Aspira Women’s Health Announces Appointment of Dr. Sandra Milligan as Interim CEO
17 December 2024 - 12:45AM
Aspira Women’s Health Inc. (“Aspira” or the “Company”) (NASDAQ:
AWH), a bio-analytical based women’s health company focused on the
development of gynecologic disease diagnostic tools, today
announced that Nicole Sandford, Chief Executive Officer (CEO) and
Board member, will be departing the Company to focus on a family
health matter. Aspira’s President Dr. Sandra Milligan will step
into the role of interim CEO while a nationwide search of internal
and external candidates is conducted. Ms. Sandford’s departure will
be effective immediately. She will remain as a consultant to ensure
a seamless transition.
“The Board thanks Nicole for the outstanding work she has done
in stabilizing the business, building a first-class team, and
putting the company on solid footing for the next phase of growth,”
said Ms. Jannie Herchuk, Chairwoman of the Board at Aspira. “During
her tenure as CEO, Aspira launched its OvaWatch multivariate assay,
a significant expansion of our commercial ovarian cancer portfolio,
and received a $10 million award from the Advanced Research
Projects Agency for Health to complete the company’s endometriosis
detection product. Her contributions helped bring us to a critical
inflection point for Aspira.”
“Sandy Milligan has a deep understanding of Aspira’s technology
and vision and is well-positioned to oversee the continued
execution of the Company’s long-term growth strategy as we search
for a permanent successor,” Ms. Herchuk continued.
About Aspira Women’s Health Inc. Aspira
Women’s Health Inc. is dedicated to the discovery, development, and
commercialization of noninvasive, AI-powered tests to aid in the
diagnosis of gynecologic diseases.
OvaWatch® and Ova1Plus® are offered to clinicians as OvaSuiteSM.
Together, they provide the only comprehensive portfolio of blood
tests to aid in the detection of ovarian cancer risk for the 1.2+
million American women diagnosed with an adnexal mass each year.
OvaWatch provides a negative predictive value of 99% and is used to
assess ovarian cancer risk for women where initial clinical
assessment indicates the mass is indeterminate or benign, and thus
surgery may be premature or unnecessary. Ova1Plus is a reflex
process of two FDA-cleared tests, Ova1® and Overa®, to assess the
risk of ovarian malignancy in women with an adnexal mass planned
for surgery.
Our in-development test pipeline will expand our ovarian cancer
portfolio and address the tremendous need for non-invasive
diagnostics for endometriosis, a debilitating disease that impacts
millions of women worldwide. In ovarian cancer, we intend to
combine microRNA and protein biomarkers with patient data to
further enhance the sensitivity and specificity of our current
tests. In endometriosis, we have developed the first-ever
non-invasive test designed to identify endometriomas, one of the
most commonly occurring forms of severe endometriosis. Through our
ongoing endometriosis development program, we are combining
microRNA and protein biomarkers with patient data, with the intent
of identifying all endometriosis independent of disease location or
severity.
Forward-Looking Statements This press release
contains forward-looking statements, as defined in the Private
Securities Litigation Reform Act of 1995. Forward-looking
statements involve a number of risks and uncertainties. Such
forward-looking statements include statements regarding, among
other things, the timing and completion of any products in the
development pipeline and other statements that are predictive in
nature, and whether the marketing of the OvaSuite portfolio will
prove successful. Actual results could differ materially from those
discussed due to known and unknown risks, uncertainties, and other
factors. These forward-looking statements generally can be
identified by the use of words such as “designed to,” “expect,”
“plan,” “anticipate,” “could,” “may,” “intend,” “will,” “continue,”
“future,” and other words of similar meaning and the use of future
dates. These and additional risks and uncertainties are described
more fully in the Company’s filings with the SEC, including those
factors identified as “Risk Factors” in our most recent Annual
Report on Form 10-K, for the fiscal year ended December 31, 2023,
and subsequent Quarterly Reports on Form 10-Q. If any of these
risks materialize or our assumptions prove incorrect, actual
results could differ materially from the results implied by these
forward-looking statements. There may be additional risks that
Aspira presently does not know, or that Aspira currently believes
are immaterial, that could also cause actual results to differ from
those contained in the forward-looking statements. In addition,
forward-looking statements reflect Aspira’s expectations, plans, or
forecasts of future events and views as of the date of this press
release. Subsequent events and developments may cause the Company’s
assessments to change. However, while Aspira may elect to update
these forward-looking statements at some point in the future,
Aspira expressly disclaims any obligation to do so, except as
required by law. These forward-looking statements should not be
relied upon as representing Aspira’s assessments of any date after
the date of this press release. Accordingly, undue reliance should
not be placed upon the forward-looking statements.
Investor Relations Contact: Mike CavanaughICR
Healthcaremike.cavanaugh@icrhealthcare.com
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