Kadmon Announces Appointment of David E. Cohen, M.D., MPH, to Board of Directors
07 Febrero 2019 - 3:15PM
Kadmon Holdings, Inc. (NYSE: KDMN) today announced the appointment
of David E. Cohen, M.D., MPH, to its Board of Directors. Dr. Cohen
has held a variety of positions at the New York University School
of Medicine, including as Chief of Allergy and Contact Dermatitis,
Vice Chairman of Clinical Affairs, Director of Occupational and
Environmental Dermatology, and the Charles C. and Dorothea E.
Harris Professor of Dermatology.
“David brings to Kadmon a deep understanding of
the research and treatment of immune and fibrotic disorders, which
aligns perfectly with our near-term focus to bring promising new
products to market in these therapeutic areas,” said Harlan W.
Waksal, M.D., President and CEO at Kadmon. “David’s clinical
expertise, along with his board and consultancy experience at
several healthcare companies, will enrich the scientific acumen of
our board and better position Kadmon for continued clinical
progress.”
Dr. Cohen is the Charles C. and Dorothea E.
Harris Professor of Dermatology at New York University School of
Medicine, where he also serves as Chief of Allergy and Contact
Dermatitis, Vice Chairman of Clinical Affairs, and Director of
Occupational and Environmental Dermatology. Dr. Cohen joined the
NYU faculty in 1994 and his work has concentrated on cutaneous
allergic and toxic reactions to exogenous and photo-reactive
chemicals and the interaction of environmental stressors on the
skin. Dr. Cohen has previously served as a lecturer of
Environmental Sciences at Columbia University School of Public
Health. Dr. Cohen has been a member of the board of directors of
Dermira since 2014 and had previously served as a scientific
advisor to Dermira since its inception in 2010. Dr. Cohen served on
the boards of directors of Vyteris from 2011 to 2012 and Connetics
from 2005 until its sale to Stiefel in 2006.
Dr. Cohen is the Past President of the American
Dermatological Association, and served as President of the American
Contact Dermatitis Society, the Dermatology Section of the New York
Academy of Medicine, and the New York Dermatological Association.
He served as a founding board member for the American Acne and
Rosacea Society, and led the national guidelines of care for
individuals with Latex allergy and served on the panel to establish
the national guidelines of care for Atopic Dermatitis for the
American Academy of Dermatology. Dr. Cohen received his M.D. from
the State University of New York at Stony Brook School of Medicine,
his MPH at Columbia University, and served as an Intern at Columbia
Presbyterian Medical Center, a Dermatology resident from the New
York University Medical Center and a resident in Occupational and
Environmental Medicine from Columbia University School of Public
Health. Dr. Cohen received his B.S. from the City University of New
York.
About Kadmon Holdings,
Inc.
Kadmon Holdings, Inc. is a fully integrated
biopharmaceutical company developing innovative product candidates
for significant unmet medical needs. Our product pipeline is
focused on inflammatory and fibrotic diseases.
Forward Looking Statements
This press release contains forward-looking
statements. Such statements may be preceded by the words “may,”
“will,” “should,” “expects,” “plans,” “anticipates,” “could,”
“intends,” “targets,” “projects,” “contemplates,” “believes,”
“estimates,” “predicts,” “potential” or “continue” or the negative
of these terms or other similar expressions. Forward-looking
statements 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. We believe that these factors include,
but are not limited to, (i) the initiation, timing, progress and
results of our preclinical studies and clinical trials, and our
research and development programs; (ii) our ability to advance
product candidates into, and successfully complete, clinical
trials; (iii) our reliance on the success of our product
candidates; (iv) the timing or likelihood of regulatory filings and
approvals; (v) our ability to expand our sales and marketing
capabilities; (vi) the commercialization of our product candidates,
if approved; (vii) the pricing and reimbursement of our product
candidates, if approved; (viii) the implementation of our business
model, strategic plans for our business, product candidates and
technology; (ix) the scope of protection we are able to establish
and maintain for intellectual property rights covering our product
candidates and technology; (x) our ability to operate our business
without infringing the intellectual property rights and proprietary
technology of third parties; (xi) costs associated with defending
intellectual property infringement, product liability and other
claims; (xii) regulatory developments in the United States, Europe
and other jurisdictions; (xiii) estimates of our expenses, future
revenues, capital requirements and our needs for additional
financing; (xiv) the potential benefits of strategic collaboration
agreements and our ability to enter into strategic arrangements;
(xv) our ability to maintain and establish collaborations or obtain
additional grant funding; (xvi) the rate and degree of market
acceptance of our product candidates; (xvii) developments relating
to our competitors and our industry, including competing therapies;
(xviii) our ability to effectively manage our anticipated growth;
(xix) our ability to attract and retain qualified employees and key
personnel; (xx) our ability to achieve cost savings and other
benefits from our efforts to streamline our operations and to not
harm our business with such efforts; (xxi) the use of proceeds from
our recent public offerings; (xxii) the potential benefits of any
of our product candidates being granted orphan drug
designation; (xxiii) the future trading price of the shares
of our common stock and impact of securities analysts’ reports on
these prices; and/or (xxiv) other risks and uncertainties. More
detailed information about Kadmon and the risk factors that may
affect the realization of forward-looking statements is set forth
in the Company’s filings with the U.S. Securities and Exchange
Commission (the “SEC”), including the Company’s Annual Report on
Form 10-K for the fiscal year ended December 31, 2017 and the
Company’s Quarterly Report on Form 10-Q filed pursuant to Section
13 of the Securities Exchange Act of 1934, as amended, with the SEC
on November 9, 2018. Investors and security holders are urged to
read these documents free of charge on the SEC’s website at
www.sec.gov. The Company assumes no obligation to publicly update
or revise its forward-looking statements as a result of new
information, future events or otherwise.
Contact InformationEllen
Cavaleri, Investor
Relations646.490.2989ellen.cavaleri@kadmon.com
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