NewAmsterdam Pharma Company N.V. (Nasdaq: NAMS or “NewAmsterdam” or
the “Company”), a late-stage, clinical biopharmaceutical company
developing oral, non-statin medicines for patients at risk of
cardiovascular disease (“CVD”) with elevated low-density
lipoprotein cholesterol (“LDL-C”), for whom existing therapies are
not sufficiently effective or well-tolerated, today announced the
appointments of Mark C. McKenna and Wouter Joustra to its Board of
Directors. Mr. McKenna and Mr. Joustra have joined as temporary
non-executive directors to fulfill vacant positions within the
Board of Directors until their proposed appointment by the general
meeting of shareholders at the next annual general meeting.
Additionally, NewAmsterdam announced the departure of Sander
Slootweg from its Board of Directors, effective July 16, 2024.
“On behalf of the NewAmsterdam team, we are
delighted to welcome Wouter and Mark to our Board of Directors.
Wouter’s strategic leadership of Forbion’s public market investment
strategy and his history with NewAmsterdam will be valuable as we
approach our expected pivotal Phase 3 data readouts from multiple
ongoing clinical trials. Additionally, we look forward to
leveraging Mark’s extraordinary career and deep experience in
building world class organizations as we approach these expected
milestones,” said Michael Davidson, M.D., Chief Executive Officer
of NewAmsterdam. “The Board and I would like to express our
collective gratitude to Sander for his contributions and dedication
to the success of the organization. We wish him the best as he
focuses his attention on venture investments at Forbion.”
Mr. McKenna brings over 20 years of
pharmaceutical industry experience and executive leadership to
NewAmsterdam’s Board. He is the founder, Chairman and Chief
Executive Officer of Mirador Therapeutics, Inc., and currently
serves as Chairman of the board of directors of Apogee
Therapeutics, Inc. (Nasdaq: APGE) and a director at Spyre
Therapeutics, Inc. (Nasdaq: SYRE). In addition, Mr. McKenna serves
as a venture partner at Arch Venture Partners and Senior Advisor at
Fairmount Funds. Previously, Mr. McKenna was President, Chief
Executive Officer and Chairman of the Board of Directors of
Prometheus Biosciences, Inc., which was acquired by Merck &
Co., Inc. in June 2023 for approximately $10.8 billion. Earlier,
Mr. McKenna was a corporate officer of Bausch Health and served as
President of its subsidiary, Salix Pharmaceuticals, Inc. Prior to
Salix Pharmaceuticals, Mr. McKenna spent more than a decade in
various roles with Bausch + Lomb, also a division of Bausch Health,
most recently as Senior Vice President and General Manager of its
U.S. Vision Care business. Mr. McKenna was Ernst & Young’s
Entrepreneur of the Year in 2023 and holds a B.S. in marketing from
Arizona State University and an M.B.A. from Azusa Pacific
University.
"Throughout my career, I have been fortunate to
serve companies leading in innovation, witnessing firsthand the
profound impact on patients and families,” said Mr. McKenna. “With
multiple Phase 3 trial readouts on the horizon and an exemplary
management team at the helm, I believe NewAmsterdam is
well-positioned to make a significant impact on the CVD landscape.
I am excited to collaborate with management and the Board to help
the Company achieve its mission."
Mr. Joustra brings multiple years of industry
executive leadership, as well as deep capital markets and life
sciences investment experience to NewAmsterdam. Mr. Joustra is a
General Partner at Forbion, a leading global life sciences venture
capital firm with deep expertise in Europe. At Forbion, Mr.
Woustra’s responsibilities include deal origination, general
portfolio management and divestment strategies, with a focus on
Forbion’s Growth Opportunities Funds, which invests in late-stage
life sciences companies. Prior to joining Forbion in 2019, Mr.
Joustra was a Senior Trader and Executive Board member of the life
sciences franchise at Kempen, a European boutique investment bank.
In this role he managed the bank’s trading portfolio and was
involved in deal structuring and equity capital markets
transactions, and larger block trades.
Mr. Joustra previously served as a member of the
board of directors of several companies, including: Gyroscope
Therapeutics Holdings plc until its acquisition by Novartis AG in
February 2022, VectivBio AG (Nasdaq: VECT) from December 2022 until
its acquisition by Ironwood Pharmaceuticals, Inc. in December 2023,
Aiolos Bio, Inc. until its acquisition by GSK plc in February 2024
and Forbion European Acquisition Corporation, a special purpose
acquisition company, until its completion of the business
combination with enGene Holdings Inc. in October 2023.
Currently Mr. Joustra serves on the board of
directors of VectorY Therapeutics, Beacon Therapeutics and enGene
Holdings Inc. (Nasdaq: ENGN). He holds an M.Sc. in Business
Administration from the University of Groningen, and a B.Sc. in
International Business and Management from this same
university.
