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NewAmsterdam to Present Full Data from ROSE2 at NLA Scientific Sessions 2023 NewAmsterdam to review data on webcast conference call on

Key Takeaway: NewAmsterdam Pharma Company N.V. is set to present full data from its ROSE2 trial at the National Lipid Association Scientific Sessions 2023. The late-breaking presentation will detail the efficacy of obicetrapib in combination with ezetimibe as an adjunct to high-intensity statin therapy. The company anticipates advancing to a definitive bioequivalence trial and a Phase 3 safety trial later this year. They aim to improve treatment options for cardiometabolic diseases, highlighting their innovative approach to LDL-C reduction in patients at high risk for cardiovascular diseases.

Market Sentiment Analysis

POSITIVE FACTORS

  • NewAmsterdam will present full data from their ROSE2 trial at a major conference, showcasing their research progress.
  • The combination therapy of obicetrapib and ezetimibe demonstrated a significant median reduction in LDL-C levels, suggesting effectiveness.
  • The company has substantial financial backing with $328 million obtained from their recent business combination.

Full Press Release Details

NewAmsterdam to Present Full Data from ROSE2 at NLA Scientific Sessions 2023
NewAmsterdam to review data on webcast conference call on June 5, 2023 at 8:00 a.m. ET
Naarden, the Netherlands and Miami, USA; May 23, 2023 NewAmsterdam Pharma Company N.V. (Nasdaq: NAMS or
NewAmsterdam or the Company ), a clinical-stage company focused on the research and development of transformative oral therapies for major cardiometabolic diseases, today announced that it will present full data from ROSE2, a
Phase 2 clinical trial evaluating obicetrapib in combination with ezetimibe as an adjunct to high-intensity statin therapy, in a late-breaking presentation at the National Lipid Association ( NLA ) Scientific Sessions, being held June 1-4 in Atlanta, Georgia. NewAmsterdam is developing a fixed dose combination of obicetrapib 10 mg and ezetimibe 10 mg, and expects to select a formulation to advance into a definitive bioequivalence trial and a
Phase 3 safety and efficacy trial in the second half of 2023.
Details of the presentation are as follows:
Presentation Title: The combination of Obicetrapib and Ezetimibe lowers LDL-C in Patients on High Intensity
Statins: Results from the ROSE2 Trial (NCT05266586)
Session Title: Late-Breaker Session
Session Date and Time: Saturday, June 3, 2023, 12:00 P.M. ET
Location: Omni Atlanta Hotel at CNN Center
and Analyst Conference Call and Live Webcast
NewAmsterdam will host a conference call for investors and analysts to review the full data from ROSE2.
The live webcast will begin at 8:00 a.m. ET on Monday, June 5 and will include remarks by Robert Rosenson, M.D., a Professor of Medicine and Director of Cardiometabolic Disorders at the Icahn School of Medicine at Mount Sinai.
Participants may register for the conference call here. While not required, it is recommended that participants join the call ten minutes prior to the
A live webcast of the call will also be available under Events & Presentations in the Investors & News
section of the Company s website at https://ir.newamsterdampharma.com. The archived webcast will be available on NewAmsterdam s website approximately two hours after the conference call and will be available for at least 30 days following
(Nasdaq: NAMS) is a clinical-stage biopharmaceutical company whose mission is to improve patient care in populations with cardiometabolic diseases where currently approved therapies have not been sufficiently successful or well tolerated.
NewAmsterdam is investigating obicetrapib, an oral, low-dose and once-daily CETP inhibitor, as the preferred LDL-C lowering therapy to be used as an adjunct to
maximally-tolerated statin therapy for high-risk cardiovascular disease ( CVD ) patients. Results from NewAmsterdam s ROSE Phase 2b trial (presented at AHA Scientific Sessions in 2021) included observations that patients receiving
obicetrapib 10 mg experienced a median reduction in LDL-C of 51% versus baseline in patients on high-intensity statin therapy (vs. a 7% reduction in the placebo arm). In addition, topline results from
NewAmsterdam s ROSE2 trial evaluating the combination of 10 mg obicetrapib and 10 mg ezetimibe demonstrated a median reduction in LDL-C levels of 59% versus baseline in patients on high-intensity statin
therapy (vs. a 6% reduction in the placebo arm). Based in the Netherlands, NewAmsterdam recently completed a business combination with FLAC, a special purpose acquisition company sponsored by an affiliate of Frazier Healthcare Partners. Proceeds
from this transaction were approximately $328 million, prior to deducting transaction expenses. In June 2022, NewAmsterdam entered into an exclusive licensing agreement with the Menarini Group for the commercialization of obicetrapib in Europe,
while retaining all rights to commercialize obicetrapib, if approved, in the rest of the world, as well as rights to develop certain forms of obicetrapib for other diseases such as Alzheimer s disease. For more information, please visit:
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 clinical trials and the timing for enrolling patients, the timing and forums for announcing data and the achievement and timing of regulatory approvals. 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
relating to the uncertainty of the projected financial information with respect to the Company; risks related to the approval of the Company s product candidate and the timing of expected regulatory and business milestones; ability to negotiate
definitive contractual arrangements with potential customers; the impact of competitive product candidates; ability to obtain sufficient supply of materials; the impact of COVID-19; global economic and
political conditions, including the Russia-Ukraine conflict; the effects of competition on the Company s future business; and those factors described in the Company s public filings with the U.S. Securities and 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.
Spectrum Science on behalf of NewAmsterdam
Stern Investor Relations on behalf of NewAmsterdam

Frequently Asked Questions

What is the ROSE2 trial about?

The ROSE2 trial evaluates obicetrapib combined with ezetimibe alongside high-intensity statin therapy.

When will NewAmsterdam present ROSE2 data?

NewAmsterdam will present full ROSE2 data on June 3, 2023, at 12:00 P.M. ET.

How can I access the live webcast of the call?

The live webcast starts on June 5, 2023, at 8:00 a.m. ET and will be available online.

What is the expected LDL-C reduction from obicetrapib?

Obicetrapib is associated with a median LDL-C reduction of 59% in high-intensity statin patients.

Where is NewAmsterdam Pharma based?

NewAmsterdam Pharma Company is based in Naarden, the Netherlands.

Last updated: May 23, 2023