Zymeworks Inc. · NASDAQ:ZYME

Zymeworks — Q3 2025 Earnings Presentation

16 slides from Zymeworks's earnings presentation, Nov 6, 2025

  1. Slide 1: 3Q 2025 Results Conference Call and Webcast

    3Q 2025 Results Conference Call and Webcast November 6, 2025 Nasdaq: ZYME | zymeworks.com

  2. Slide 2: Legal Disclaimer

    Legal Disclaimer This presentation and the accompanying oral commentary include “forward-looking statements” or information within the meaning of the applicable securities legislation, including Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of

  3. Slide 3: 3Q 2025 Earnings Results Call Agenda

    3Q 2025 Earnings Results Call Agenda Leone Patterson, MBA, CPA Sabeen Mekan, MD Paul Moore, Ph.D. Ken Galbraith EVP, CBO and CFO SVP Clinical Development CSO Chair and CEO • Business Update • Clinical Updates • R&D Update • Q&A • Financial Update • Q&A • Q&A • Q&A 3

  4. Slide 4: Financial Update

    FINANCIAL UPDATE Leone Patterson, MBA, CPA Executive Vice President, Chief Business and Financial Officer 4

  5. Slide 5: Continued Progress Across Business in Q3 2025

    Continued Progress Across Business in Q3 2025 Pipeline Partnership Financial Progress Progress Highlights • In October 2025, at EMSO our partner • J&J Innovative Medicine Initiated Progress on both clinical and preclinical Jazz presented a trial-in-progress poster Phase 3 study for pasritamig (JNJ-

  6. Slide 6: 3Q 2025 Revenues, Operating Expenses and Cash Resources

    3Q 2025 Revenues, Operating Expenses and Cash Resources Revenue Operating Expenses Cash, Cash equivalents and Royalty (USD) (USD) Marketable Securities (USD) Research support fee R&D & drug supply Milestones G&A $45.8M $333.4M $ 1.0 M $ 14.1 M $ 13.9 M $1.4 M $15.0M $324.2M $15.7M $ 324.2 M $34.4M $

  7. Slide 7: Clinical Development Update

    CLINICAL DEVELOPMENT UPDATE Sabeen Mekan, MD Senior Vice President, Clinical Development 7

  8. Slide 8: ZW191 Demonstrates a Favorable Clinical Safety Profile

    ZW191 Demonstrates a Favorable Clinical Safety Profile ZW191 ZW191 ZW191 ZW191 ZW191 ZW191 ZW191 Total TRAE, n (%) 1.6 mg/kg 3.2 mg/kg 4.8 mg/kg 6.4 mg/kg 8.0 mg/kg 9.6 mg/kg 11.2 mg/kg (n=41) (n=3) (n=3) (n=4) (n=10) (n=11) (n=8) (n=2) Any TRAE 1 (33) 3 (100) 3 (75) 8 (80) 10 (91) 6 (75) 2 (100) 33

  9. Slide 9: ZW191 Demonstrates a Potential Best-In-Class Efficacy Profile

    ZW191 Demonstrates a Potential Best-In-Class Efficacy Profile Best percent change in target lesion size from baseline (n=27) Preliminary efficacy for response-evaluable participants with gynecological cancer ZW191 ZW191 ZW191 ZW191 ZW191 ZW191 ZW191 Best 1.6 3.2 4.8 6.4 8.0 9.6 6.4-9.6 Total respons

  10. Slide 10: ZW191: Next Steps

    ZW191: Next Steps • Building confidence in our ADC platform through safety, Data-Driven pharmacokinetics, and efficacy with emerging clinical Development data • 11.2 mg/kg dose defined as MTD since this data-cut • Randomized dose optimization to begin in 4Q-2025 in Optimization & platinum resistant

  11. Slide 11: ZW251: Phase 1 Study in Glypican 3-Expressing HCC

    ZW251: Phase 1 Study in Glypican 3-Expressing Hepatocellular Carcinoma (HCC) (NCT07164313) Key Eligibility Criteria Part 1: Dose Escalation (~6 dose levels; n=60) Part 2: Dose Optimization (n=40) • HCC advanced or metastatic • Progressed on SOC treatment ZW251 ZW251 • Measurable by RECIST 1.1 ZW251

  12. Slide 12: Research & Development Update

    RESEARCH & DEVELOPMENT UPDATE Paul Moore, Ph.D. Chief Scientific Officer 12

  13. Slide 13: ZW191 Phase 1 Data Provides Early Validation of ADC Platform

    ZW191 Phase 1 Data Provides Early Validation of ADC Platform and Design Philosophy Clinical Assets Preclinical Assets Next Gen ZW191 ZW251 ZW220 ZW327 ZW318 Target FRα GPC3 NaPi2b Ly6E PTK7 Various Targeted small molecule, Novel Payload ZD06519 (TOPO1i) ZD06519 (TOPO1i) ZD06519 (TOPO1i) ZD06519 (TOP

  14. Slide 14: ZW171 Phase 1 Provides Learnings for Next-Gen T Cell Engager Pipeline

    ZW171 Phase 1 Provides Learnings for Next-Gen T Cell Engager Pipeline Molecular Design Clinical Design MSLN ZW171 MSLN Novel CD3 Azymetric QSP Modelling Target: MSLN x CD3 Subcutaneous Step Up CD3 Epitope and EFECT for FIH & Dose Format: T Cell Engager Delivery Dosing mutations Projections Strategy:

  15. Slide 15: Diverse Potential Revenue Streams from Existing Partnerships

    Diverse Potential Revenue Streams from Existing Partnerships • Near-Term Revenue Catalysts: Continued royalties from Jazz and BeOne Medicines for Ziihera® expected in 2025. • Long-Term Growth Potential: Wholly-owned assets provide flexibility for future licensing and royalty opportunities. Current P

  16. Slide 16: Q&A

    Q&A Ken Galbraith Chair & CEO Paul Moore, Ph.D. CSO Leone Patterson, MBA, CPA EVP, CBO and CFO Sabeen Mekan, MD SVP Clinical Development 16

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