CORPORATE OVERVIEW: REINVENTING THERAPEUTIC ANTIBODIES FOR THE TREATMENT OF CANCER

Similar documents
Corporate Overview. June 2017

AbGn-107, an ADC Targets Gastrointestinal Tumors

INTERIM RESULTS AS OF MARCH 31, 2017

Second Quarter 2016 Financial Results. August 4, 2016

Second Quarter 2017 Financial Results. August 8, 2017

Corporate Presentation. April 2016

Axel Hoos, M.D., Ph.D., SVP, Therapeutic Area Head for Oncology R&D and Head of Immuno Oncology, GSK

First-in-Class Bispecific Antibodies For Cancer Immunotherapy

Preclinical to Clinical Translation of Antibody Drug Conjugates

leading the way in research & development

SORRENTO THERAPEUTICS, INC. (Exact Name of Registrant as Specified in its Charter)

Corporate Presentation. March 2018

Agios Pharmaceuticals, Inc. (Exact Name of Registrant as Specified in Charter)

S9 Implementation Working Group ICH S9 Guideline: Nonclinical Evaluation for Anticancer Pharmaceuticals Questions and Answers

Forward-looking statements

Unique PK-PD properties of biotechnology-based therapeutics [mabs] and First In Human dose considerations. [mabs -monoclonal antibodies ] Peter Lloyd

Nanotechnology: A Brief History and Its Convergence with Medicine. Weston Daniel, PhD Director of Program Management

Comparability Studies for Autologous Cell Therapy Products. Chris Shen July, 2017

SORRENTO THERAPEUTICS, INC. (Exact name of registrant as specified in its charter)

Momenta Pharmaceuticals Reports First Quarter 2017 Financial Results

TECHNOLOGIES & SERVICES FOR THERAPEUTIC ANTIBODY DEVELOPMENT

New Hope For Serious Infections

Antibody Targeted Amanitin Conjugates (ATACs) Expanding the ADC Landscape With a New Payload Targeting RNA Polymerase II

Creating Highly Efficacious ADCs for Low-Expression Targets While Improving Therapeutic Index TIM LOWINGER, PHD

Bank of America Merrill Lynch Healthcare Conference. September 13, 2013

Samatasvir (IDX719), a Potent Pan-Genotypic NS5A Inhibitor, for the Treatment of Hepatitis C Virus (HCV) Infection

Momenta Pharmaceuticals, Inc. 36 th Annual J.P. Morgan Healthcare Conference

ADVANCING SCIENTIFIC INNOVATION Together, the possibilities are endless.

MOLOGEN AG Quarterly Statement as at 31 March 2017 Contents 2

Management Discussion and Analysis for the Second quarter of FY

Citi s 2017 Global Healthcare Conference 6~7 December 2017, New York

Drug Development: Why Does it Cost so Much? Lewis J. Smith, MD Professor of Medicine Director, Center for Clinical Research Associate VP for Research

On Helix. 02 July Harren Jhoti President & CEO

DEVELOPING FIRST-IN-CLASS TREATMENTS IN HAEMATOLOGIC CANCERS

January (San Francisco, CA) January 8, 2018

Antisense Therapeutics Ltd ASX:ANP January 2017

Welcome to R&D Day! Christine Lindenboom VP, Investor Relations & Corporate Communications

Q4 and Full Year 2017 Conference Call. February 22, 2018

OnTarget September

INVESTOR PRESENTATION FULL YEAR 2007 RESULTS. February 2008

The science behind Betalutin : why is it unique? Roy H. Larsen PhD Sciencons AS, Oslo, Norway

Vecchi anticorpi per nuove terapie biologiche

OPT-302: a VEGF-C/VEGF-D Trap for wet AMD

Therapeutics. Corporate Presentation Henry Ji, PhD - President and CEO. 2015, Sorrento Therapeutics, Inc. ALL RIGHTS RESERVED.

