Disc Medicine Expands Leadership Team with Appointment of Industry Veteran Steve Caffé, MD as Chief Regulatory Officer
19 Settembre 2024 - 2:30PM
Disc Medicine, Inc. (NASDAQ:IRON), a clinical-stage
biopharmaceutical company focused on the discovery, development,
and commercialization of novel treatments for patients suffering
from serious hematologic diseases, today announced the appointment
of Steve Caffé, MD as the company’s Chief Regulatory Officer. Dr.
Caffé is an experienced biotech executive with significant
expertise in global regulatory leadership across a wide range of
therapeutic areas, including hematology, oncology, and rare
diseases.
“We are excited to welcome an executive as accomplished as Steve
to Disc, where his depth of regulatory expertise and experience in
global product development will be integral to the company’s
growth,” said John Quisel, J.D., Ph.D., President and Chief
Executive Officer of Disc. “Steve’s track record of successful drug
approvals across multiple disease areas and geographies will be a
significant advantage for Disc as we move into the later stages of
development across our portfolio.”
“I am excited to be joining Disc at this pivotal moment in the
company’s transition to a late-stage hematology company,” said Dr.
Caffé. “With significant trial initiations coming in the next year
for all three pipeline programs, I look forward to leading global
regulatory interactions to support Disc’s mission of delivering
novel treatments to patients with high unmet need. I am excited to
work with the talented team at Disc and build on the excellent work
done to date.”
Dr. Caffé has more than 25 years of experience in global product
development and regulatory affairs, having held senior leadership
positions at several top biotechnology companies. Most recently, he
served as Head of Regulatory Affairs at CRISPR Therapeutics where
he was involved in the development and approval of Casgevy®
(exagamglogene autotemcel) for sickle cell disease and beta
thalassemia. Prior to joining CRISPR, Dr Caffé was the Senior Vice
President leading Regulatory Affairs, Pharmacovigilance, Quality,
and Patient Advocacy at Ra Pharmaceuticals. Before this, Dr. Caffé
held senior-level regulatory positions at a number of other
biopharmaceutical companies, including Sucampo Pharmaceuticals,
AMAG Pharmaceuticals, MedImmune (Biologics Division of
AstraZeneca), Baxter, Sanofi-Aventis and Merck. Across these
experiences, Dr. Caffé has contributed to over 40 new drug
approvals and major new indications worldwide in a wide range of
therapeutic areas. Steve received his M.D. at the Université Pierre
et Marie Curie in Paris, France.
In connection with Dr. Caffé’s appointment, on September 16,
2024, Disc granted to Dr. Caffé an inducement equity award outside
of Disc’s Amended and Restated 2021 Stock Option and Incentive Plan
in accordance with Nasdaq Listing Rule 5635(c)(4), comprised of (i)
an option to purchase 55,000 shares (the “Option Award”) of Disc’s
common stock (“Common Stock”), at an exercise price equal to the
closing price of the Common Stock on the date of grant, and (ii) a
restricted stock unit award for 36,666 shares of Common Stock (the
“RSU Award” and, together with the Option Award, the “Inducement
Award”). The Option Award shall vest 25% on September 16, 2025,
with the remainder vesting in 36 equal monthly installments
thereafter. The RSU Award shall vest in equal installments on each
of the first, second, third, and fourth anniversaries of the
vesting date set by Disc’s company vesting policy. The Inducement
Award was approved by the Compensation Committee of Disc’s Board of
Directors.
About Disc Medicine
Disc Medicine (NASDAQ:IRON) is a clinical-stage
biopharmaceutical company committed to discovering, developing, and
commercializing novel treatments for patients who suffer from
serious hematologic diseases. We are building a portfolio of
innovative, potentially first-in-class therapeutic candidates that
aim to address a wide spectrum of hematologic diseases by targeting
fundamental biological pathways of red blood cell biology,
specifically heme biosynthesis and iron homeostasis. For more
information, please visit www.discmedicine.com.
Disc Cautionary Statement Regarding Forward-Looking
Statements
This press release contains “forward-looking statements” within
the meaning of the Private Securities Litigation Reform Act of
1995, including, but not limited to, express or implied statements
regarding Disc’s expectations with respect to the chief regulatory
officer position, upcoming trial initiations in the next year, and
Disc’s clinical development plans and related regulatory
interactions. The use of words such as, but not limited to,
“believe,” “expect,” “estimate,” “project,” “intend,” “future,”
“potential,” “look forward,” “continue,” “may,” “might,” “plan,”
“will,” “should,” “seek,” “anticipate,” or “could” or the negative
of these terms and other similar words or expressions that are
intended to identify forward-looking statements. Forward-looking
statements are neither historical facts nor assurances of future
performance. Instead, they are based on Disc’s current beliefs,
expectations and assumptions regarding the future of Disc’s
business, future plans and strategies, clinical results and other
future conditions. New risks and uncertainties may emerge from time
to time, and it is not possible to predict all risks and
uncertainties. No representations or warranties (expressed or
implied) are made about the accuracy of any such forward-looking
statements.
Disc may not actually achieve the plans, intentions or
expectations disclosed in these forward-looking statements, and
investors should not place undue reliance on these forward-looking
statements. Actual results or events could differ materially from
the plans, intentions and expectations disclosed in the
forward-looking statements as a result of a number of material
risks and uncertainties including but not limited to: Disc’s
expectations regarding the chief regulatory officer position;
Disc’s expectations regarding leadership and future growth; Disc’s
expectations regarding its research and development programs;
Disc’s expectations of entering late-stage development; and the
other risks and uncertainties described in Disc’s filings with the
Securities and Exchange Commission, including in the “Risk Factors”
section of our Annual Report on Form 10-K for the year ended
December 31, 2023, and in subsequent Quarterly Reports on Form
10-Q. Any forward-looking statement speaks only as of the date on
which it was made. None of Disc, nor its affiliates, advisors or
representatives, undertake any obligation to publicly update or
revise any forward-looking statement, whether as result of new
information, future events or otherwise, except as required by
law.
Media Contact
Peg RusconiDeerfield Grouppeg.rusconi@deerfieldgroup.com
Investor Relations Contact
Christina TartagliaPrecision
AQchristina.tartaglia@precisionaq.com
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