“I am excited to join the Board during this
exciting time in NewAmsterdam’s history and to continue Forbion’s
contribution to the Company,” said Mr. Joustra. “Based on clinical
data to date, I believe obicetrapib has the potential to play a
critical role in the lipid-lowering and CVD treatment landscapes
for millions of patients globally, if approved. I have had the
opportunity to work closely with the NewAmsterdam Board and the
entire team for over three years and, together with the Forbion
team, I am eager to continue supporting the Company’s important
efforts to improve patient care.”
About NewAmsterdam
NewAmsterdam Pharma (Nasdaq: NAMS) is a
late-stage biopharmaceutical company whose mission is to improve
patient care in populations with metabolic diseases where currently
approved therapies have not been adequate or well tolerated. We
seek to fill a significant unmet need for a safe, well-tolerated
and convenient LDL-lowering therapy. In multiple phase 3 studies,
NewAmsterdam is investigating obicetrapib, an oral, low-dose and
once-daily CETP inhibitor, alone or as a fixed-dose combination
with ezetimibe, as LDL-C lowering therapies to be used as an
adjunct to statin therapy for patients at risk of CVD with elevated
LDL-C, for whom existing therapies are not sufficiently effective
or well tolerated.
Forward-Looking Statements
Certain statements included in this document
that are not historical facts are forward-looking statements for
purposes of the safe harbor provisions under the United States
Private Securities Litigation Reform Act of 1995. Forward-looking
statements generally are accompanied by words such as “believe,”
“may,” “will,” “estimate,” “continue,” “anticipate,” “intend,”
“expect,” “should,” “would,” “plan,” “predict,” “potential,”
“seem,” “seek,” “future,” “outlook” and similar expressions that
predict or indicate future events or trends or that are not
statements of historical matters. These forward-looking statements
include, but are not limited to, statements regarding the Company’s
business and strategic plans, the Company’s commercial opportunity,
the therapeutic and curative potential of the Company’s product
candidate, the Company’s clinical trials and the timing for
enrolling patients, the timing and forums for announcing data, the
achievement and timing of regulatory approvals, and plans for
commercialization. These statements are based on various
assumptions, whether or not identified in this document, and on the
current expectations of the Company’s management and are not
predictions of actual performance. These forward-looking statements
are provided for illustrative purposes only and are not intended to
serve as and must not be relied on as a guarantee, an assurance, a
prediction, or a definitive statement of fact or probability.
Actual events and circumstances are difficult or impossible to
predict and may differ from assumptions. Many actual events and
circumstances are beyond the control of the Company. These
forward-looking statements are subject to a number of risks and
uncertainties, including changes in domestic and foreign business,
market, financial, political, and legal conditions; risks related
to the approval of the Company’s product candidate and the timing
of expected regulatory and business milestones, including potential
commercialization; ability to negotiate definitive contractual
arrangements with potential customers; the impact of competitive
product candidates; ability to obtain sufficient supply of
materials; global economic and political conditions, including the
Russia-Ukraine and Israel-Hamas conflicts; the effects of
competition on the Company’s future business; and those factors
described in the Company’s public filings with the Securities
Exchange Commission. Additional risks related to the Company’s
business include, but are not limited to: uncertainty regarding
outcomes of the Company’s ongoing clinical trials, particularly as
they relate to regulatory review and potential approval for its
product candidate; risks associated with the Company’s efforts to
commercialize a product candidate; the Company’s ability to
negotiate and enter into definitive agreements on favorable terms,
if at all; the impact of competing product candidates on the
Company’s business; intellectual property related claims; the
Company’s ability to attract and retain qualified personnel;
ability to continue to source the raw materials for its product
candidate. If any of these risks materialize or the Company’s
assumptions prove incorrect, actual results could differ materially
from the results implied by these forward-looking statements. There
may be additional risks that the Company does not presently know or
that the Company 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 the Company’s expectations, plans, or forecasts of future
events and views as of the date of this document and are qualified
in their entirety by reference to the cautionary statements herein.
The Company anticipates that subsequent events and developments may
cause the Company’s assessments to change. These forward-looking
statements should not be relied upon as representing the Company’s
assessment as of any date subsequent to the date of this
communication. Accordingly, undue reliance should not be placed
upon the forward-looking statements. Neither the Company nor any of
its affiliates undertakes any obligation to update these
forward-looking statements, except as may be required by law.
Company ContactMatthew
PhilippeP:
1-917-882-7512matthew.philippe@newamsterdampharma.com
Media ContactSpectrum Science
on behalf of NewAmsterdamBryan BlatsteinP:
1-917-714-2609bblatstein@spectrumscience.com
Investor ContactPrecision AQ on
behalf of NewAmsterdamAustin MurtaghP:
1-212-698-8696austin.murtagh@precisionaq.com
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