1. Multi-ModalityProbody® Therapeutic Pipeline to Address Major Unmet Needs in Oncology

First Quarter Earnings Update

May 8, 2024

© 2024 CytomX Therapeutics, Inc.

Forward-Looking Statements

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Today's Speakers

Dr. Sean McCarthy, D.Phil

Dr. Wayne Chu, M.D.

Chairman and CEO

Chief Medical Officer

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Agenda

Q1 2024 Updates & T-Cell Engager Strategy

Dr. Sean McCarthy, D.Phil. - Chairman and CEO

CX-904 Phase 1a study - Initial Dose Escalation Data

Dr. Wayne Chu, M.D. - Chief Medical Officer

Next Steps & Concluding Remarks

Dr. Sean McCarthy, D.Phil. - Chairman and CEO

Q&A Session

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Company Snapshot

Addressing Major Unmet Need in Oncology

PROBODY® Platform: Unique antibody masking strategy for tumor localization and enhancement of therapeutic index

Pipeline: >15 Probody programs in multiple therapeutic modalities; 3 clinical-stage molecules with retained commercial rights

Lead Programs: CX-904(EGFR-CD3),CX-2051 (EpCAM ADC), and CX-801(IFN-α2b)

Partners: Bristol Myers Squibb, Amgen, Astellas, Regeneron, Moderna

Financials: ~$150M cash balance as of Q1 2024 with cash runway to the end of 2025, excluding any potential milestones or new business development

Organization: ~120 employees; seasoned executive team with ~200 years of collective biotech experience; integrated R&D capabilities to support wholly-owned and collaboration programs

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CytomX Product Design Strategy Leverages the PROBODY® Platform

Optimized selection of target, prodomain and effector function

Optimized tuning of masking

to maximize potential

therapeutic index

Targets with validated efficacy andbroad anti-tumor potential that need localization to unlock potential

  • EGFR (CX-904)
  • EpCAM (CX-2051)

IFN-α(CX-801)

TARGET

Matching "effector"

to target to maximize

anti-cancer activity

T-Cell Engager

PRODOMAIN

EFFECTOR

ADC

Cytokine

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CytomX is Executing to Plan and Entering a Data-Rich Period

2024 & 2025 Potential Milestones

Program

Stage

2024

2025

Initial Phase 1a Dose Escalation data

CX-904

Phase 1 Dose

Additional Ph1a Update by end of 2024

Phase 1b Initiation

(EGFR TCE)

Escalation

Decision to Expand to Phase 1b in

Conjunction with Amgen

CX-2051

Phase 1 Dose

Phase 1 Initiation in EpCAM+ tumors

Initial Phase 1 Data in 1H 2025

(EpCAM ADC)

Escalation

including CRC in 1H 2024

Cleared First Escalation Cohort

CX-801

IND Cleared

Phase 1 Initiation in Solid Tumors

including Melanoma, RCC and HNSCC in

Initial Phase 1 Data

(Jan '24)

(IFNα2b)

1H 2024

Research

$10 million in Astellas milestones achieved in Q1 2024

Preclinical

More than 10 ongoing preclinical programs with partners; majority are TCEs

Collaborations

Additional research milestones achievable in 2024 - 2025 and beyond

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PROBODY® T-Cell Engager Strategy

© 2024 CytomX Therapeutics, Inc.

CytomX PROBODY® T-cell Engagers are Designed to Address Key Limitations of Conventional TCEs in Solid Tumors

PROBODY® T-Cell Engagers

Substrate linkers

Masks

  • Conventional T-Cellengagers are highly potent, but their use in solid tumors is significantly limited by:
    • Systemic toxicities such as Cytokine Release Syndrome (CRS) and ICANS
    • On-target,off-tumor toxicity
  • Masked, Conditionally activated Probody® T-Cell engagers are designed to retain potent anti-tumoractivity while having less systemic toxicities
  • CytomX has a broad pipeline of internal and partnered PROBODY® TCE programs with retained commercial rights on select programs, including CX-904 (EGFR-CD3)

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CX-904(EGFR-CD3) Builds on CytomX Scientific Leadership

Masking EGFR antibody therapeutics to widen therapeutic window

Science Translational Medicine, 2013

Cancer Research, 2022

Proof-of-concept that masking can reduce EFGR on-target toxicities

Proof-of-concept for efficacy and

therapeutic window for masked EGFRxCD3

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CytomX Therapeutics Inc. published this content on 08 May 2024 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 08 May 2024 23:20:10 UTC.