Bioscience. “In addition to the commercial launch of XACIATO
in the U.S. by Organon, we are looking forward to the commencement
of patient enrollment in our pivotal Phase 3 clinical study of
Ovaprene, our investigational, hormone-free, monthly intravaginal
contraceptive, and topline data from our Phase 1 clinical study of
DARE-PDM1, an investigational proprietary hydrogel formulation of
diclofenac we are developing as a vaginally administered treatment
for primary dysmenorrhea, more commonly referred to as menstrual
cramps and pain,” continued Ms. Johnson. “We also look forward to
an end-of-Phase-2 meeting, targeted for 2023, with the FDA for our
Sildenafil Cream, 3.6% program, to support Phase 3 commencement in
early 2024; our investigational formulation of sildenafil is
designed to treat female sexual arousal disorder and/or female
sexual interest/arousal disorder utilizing the active ingredient in
Viagra®. In addition, we are pleased to announce that we previously
entered into a license agreement with Douglas Pharmaceuticals, a
New Zealand based pharmaceutical company, under which we acquired
exclusive rights to develop and commercialize in the United States
an investigational, novel proprietary lopinavir and ritonavir
combination soft gel vaginal insert for the treatment of cervical
intraepithelial neoplasia, also known as cervical dysplasia. There
is no FDA-approved pharmaceutical treatment for cervical dysplasia,
a precancerous condition in women strongly linked to HPV infection,
the most common sexually transmitted infection in the U.S. Current
surgical procedures to treat cervical dysplasia are invasive and
can adversely impact future pregnancies. A pharmaceutical approach
could provide women with an important alternative to surgery to
treat this condition.”
Daré’s completed equity financing included
minority participation by an investor affiliated with Douglas.
About Daré Bioscience
Daré Bioscience is a biopharmaceutical company
committed to advancing innovative products for women’s health. The
company’s mission is to identify, develop and bring to market a
diverse portfolio of differentiated therapies that prioritize
women'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.
Daré’s first FDA-approved product, XACIATO™
(clindamycin phosphate) vaginal gel, 2% is 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. Daré’s portfolio also includes
potential first-in-category candidates in clinical development:
Ovaprene®, a novel, hormone-free monthly intravaginal contraceptive
whose U.S. commercial rights are under a license agreement with
Bayer; Sildenafil Cream, 3.6%, a novel cream formulation of
sildenafil to treat female sexual arousal disorder (FSAD) and/or
female sexual interest/arousal disorder (FSIAD) utilizing the
active ingredient in Viagra®; and DARE-HRT1, a combination
bio-identical estradiol and progesterone intravaginal ring for
menopausal hormone therapy. To learn more about XACIATO, Daré’s
full portfolio of women’s health product candidates, and Daré’s
mission to deliver differentiated therapies for women, please visit
www.darebioscience.com.
Daré may announce material information about its
finances, product and product candidates, clinical trials and other
matters using the Investors section of its website
(http://ir.darebioscience.com), SEC filings, press releases, public
conference calls and webcasts. Daré 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 Daré posts on its
investor relations website or through social media channels may be
deemed to be material information. Daré encourages investors, the
media, and others interested in the company to review the
information Daré posts in the Investors section of its website and
to follow these 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 Daré’s website.
Forward-Looking Statements
Daré 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
“believe,” “may,” “will,” “estimate,” “continue,” “anticipate,”
“design,” “intend,” “expect,” “could,” “plan,” “potential,”
“predict,” “seek,” “should,” “would,” “contemplate,” “project,”
“target,” “objective,” 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
commercial launch of XACIATO in the U.S., plans and expectations
with respect to Daré’s product candidates, including anticipated
timing for commencement and conduct of clinical trials,
announcement of topline results and meetings with the FDA, and the
anticipated FDA approval pathway for a product candidate, the
expectation that a product candidate could be a first-in-category
product, and the potential market size and opportunity for a
product candidate, if approved. Forward-looking statements involve
known and unknown risks, uncertainties and other factors that may
cause Daré’s 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: Daré’s ability to raise additional
capital when and as needed to advance its product candidates,
execute its business strategy and continue as a going concern; 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 development of a product candidate requires more
clinical or nonclinical studies than Daré anticipates; Daré’s
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; Daré’s
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; Daré’s dependence on third parties to conduct
clinical trials and manufacture and supply clinical trial material
and commercial product; the loss of, or inability to attract, key
personnel; the effects of macroeconomic conditions, geopolitical
events, and public health emergencies on Daré’s operations,
financial results and condition, and ability to achieve current
plans and objectives, including their potential impact on Daré’s
ability to timely commence, enroll, conduct and report results of
its clinical trials and on the ability of third parties on which
Daré relies to assist in the conduct of its business to fulfill
their contractual obligations to Daré; the impact of pharmaceutical
industry regulation and health care legislation in the United
States and internationally; the risk that developments by
competitors make Daré’s product or product candidates less
competitive or obsolete; difficulties establishing and sustaining
relationships with development and/or commercial collaborators;
failure of Daré’s product or product candidates, if approved, to
gain market acceptance or obtain adequate coverage or reimbursement
from third-party payers; Daré’s ability to retain its licensed
rights to develop and commercialize a product or product candidate;
Daré’s 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; Daré’s
ability to adequately protect or enforce its, or its licensor’s,
intellectual property rights; the lack of patent protection for the
active ingredients in certain of Daré’s 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 Daré’s product
or product candidates or the business activities of Daré, its
commercial collaborators or other third parties on which Daré
relies; the impact of pharmaceutical industry regulation and health
care legislation in the United States and internationally; global
trends toward health care cost containment; cyber attacks, security
breaches or similar events that compromise Daré’s technology
systems or those of third parties on which it relies and/or
significantly disrupt Daré’s business; and disputes or other
developments concerning Daré’s intellectual property rights. Daré’s
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 Daré’s risks and uncertainties, you are
encouraged to review its documents filed with the SEC including
Daré’s 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. Daré 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.
Contacts:
Investors on behalf of Daré Bioscience, Inc.:Lee Roth / Julia
WeilmanBurns McClellanlroth@burnsmc.com /
jweilman@burnsmc.com646.930.4406 / 646.732.4443
OR
Media on behalf of Daré Bioscience, Inc.:Jake RobisonEvoke
Canale jake.robison@evokegroup.com 619.849.5383
Source: Daré Bioscience, Inc.
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