NewAmsterdam Pharma to Host R&D Day with Key Opinion Leaders on May 16, 2024
02 May 2024 - 10:00PM
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 that
it will host an R&D Day event for analysts and investors on May
16, 2024 beginning at 9:00 a.m. ET in New York City.
Michael Davidson, M.D., Chief
Executive Officer, John Kastelein, M.D., Ph.D.,
FESC, Founder and Chief Scientific Officer, BJ
Jones, Chief Commercial Officer, Douglas
Kling, Chief Operating Officer and Ian
Somaiya, Chief Financial Officer, will be joined by
renowned cardiovascular disease specialists to discuss
obicetrapib’s clinical development path, NewAmsterdam’s commercial
readiness and strategy, and the cardiovascular disease landscape
and opportunities for innovative new products.
Renowned cardiovascular disease specialists will include:
- Jorge Plutzky,
M.D., Director of Preventative Cardiology at Brigham and
Women’s Hospital and Associate Professor at Harvard Medical
School;
- Ann Marie Navar, M.D.,
Ph.D., Associate Professor of Cardiology at UT
Southwestern Medical Center; and
- Ashish Sarraju,
M.D., Cardiologist at Cleveland Clinic’s Tomsich Family
Department of Cardiovascular Medicine Department and the Miller
Family Heart, Vascular & Thoracic Institute and researcher at
the Cleveland Clinic Coordinating Center for Clinical
Research.
A live webcast of the R&D event will be available and those
who intend to join virtually can pre-register for the webcast
through the link here. The live webcast and supporting presentation
materials will be available on the Events section of the Investor
Relations page of the NewAmsterdam website at
ir.newamsterdampharma.com at the time of the live event. An
archived replay will be available on the NewAmsterdam website.
Please note advanced registration is required for in-person
attendance.
About ObicetrapibObicetrapib is a novel, oral,
low-dose CETP inhibitor that NewAmsterdam is developing to overcome
the limitations of current LDL-lowering treatments. In each of the
Company’s Phase 2 trials, ROSE2, TULIP, ROSE, and OCEAN, evaluating
obicetrapib as monotherapy or combination therapy, the Company
observed statistically significant LDL-lowering combined with a
side effect profile similar to that of placebo. The Company is
conducting two Phase 3 pivotal trials, BROADWAY and BROOKLYN, to
evaluate obicetrapib as a monotherapy used as an adjunct to
maximally tolerated lipid-lowering therapies to provide additional
LDL-lowering for CVD patients and TANDEM, to evaluate obicetrapib
and ezetimibe as a fixed-dose combination. The Company began
enrolling patients in BROADWAY in January 2022, in BROOKLYN in July
2022, and in TANDEM in March 2024; completing enrollment of
BROOKLYN in April 2023 and BROADWAY in July 2023. The Company also
commenced the Phase 3 PREVAIL cardiovascular outcomes trial in
March 2022, which is designed to assess the potential of
obicetrapib to reduce occurrences of major adverse cardiovascular
events, including cardiovascular death, non-fatal myocardial
infarction, non-fatal stroke and non-elective coronary
revascularization. NewAmsterdam completed enrollment of PREVAIL in
April 2024 and randomized over 9,000 patients.
About NewAmsterdamNewAmsterdam 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.
Company ContactMatthew PhilippeP:
1-917-882-7512matthew.philippe@newamsterdampharma.com
Media ContactSpectrum Science on behalf of
NewAmsterdamJen GordonP:
1-202-957-7795jgordon@spectrumscience.com
Investor ContactStern Investor Relations on
behalf of NewAmsterdamHannah DeresiewiczP:
1-212-362-1200hannah.deresiewicz@sternir.com
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