Roche Committed to Innovation. Sal. Oppenheim European Healthcare Investors Conference Frankfurt, September 2, 2008

Development and Manufacture of a Novel Drug- Linker: Enabling High DAR ADCs. Michael J Kaufman, Ph.D. Senior Vice President, CMC

Bispecifics Hold Promise, but Awaiting Initial Data; Initiate at Equal-weight

Quantitative And Spatial Optimization Of Therapeutic Fusion Proteins

Oncology Dose-Finding Workshop Part 3

COMMITTEE FOR MEDICINAL PRODUCTS FOR HUMAN USE (CHMP)

DDI Assessment for Therapeutic Proteins and ADCs

The tetravalent bispecific NK-cell engaging antibody AFM13 (CD30/CD16A) engages and primes innate immune cells for anti-cancer immunity

Reviewers' comments: Reviewer #1 (Remarks to the Author):

Cancer ImmunoTherapy Accelerator (CITA) Dr Shalini Jadeja

1 st Quarter 2007 Earnings. April 19, 2007

Bench-to-Bedside Translation of ADCs using PK/PD M&S. Dhaval K. Shah, Ph.D.

Disclaimer. 2

Conference call transcript for the March 2017 Quarterly Report

ME-401: A Highly Differentiated PI3Kd- Selective Inhibitor

Pfizer Program in DMD. Beth Belluscio, MD-Ph.D. Pfizer Rare Disease September 9, 2017

GSK 916: anti-bcma ADC An exciting potential advance in the treatment of Multiple Myeloma

Polatuzumab vedotin A potent ADC in NHL

Investor Presentation Stellar Biotechnologies, Inc. Nasdaq: SBOT. February 7, 2018

Antibody Therapeutics: Challenges, Strategies and Innovations for the Next Generation

Spark Therapeutics, Inc. (Exact Name of Registrant as Specified in its Charter)

Recombinant Biglycan for the Treatment! of Duchenne Muscular Dystrophy!!! PPMD Annual Conference, Jun 2013! By Joel B. Braunstein, MD!

Intec. Pharma Unfolding drug delivery solutions. Investor Presentation. Nasdaq: NTEC. June 2017

CORPORATE NEWS EARNINGS PAION AG PUBLISHES GROUP QUARTERLY STATEMENT FOR THE FIRST NINE MONTHS OF 2016

Antibody Targeted Amanitin Conjugates (ATACs) Expanding the ADC Landscape With a New Payload Targeting RNA Polymerase II

Immunotherapy in Hemato-Oncology

INVESTOR PRESENTATION

February 28, Churchill Place Canary Wharf London E14 5EU United Kingdom

A Phase I/IIa Study of Human Anti-CD38 Antibody MOR03087 in Relapsed/Refractory Multiple Myeloma

File no./drug Name Name of firm/ Institute Recommendations. M/s. AstrazenecaPharma India Limited

Second Quarter 2017 Earnings Teleconference. August 1, 2017

Development of Multiplex Sensitive Anti-Drug Antibody Assays for CRISPR/Cas9 Gene Therapies

REVOLUTIONARY SCIENCE MEETS TRANSFORMATIVE CANCER THERAPY PHARMACY FELLOWSHIP PROGRAM

Regulatory Perspective

Regulatory Approval of Modern Gene-Based Cancer Immunotherapies CAR T Cells A product perspective

Assembly Biosciences Jefferies 2015 Microbiome Summit. December 16, 2015

First Annual Biomarker Symposium Quest Diagnostics Clinical Trials

Industry Academic Collaboration: A Key to Successful Involvement of Patients Early in Clinical Development

INTELLIGENT ANTIBODY DISCOVERY FROM HUMANS AND OTHER ANIMALS. Guy Cavet

Supplemental Financial Schedules May 19, 2015

A LentiVector Platform Company, and a leader in gene and cell therapy. Annual General Meeting 23 May 2017

Cellular Tumor Antigen P53 (Tumor Suppressor P53 or Antigen NY-CO-13) - Pipeline Review, H1 2016

Small-Cap Research. Atossa Genetics (ATOS-NASDAQ) ATOS: Zacks Company Report OUTLOOK

H.P. Grimm (1), F. Crameri (1), H. Hinton (2), D. Türck (1), H. Silber Baumann (1), B. Ribba (1)

