15/02/2022 - Adaptive Biotechnologies Corporation: Adaptive Biotechnologies Q4 2021 Earnings Presentation

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Adaptive biotechnologies q4 2021 earnings presentation

Fourth Quarter and FY 2021

Earnings Conference Call

Safe Harbor

This presentation has been prepared by Adaptive Biotechnologies Corporation ("we," "us," "our," "Adaptive" or the "Company") and is made for informational purposes only. The

information set forth herein does not purport to be complete or to contain all relevant information. Statements contained herein are made as of the date of this presentation unless stated otherwise. This presentation shall not constitute an offer to sell or the solicitation of an offer to buy securities, nor shall there be any sale of these securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction.

This presentation contains "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements are intended to be covered by the "safe harbor" created by those sections. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based on our current beliefs, expectations and assumptions regarding the future of our business, future plans and strategies, our development plans, our preclinical and clinical results and other future conditions. In some cases, you can identify forward-looking statements by the following words: "may," "will," "could," "would," "should," "expect," "intend," "plan," "anticipate," "believe," "estimate," "predict," "project," "potential," "continue," "ongoing" or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words. All statements, other than statements of historical facts, contained in this presentation are forward looking statements, including statements regarding the ability to map adaptive immune responses to various disease states, including T cell responses to COVID-19 or other infectious diseases, as well as autoimmune disorders and cancer, the ability to leverage any such findings to advance solutions to diagnose, treat and prevent infectious diseases or other diseases; regarding our future financial or business performance, conditions, plans, prospects, trends or strategies and other financial and business matters; our current and prospective products and product candidates, including clonoSEQ, immunoSEQ T-MAP COVID and T-Detect products, planned non-IDE clinical studies, clinical trials and preclinical activities, research and development costs, current and prospective collaborations, including our collaboration with Genentech, the estimated size of the market for our products and product candidates; the timing and success of our development and commercialization of our current and anticipated product candidates and the expansion of existing product lines such as T-Detect into additional indications; the availability and extent of reimbursement coverage by government and private payors; the availability of alternative therapies for our target markets; and the other risks and uncertainties described in our filings with the Securities and Exchange Commission including the Risk Factors and Management's Discussion and Analysis of Financial Condition and Results of Operations sections of our Annual Report on Form 10-K filed on February 15, 2022. 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. Risks and uncertainties could cause actual results to differ materially from those expressed in our forward-looking statements. Accordingly, readers are cautioned not to place undue reliance on these forward-looking statements. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein.

Certain information contained in this presentation relates to or is based on studies, publications, surveys and other data obtained from third-party sources and the Company's own internal estimates and research. While the Company believes these third-party sources to be reliable as of the date of this presentation, it has not independently verified, and makes no representation as to the adequacy, fairness, accuracy or completeness of, any information obtained from third-party sources. In addition, all of the market data included in this presentation involves a number of assumptions and limitations, and there can be no guarantee as to the accuracy or reliability of such assumptions. Finally, while we believe our own internal research is reliable, such research has not been verified by any independent source.

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Business areas of focus going forward

MRD

Immune Medicine

Driven by clonoSEQ/MRD assay applications

Driven by immune receptor data opportunities

TAM ~$6B1

TAM ~$48B2

Drug

Discovery

Clinical

MRD

Clinical

Pharma

Cell Therapy

Testing

Pharma

Testing

Services

Vaccines

1. Global TAM: $4.5B clonoSEQ clinical testing; $1.5B Pharma partnerships (including

2. Global TAM: illustrative TAM for 3 indications for T-Detect (one infectious disease,

regulatory milestones)

one autoimmune disease, one oncology) and drug discovery in cell therapy oncology

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Key Achievements through 2021

MRD Business

  • Key data read outs demonstrating clinical utility
  • Expanded commercial team, added product line enhancements for CLL patients
  • Signed 2 significant pan-portfolio MRD partnerships across all heme indications
  • Recognized $10M in milestones from pharma partners

Strong RevenuesImmune Medicine Business

FY'21 $154.3M (+57% y/y)

Q4'21 $37.9M (+26% y/y)

Genentech selected TCR candidate targeting a shared cancer neoantigen Successfully completed initial POC screens for personalized product

Extended platform to vaccines with Nykode collaboration; phase 1/2 enrolling T-Detect COVID: granted EUA by the FDA with >30k tests ordered

Completed first T-Detect clinical validation study with ImmuneSense Lyme Identified multiple T-Detect signals in autoimmune disorders

T-MAP COVID agreements with partners including J&J, AZ, Moderna

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Our MRD Heme business: synergistic value of pharma and clinical diagnostic

Tests Delivered '21

  • Q4: 6,356 (+7% vs Q3)
  • FY: 22,516 (+48% Y/Y)

MRD

Ordering HCPs

• 1,735 (+57% Y/Y)

Clinical Testing

Pharma Trials

Ordering Accounts

  • 372 (+32% Y/Y)
  • 60 Companies

155 Active trials

  • $330M Milestones

Embedded as clinical

endpoint across multiple

drug modalities and

diseases

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Disclaimer

Adaptive Biotechnologies Corporation published this content on 15 February 2022 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 15 February 2022 22:00:23 UTC.

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