Zentalis Pharmaceuticals Announces Key Management Appointments
12 Dezember 2024 - 1:00PM
Zentalis® Pharmaceuticals, Inc. (Nasdaq: ZNTL), a clinical-stage
biopharmaceutical company discovering and developing clinically
differentiated small molecule therapeutics targeting fundamental
biological pathways of cancers, today announced the appointment of
Wendy Chang as Chief People Officer and Haibo Wang as Chief
Business Officer.
"Zentalis is sharply focused on our goal of bringing azenosertib
to patients with gynecological malignancies,” said Julie Eastland,
Chief Executive Officer. “To support this goal, we are continuing
to tune our leadership team and today announced the appointment of
two talented leaders with a strong track record of successfully
supporting organizations through transitional periods. I look
forward to working with Wendy, Haibo, and the rest of the
leadership team as we advance the development of azenosertib.”
Executive BiographiesWendy Chang, Chief People
OfficerWendy is the Chief People Officer of Zentalis. She brings
over two decades of biopharma experience, including senior roles in
human resources and an extensive background in aligning talent with
organizations’ overall vision and direction. She was previously
Chief People Officer at Harpoon Therapeutics. Before Harpoon, she
was VP, Head of People & Culture for IDbyDNA. Wendy previously
served in roles of increasing responsibility at Gilead Sciences
from 2003 to 2020, most recently as Vice President, Human
Resources, and, earlier in her career, at Bio-Rad Laboratories. She
received a B.S. in accounting and business/management from the
University of California, Riverside, and completed the Global
Fellow of Talent Management program at The Wharton School of the
University of Pennsylvania.
Haibo Wang, Chief Business OfficerHaibo is the Chief Business
Officer of Zentalis. He brings over 15 years of biopharma business
development, finance, and M&A transaction experience, having
most recently served as Senior Vice President of Business
Development at Harpoon Therapeutics. While at Harpoon, he played a
pivotal role in managing the Company’s acquisition by Merck, which
was completed in March 2024. Prior to Harpoon, he served as the
Vice President of Business Development at Hummingbird Bioscience,
where he was responsible for the company’s end-to-end business
development activities. Prior to Hummingbird, Haibo was Director of
Business Development at Amgen, where he played a major role in the
Teneobio and Five Prime Therapeutics acquisitions, the oncology
collaboration with BeiGene, and many clinical collaborations to
advance Amgen’s oncology pipeline. He began his career as an
M&A consultant at Deloitte, advising on transactions in
healthcare and technology. Haibo holds an M.S. in Biotechnology
from Johns Hopkins University, an MBA from Duke University, and a
BBA from Tsinghua University.
About Zentalis Pharmaceuticals Zentalis®
Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company
discovering and developing clinically differentiated small molecule
therapeutics targeting fundamental biological pathways of cancers.
The Company’s lead product candidate, azenosertib (ZN-c3), is a
potentially first-in-class and best-in-class WEE1 inhibitor for
advanced solid tumors. Azenosertib is being evaluated as a
monotherapy and in combination across multiple clinical trials and
has broad franchise potential. In clinical trials, azenosertib has
been well tolerated and has demonstrated anti-tumor activity as a
single agent across multiple tumor types and in combination with
several chemotherapy backbones. As part of its azenosertib clinical
development program, the Company is exploring enrichment strategies
targeting tumors of high genomic instability, such as Cyclin E1
positive tumors, homologous recombination deficient tumors and
tumors with oncogenic driver mutations. The Company is also
leveraging its extensive experience and capabilities across cancer
biology and medicinal chemistry to advance its research on protein
degraders. Zentalis has operations in San Diego.
For more information, please visit www.zentalis.com. Follow
Zentalis on X/Twitter at @ZentalisP and on LinkedIn at
www.linkedin.com/company/zentalis-pharmaceuticals.
Forward-Looking StatementsThis
press release contains forward-looking statements within the
meaning of the U.S. Private Securities Litigation Reform Act of
1995. All statements contained in this press release that do not
relate to matters of historical fact should be considered
forward-looking statements, including statements regarding our goal
of bringing azenosertib to patients with gynecological
malignancies; the potential of azenosertib; the potential for
azenosertib to be first-in-class and best-in-class; the broad
franchise potential of azenosertib; and our plans with respect to
the development of product candidates, including azenosertib. The
terms “advance,” “goal,” “look forward,” "plan," “potential,”
“support,” “to be,” and “will” and similar references are intended
to identify forward-looking statements, although not all
forward-looking statements contain these identifying words. These
statements are neither promises nor guarantees, but involve known
and unknown risks, uncertainties and other important factors that
may cause our actual results, performance or achievements to be
materially different from any future results, performance or
achievements expressed or implied by the forward-looking
statements, including, but not limited to, the following: our
limited operating history, which may make it difficult to evaluate
our current business and predict our future success and viability;
we have and expect to continue to incur significant losses; our
need for additional funding, which may not be available; our plans,
including the costs thereof, of development of any diagnostic
tools; our substantial dependence on the success of our lead
product candidate, azenosertib; the outcome of preclinical testing
and early trials may not be predictive of the success of later
clinical trials; failure to identify additional product candidates
and develop or commercialize marketable products; potential
unforeseen events during clinical trials could cause delays or
other adverse consequences; risks relating to the regulatory
approval process or ongoing regulatory obligations; failure to
obtain U.S. or international marketing approval; our product
candidates may cause serious adverse side effects; inability to
maintain our collaborations, or the failure of these
collaborations; our reliance on third parties; effects of
significant competition; the possibility of system failures or
security breaches; risks relating to intellectual property; our
ability to attract, retain and motivate qualified personnel, and
risks relating to management transitions; significant costs as a
result of operating as a public company; and the other important
factors discussed under the caption “Risk Factors” in our most
recently filed periodic report on Form 10-K or 10-Q and subsequent
filings with the U.S. Securities and Exchange Commission (SEC) and
our other filings with the SEC. Any such forward-looking statements
represent management’s estimates as of the date of this press
release. While we may elect to update such forward-looking
statements at some point in the future, we disclaim any obligation
to do so, even if subsequent events cause our views to change.
ZENTALIS® and its associated logo are trademarks of Zentalis
and/or its affiliates. All website addresses and other links in
this press release are for information only and are not intended to
be an active link or to incorporate any website or other
information into this press release.
Contact:Elizabeth Pingpank
Hickinehickin@zentalis.com 860-463-0469
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