The Promise and Challenge of Adaptive Design in Oncology Trials

"Stratification biomarkers in personalised medicine"

Investor Presentation. March 2018 (Nasdaq: PIRS)

DEVELOPING PRECISION THERAPIES IN HAEMATOLOGIC CANCERS

BIOMARKERS: TECHNOLOGIES AND GLOBAL MARKETS

Annual General Meeting KPMG Level 36, 727 Collins St Melbourne Tuesday 21 November am

What s the difference? Challenges in pre-clinical development of biologics

Transcription:

CORPORATE OVERVIEW: REINVENTING THERAPEUTIC ANTIBODIES FOR THE TREATMENT OF CANCER March 2018 2018 CytomX Therapeutics, Inc. 1

Forward Looking Statements Special Note Regarding Forward-Looking Statements This presentation may contain projections and other forward-looking statements regarding future events. All statements other than statements of historical facts contained in this presentation, including statements regarding our future financial condition, technology platform, development strategy, prospective products, preclinical and clinical pipeline and milestones, regulatory objectives, expected payments from and outcomes of collaborations, and likelihood of success, are forward-looking statements. Such statements are predictions only and involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These risks and uncertainties include, among others, the costs, timing and results of preclinical studies and clinical trials and other development activities; the uncertainties inherent in the initiation and enrollment of clinical trials; expectations of expanding on-going clinical trials; availability and timing of data from clinical trials; the unpredictability of the duration and results of regulatory review; market acceptance for approved products and innovative therapeutic treatments; competition; the potential not to receive partnership milestone, profit sharing or royalty payments; the possible impairment of, inability to obtain and costs of obtaining intellectual property rights; and possible safety or efficacy concerns, general business, financial and accounting risks and litigation. Because forwardlooking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified and some of which are beyond our control, you should not rely on these forward-looking statements as predictions of future events. More information concerning us and such risks and uncertainties is available on our website and in our press releases and in our public filings with the U.S. Securities and Exchange Commission. We are providing this information as of its date and do not undertake any obligation to update or revise it, whether as a result of new information, future events or circumstances or otherwise. Additional information may be available in press releases or other public announcements and public filings made after the date of this presentation. This presentation concerns products that have not yet been approved for marketing by the U.S. Food and Drug Administration (FDA). No representation is made as to their safety or effectiveness for the purposes for which they are being investigated. 2

Leveraging Our Innovative Probody Platform to Build a Pipeline of Differentiated Cancer Therapies Milestones Anticipated in 2018 Innovative Probody Platform Five clinical-stage programs by year end Furthest advanced programs remain wholly owned - CX-072 (anti-pd-l1): Initial clinical data mid-year - CX-2009 (CD166-directed PDC): Initial clinical data 2H 18 Strong partnered programs progressing well - BMS-986249 (anti-ctla-4): Phase 1/2 trial initiated - CX-2029 (CD71-directed PDC in co-development with AbbVie): IND filing 1H 18 Designed to enhance tumor targeting and create/widen therapeutic window Potential best-in-class immunotherapies against clinically-validated targets Potential first-in-class therapeutics against novel, difficult-to-drug targets Preclinical proof of concept achieved across ~15 targets in multiple modalities Validating Partnerships Partnerships with leading oncology players such as AbbVie, Amgen, BMS ~$400 million in upfront and milestone payments received to date Retained co-development rights and profit splits on certain products Well-Funded $374.1 million cash balance as of December 31, 2017 Funding into 2020 PROBODY is a trademark of CytomX Therapeutics, Inc. All other brands and trademarks referenced herein are the property of their respective owners. 3

Deep and Differentiated Probody Pipeline with Initial Data Read Outs Anticipated in 2018 PRODUCT CANDIDATE LEAD OPTIMIZATION IND-ENABLING PHASE 1/2 Commercial Rights CX-072 PD-L1 Probody CX-2009 CD166 Probody Drug Conjugate BMS-986249 CTLA-4 Probody CX-2029 CD71 Probody Drug Conjugate IND Anticipated in 1H 18 CX-188 PD-1 Probody IND Anticipated in 2H 18 T Cell Bispecific EGFR-CD3 Additional PDCs, IO, TCBs, Partners Immunotherapies Probody Drug Conjugates T Cell Engaging Bispecifics Multiple Programs 4

