Delivering the Potential of Immunotherapy
Corporate Overview
N o v e m b e r 2 0 2 1
NON-CONFIDENTIAL
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This presentation and the accompanying oral commentary contain forward-looking statements about us and our industry that involve substantial risks and uncertainties. All statements other than statements of historical facts contained in this presentation and the accompanying oral commentary, including statements regarding our future results of operations or financial condition, business strategy and plans and objectives of management for future operations, are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. In some cases, you can identify forward-looking statements because they contain words such as ''anticipate,'' ''continue,'' ''estimate,'' ''expect,'' ''may,'' ''plan,'' ''potential,'' ''predict,'' ''should,'' or ''will'' or the negative of
these words or other similar terms or expressions, although not all forward-looking statements contain these words. These forward-looking statements include, but are not limited to, statements concerning the following: the initiation, timing, progress and results of our research and development programs, preclinical studies, and clinical trials, including our Phase 1b trial of ATRC-101 and
development of ATRC-101, the development of ATRC-501, our EphA2 program and our other preclinical, clinical and regulatory plans, and the timing thereof; the availability and timing of data from monotherapy dose expansion cohorts in our Phase 1b trial of ATRC-101 and from combination cohorts evaluating ATRC-101 with pembrolizumab and with chemotherapy; continuing to build an infrastructure for the identification of targets; our potential product development opportunities for ATRC-501, trends consistent with the proposed MOA of innate immune system activation; development of a diagnostic to select participants based on target expression; our ability to identify and develop product candidates for treatment of additional disease indications; our expectations regarding the achievement and timing of research, development, clinical, regulatory and other corporate milestones, including our expected cash and the target IND filing for a second product candidate; and the implementation of our business model and strategic plans for our business, technologies, and current or potential future product candidates. You should not rely on forward-looking statements as predictions of future events. We have based the forward-looking statements contained in this presentation and the accompanying oral commentary primarily on our current expectations and projections about future events and trends that we believe may affect our business, financial condition and operating results. The outcome of the events described in these forward-looking statements is subject to
risks, uncertainties and other factors described in greater detail in our filings with the Securities and Exchange Commission (SEC) and available on the SEC's website at www.sec.gov, including in the "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" sections of our most recently filed annual report on Form 10-K and quarterly report on
Form 10-Q, and may cause our actual results, performance or achievement to differ materially and adversely from those anticipated or implied by our forward-looking statements. In addition, statements that "we believe" and similar statements reflect our beliefs and opinions on the relevant subject. These statements are based on information available to us as of the date of this presentation. While we believe that information provides a reasonable basis for these statements, that information may be limited or incomplete. Our statements should not be read to indicate that we have conducted an exhaustive inquiry into, or review of, all relevant information. These statements are inherently uncertain, and investors are cautioned not to unduly rely on these
statements. Moreover, we operate in a very competitive and rapidly changing environment. New risks and uncertainties emerge from time to time, and it is not possible for us to predict all risks and uncertainties that could have an impact on the forward-looking statements contained in this presentation and the accompanying oral commentary. The results, events and circumstances reflected in the forward-looking statements may not be achieved or occur, and actual results, events or circumstances could differ materially from those described in the forward-looking statements.
This presentation discusses our current and potential future product candidates that are under clinical investigation and which have not yet been approved for marketing by the U.S. Food and Drug Administration. No representation is made as to the safety or effectiveness of these current or potential future product candidates for the use for which such product candidates are being studied.
The forward-looking statements made in this presentation and the accompanying oral commentary relate only to events as of the date on which the statements are made, and while we believe such information forms a reasonable basis for such statements, such information may be limited or incomplete, and our statements should not be read to indicate that we have conducted an exhaustive inquiry into, or review of, all potentially available relevant information. We undertake no obligation to update any forward-looking statements made in this presentation and the accompanying oral commentary to reflect events or circumstances after the date of this presentation and the accompanying oral commentary or to reflect new information or the occurrence of unanticipated events, except as required by law. We may not actually achieve the plans, intentions or expectations disclosed in our forward-looking statements, and you should not place undue reliance on our forward-looking statements. Our forward-looking statements do not reflect the potential impact of any future acquisitions, mergers, dispositions, joint ventures or investments. We qualify all our forward-looking statements by these cautionary statements.
NON-CONFIDENTIAL | 2 |
Company Highlights
Discovering and Developing Novel Antibody-based Cancer Immunotherapeutics
Differentiated
Discovery
Approach
Large
Opportunities
Lead Candidate:
ATRC-101
- First-moveradvantages in accessing a potentially large and underexploited target space via interrogation of the human active anti-tumor immune response
- Delivers novel antibodies binding to targets otherwise unlikely discoverable by traditional approaches
- Scalable and industrialized platform
- Approach leads to antibodies that bind to "public" tumor targets
- Potential treatments for large patient populations across multiple tumor types
- Monoclonal antibody with a novel mechanism of action and target
- Demonstrated potent single-agentanti-tumor activity in multiple preclinical solid tumor models
- Disease control associated with target expression in first-in-human dose escalation study
- Combo study with PD-1 inhibitor enrolling patients, combo study with chemo planned for 2023
• Internal program targeting EphA2 progressing | ||||
Pipeline | • Collaborating with Xencor to develop T cell-engaging antibodies | |||
Expansion | • | Growing hit library of >2,000 human antibodies that bind to non-autologous tumor tissue preferentially | ||
• | ATRC-501: monoclonal antibody licensed to Gates Medical Research Institute for malaria prophylaxis | |||
NON-CONFIDENTIAL | 3 | |||
Pipeline
AssetTarget
ONCOLOGY
ATRC-101 | Novel RNP Complex |
APN-122597EphA2
MultipleMultiple
INFECTIOUS DISEASES
ATRC-501 / MAM01 | P. falciparum |
Circumsporozoite | |
(Malaria) | Protein |
APN-850271 | SARS-CoV-2 |
APN-906072 | |
Spike Protein | |
(COVID-19) | |
Format/MOA | Discovery | Lead / | Phase 1 Phase 2 | Collaborators |
Preclinical |
IgG Antibody w/ Driver
Antigen Engagement
Multiple Formats
Being Evaluated
- Cell Engagement
ADC (Cytotoxic) | + undisclosed |
Immunostimulation | + undisclosed |
Others |
IgG antibody
IgG antibody
ADC, antibody-drug conjugate; EphA2, ephrin type-A receptor 2; MOA, mechanism of action; RNP, ribonucleoprotein.
NON-CONFIDENTIAL | 4 |
The Atreca Discovery Platform
NON-CONFIDENTIAL | 5 |
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Atreca Inc. published this content on 08 November 2021 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 08 November 2021 02:17:04 UTC.