Adc Therapeutics Sa · NYSE:ADCT

Adc Therapeutics Sa — Q1 2024 Earnings Presentation

22 slides from Adc Therapeutics Sa's earnings presentation, May 6, 2024

  1. Slide 1: 1Q 2024 Earnings Call

    1Q 2024 Earnings Call May 6, 2024

  2. Slide 2: Agenda

    Agenda Ameet Mallik 01 Chief Executive Officer Business Update Pepe Carmona Financial Update 02 Chief Financial Officer Q&A Kristen Harrington-Smith Mohamed Zaki Chief Commercial Officer Chief Medical Officer 2

  3. Slide 3: Forward-Looking Statements

    Forward-Looking Statements This presentation and any accompanying oral presentation have been prepared by ADC Therapeutics SA ("ADC Therapeutics“, “we” or “us”) for informational purposes only and not for any other purpose. Nothing contained in this presentation is, or should be construed as, a reco

  4. Slide 4: Key Business Updates

    Key Business Updates § ZYNLONTA® 1Q 2024 net product sales of $17.8M, a 7% increase compared to 4Q 2023 Commercial Performance § Continued volume growth in the academic and community settings § LOTIS-7 cleared dose escalation; dose expansion underway with glofit combo in 2L+ DLBCL Pipeline § Initial

  5. Slide 5: Unlocking Potential Value of Robust ADC Portfolio

    Unlocking Potential Value of Robust ADC Portfolio Hematology Portfolio Solid Tumor Portfolio Short-Mid Term Mid-long Term ZYNLONTA ADCT-601 (AXL) § Maximize ZYNLONTA in 3L+ DLBCL § Optimizing dose for expansion as single agent and / or in combination in sarcoma, pancreatic, and NSCLC § Seek to expan

  6. Slide 6: Advancing ZYNLONTA Development in B-Cell Lymphomas

    Advancing ZYNLONTA Development in B-Cell Lymphomas Projected U.S. Market Value2, 2023 5-year prevalence3 DLBCL FL MZL^ Current Development Areas $3.1b2, ~109 K patients $2.6b2, ~61 K patients $1.4b2, ~38 K patients § LOTIS-5 and LOTIS-7 potential to move ZYNLONTA into 2L+ DLBCL Proportion of patient

  7. Slide 7: ZYNLONTA R/R MZL Opportunity Overview

    ZYNLONTA R/R MZL Opportunity Overview Phase 2 University of Miami IIT Initial Data Estimated 3 – 4 K 2L+ MZL patients are drug-treated in the US1; despite patients achieving durable responses, high unmet medical need remains with <30% CR for 2L+ NCCN preferred treatments2 2 FDA approved regimens (n

  8. Slide 8: Response Rates in Relapsed / Refractory MZL for Current NCCN Preferred Regimens

    Response Rates in Relapsed / Refractory MZL for Current NCCN Preferred Regimens with 2L+ Data NCCN Preferred^, FDA Approved Regimens NCCN Preferred Regimens^ CR PR CR PR 79% ORR 68% ORR 65% ORR 53% ORR 42% 36% 62% 40% 26% 29% 17% 13% 3 Zanubrutinib Zanubrutinib2 2 R2 R25 4 Benda * Obin1 Benda + + Ob

  9. Slide 9: A Phase 2, Open-label, IIT Evaluating Loncastuximab in R/R MZL

    A Phase 2, Open-label, IIT Evaluating Safety and Efficacy of Loncastuximab in R/R MZL Clinical Design Study Overview R/R MZL Previously Treated with ≥ 1 Line of Systemic § A multi-institutional study of 50 patients with r/r MZL after Therapy previous systemic treatment (clinicaltrials.gov ID: NCT052

  10. Slide 10: Patient Baseline Characteristics from Initial Data

    Patient Baseline Characteristics from Initial Data 15 evaluable patients out of 20 enrolled patients as of 04/18/2024 Baseline Characteristics N Previous Treatments N Number of patients 15 Non-systemic XRT 3 Splenectomy 1 Age, average (range), years 64 (48 – 80) Systemic Rituximab 6 Gender (M:F) 3:1

  11. Slide 11: Initial study results from University of Miami

    Initial study results from University of Miami presentation at Lymphoma Research Foundation’s 2024 MZL Scientific Workshop Data as of March 30, 2024 Initial Efficacy Findings § 13 out of 15 patients with a CR, 1 out of 15 with a PR PD Patient stopped due to a toxicity § 9 out of 13 CRs were achieved

