This presentation contains "forward-looking" statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995, including, but not limited to: our plans to develop and commercialize small molecule therapies, our expectations about timing and ability to commence, enroll or complete clinical studies and to obtain regulatory approvals for PRT543, PRT811, PRT1419, PRT2527, PRT3645 and other candidates in development, the ability of our product candidates to treat various cancers, the ability to discover additional suitable candidates for regulatory approval, the potential impact of the COVID-19 pandemic and the sufficiency of our cash and cash equivalents to fund our operations.
Any statements contained herein or provided orally that are not statements of historical fact may be deemed to be forward-looking statements. In some cases, you can identify forward-looking statements by such terminology as ''believe,'' ''may,'' ''will,'' ''potentially,'' ''estimate,'' ''continue,'' ''anticipate,'' ''intend,'' ''could,'' ''would,'' ''project,'' ''plan,'' ''expect'' and similar expressions that convey uncertainty of future events or outcomes, although not all forward-looking statements contain these words. Statements, including forward-looking statements, speak only to the date they are provided (unless an earlier date is indicated).
These forward-looking statements are based on the beliefs of our management as well as assumptions made by and information currently available to us. Although we believe the expectations reflected in such forward-looking statements are reasonable, we can give no assurance that such expectations will prove to be correct. If such assumptions do not fully materialize or prove incorrect, the events or circumstances referred to in the forward-looking statements may not occur. We undertake no obligation to update publicly any forward-looking statements for any reason after the date of this presentation to conform these statements to actual results or to changes in our expectations, except as required by law. Accordingly, readers are cautioned not to place undue reliance on these forward-looking statements. Additional risks and uncertainties that could affect our business are included under the caption "Risk Factors" in our Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission for the three months ended June 30, 2022 and in our Annual Report on Form 10-K for the year ended December 31, 2021.
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Prelude Therapeutics: Vision
Build a fully integrated oncology company on the foundation of drug discovery excellence to deliver novel precision cancer medicines to underserved patients
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Prelude Therapeutics: Key Reasons to Invest
Internal
Effective
Strong
Discovery
R&D
Execution
Engine
Approach
Scientists with
Seamless
Proprietary
proven track
integration
diversified
records
between biology
pipeline
and chemistry
Focused
Clinical
Development
Driving to 'go/ no go' decisions
with a sense of
urgency
Well
Capitalized
~$246M cash
marketable securities (6/30/22)
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Experienced Management Team: Proven Track Records
Founding member
Jane Huang M.D.
Laurent Chardonnet
Chief Financial Officer
President and Chief
Medical Officer
Kris Vaddi, PhD
Founder &
Chief Executive Officer
Andrew Combs, PhD
Peggy Scherle, PhD
Executive Vice President
Chief Scientific Officer
and Head of Chemistry
Board of Directors
Paul Friedman, MD
CEO
Former CEO
Mardi Dier
CFO
Former CFO,
CBO
Victor Sandor, MD
Former CMO
David Bonita, MD
General Partner
Julian C. Baker
Managing Member
Baker Brothers Investments
Kris Vaddi, PhD
Founder &
Chief Executive Officer
Martin Babler
Former CEO
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Prelude Therapeutics Inc. published this content on 15 August 2022 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 15 August 2022 18:55:05 UTC.
Prelude Therapeutics Incorporated is a clinical-stage fully integrated oncology company built on a foundation of drug discovery to deliver novel precision cancer medicines to underserved patients. It has developed a diverse pipeline consisting of multiple distinct programs: kinases, targeted protein degraders, and precision antibody drug conjugates. Its product candidates include PRT3789, PRT2527 and PRT3645. PRT3789 is a highly selective degrader of SMARCA2 protein, which along with SMARCA4, controls gene regulation through chromatin remodeling. Its CDK9 program is an essential regulator of cancer-promoting transcriptional programs, including those driven by MCL1, MYC and MYB. PRT3645 is a brain and tissue penetrant molecule that potently targets CDK4/6 with a biased selectivity for CDK4. PRT2527 is designed to be a potent and selective CDK9 inhibitor. Its MCL1 candidate, PRT1419, is designed to be a potent and selective inhibitor of the anti-apoptotic protein, MCL1.