  12. Slide 12: LOTIS-7 Part 1 Dose Escalation

    LOTIS-7 Part 1 Dose Escalation Data as of April 19, 2024 Initial Safety Findings CRS Profile § Majority of CRS events were grade 1 and no CRS > grade 2 was observed Arm E* (ZYNLONTA + Glofit) Arm F* (ZYNLONTA + Mosun) n=9 n=9 § All CRS grade 2 events responded to Tocilizumab / corticosteroids; no re

  13. Slide 13: Developing Differentiated ADCs with a High Therapeutic Index

    Developing Differentiated ADCs with a High Therapeutic Index A novel hydrophilic, highly stable, protease-cleavable linker conjugated to Exatecan NaPi2b Claudin-6 PSMA ASCT2 Target description Phosphate transporter Adhesion protein Enzymatic glycoprotein Amino acid transporter NSCLC NSCLC NSCLC Tumo

  14. Slide 14: 1Q 2024 Selected Financial Data

    1Q 2024 Selected Financial Data (in $ millions) Balance Sheet March 31, 2024 Cash and cash equivalents $234.3 GAAP Non-GAAP (Adjusted)* Statement of Operations 1Q 2024 % vs. 1Q 2023 1Q 2024 % vs. 1Q 2023 Product Revenues, Net 17.8 -5.8 17.8 -5.8 Research & Development Expenses 25.7 -32.9 26.3 -25.5

  15. Slide 15: Completed Registered Direct Offering of $105.0M

    Completed Registered Direct Offering of $105.0M § Priced a $105.0M underwritten offering, with 13,411,912 shares and 8,163,265 pre- funded warrants § Shares sold to investors at Friday closing price of $4.90 and pre-funded warrants sold at $4.81 (being the offering price per common share in the offe

  16. Slide 16: Corporate Business Development Strategy for ADCT Portfolio

    Corporate Business Development Strategy for ADCT Portfolio U.S. EX-U.S. HEMATOLOGY OVERLAND ZYNLONTA, ADCT-602 JOINT VENTURE Direct Partnership Business Development to Unlock Value SOLID TUMORS ADCT-601, Research Assets Co-development & Royalty & Co-promote* Milestones to ADCT Business Development G

  17. Slide 17: Delivering on Our Strategy

    Delivering on Our Strategy Milestones Achieved q LOTIS-7: Cleared dose escalation q r/r FL and r/r MZL IITs: Encouraging initial data shared q ADCT-601 (AXL): Dosing initiated in pancreatic q Research platform: Highlighted at Investor Event Upcoming Expected Milestones q ZYNLONTA q Achieve commercia

  18. Slide 18: 1Q 2024 Earnings Call

    Earnings Call . THERAPEUTICS Innovating Science. Inspiring Hope.

  19. Slide 19: Reconciliation of GAAP Measures to Non-GAAP Measures

    Reconciliation of GAAP Measures to Non-GAAP Measures Unaudited (in thousands, except for share and per share data) Three Months Ended March 31, (in thousands) 2024 2023 Change % Change Total operating expense $ (51,666) $ (69,202) $ 17,536 (25) % Adjustments: Share-based compensation expense (i) 158

  20. Slide 20: Current MZL Treatment Landscape

    Current MZL Treatment Landscape LoT / Epidemiology1 Treatment Paradigm2 3L+ # of treated patients T-cell-mediated therapy per year Anti-CD20-based regimens BTKis (Axi-cel) 0.8 – 1.3 K 2L # of treated patients per year Anti-CD20-based regimens BTKis 2.2 – 3.2 K 1L # of treated patients per year Anti-

  21. Slide 21: LOTIS-7 Part 1 Dose Escalation Grade 3 and 4 Adverse Events

    LOTIS 7 Part 1 Dose Escalation Grade 3 and 4 Adverse Events Regardless of relatedness, Data as of April 19, 2024 Arm E (Lonca + Glofit) Arm F (Lonca + Mosun) Total Patients Treated N=9 N=9 N=18 Patients with any grade AE 9 (100 %) 9 (100 %) 18 (100 %) Patients with Any Grade 3/4 AE 3 (33.3%) 5 (55.5

  22. Slide 22: LOTIS-7 Part 1 Dose Escalation Summary of Serious Adverse Events

    LOTIS 7 Part 1 Dose Escalation Summary of Serious Adverse Events Regardless of relatedness, Data as of April 19, 2024 Arm E (Lonca + Glofit) Arm F (Lonca + Mosun) Total Patients Treated N=9 N=9 N=18 Patients with any SAE 1 (5.5%) 5 (55.5%) 6 (33.3%) Cytokine release syndrome* 1 (5.5%) 4 (44.4%) 5 (2

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