Probody Therapeutics are Designed to be Activated in the Tumor Microenvironment ANTI-CANCER ANTIBODY PROTEASES LINKER MASKING PEPTIDE 5

Preclinical Proof of Concept Achieved Across Multiple Modalities Immune Modulators/ Checkpoint Inhibitors Antibody Drug Conjugates T-Cell Bispecifics CARs PD-L1 (CX-072) PD-1 (CX-188) BMS-986249 CD166 (CX-2009) CD71 (CX-2029) EGFR-CD3 In Progress in Collaboration with MDACC Preclinical proof of concept achieved across ~15 targets 6

IMMUNO-ONCOLOGY PROGRAMS CX-072 (PD-L1) BMS-986249 (CTLA-4) 7

Full Potential for Combination Immunotherapy is Limited by Immune-Related Toxicities HYPOPHYSITIS * OCULAR TOXICITY DERMATITIS THYROIDITIS PNEUMONITIS HEPATITIS COLITIS, DIARRHEA THROMBOEMBOLIC NEUROPATHY Decreased Therapeutic Window with PD-L1/CTLA-4 Combination Absence of Therapeutic Window with PD-L1/BRAF Combination Melanoma Nivolumab Mono Ipilimumab Mono Nivo + Ipi Combo Melanoma Vemurafenib Mono Atezo + Vem Combo ORR 44% 19% 58% Grade 3 and 4 AEs* 16% 27% 55% Discontinued Drug 8% 15% 36% ORR (CR) 48% (1%) 67% (33%) Grade 3 and 4 AEs* 38% 67% Discontinued Drug NR** 100% Synergistic toxicity limits combo dosing More than 1/3 of patients unable to tolerate drug Compelling efficacy observed with PD-L1/BRAF combo 100% of patients unable to tolerate combination *Treatment-related **Not reported 1. Larkin et al., NEJM, July 2015. 2. Chapman et, al. NEJM, 2011. 3. Hamid, Society for Melanoma Research 2015 8

CX-072 as a Potential Centerpiece of Combination Cancer Therapy Kinase Inhibitors E.g. Zelboraf Checkpoint Inhibitors E.g. Yervoy ADCs Other Cancer Immunotherapies CX-072 PD-L1 PROBODY THERAPEUTIC Validated target Well-established efficacy & safety for class Probody Tx PDCs Pb-TCBs 9

PROCLAIM-072: Phase 1/2 CX-072 Assessment as Monotherapy and in Combination A1: DOSE ESCALATION 2017 2018 Inclusion: PD naïve, unselected cancer types Dose: 0.03 30 mg/kg A2: MANDATORY BIOPSY Inclusion: Selected for PD-L1 positivity Dose: 0.3 10 mg/kg B: IPILIMUMAB COMBO Inclusion: Unselected cancer types Dose: 0.3 30 mg/kg + IPI (3 and 10 mg/kg) C: VEMURAFENIB COMBO D: EXPANSION COHORT Inclusion: PD sensitive cancer Dose: TBA Inclusion: V600E BRAF mutated melanoma, PD-naïve Dose: 1 30 mg/kg + 960 mg VEM Enrollment completed Enrollment ongoing Initial Clinical Data Expected Mid-2018 10

2018 Clinical Goal: Preliminary Proof of Concept Antibody Protease Substrate Linker Mask Activation of Downstream Signaling Initial Safety Profile Presence of Target & Protease Activity Cleavage of Probody in Tumors Target Engagement by Probody Preliminary Anti-Tumor Activity Initial assessment to include: Probody PK, stability of mask in circulation Initial safety profile and anti-tumor activity as monotherapy and in combination Probody activation in tumor tissue Downstream biomarkers of activity 11

CX-072 Preclinical Proof of Concept TUMOR GROWTH SAFETY Induction of Autoimmunity Tx Similar Efficacy Autoimmunity Reduced Non-binding Parent PD-L1 CX-072 PD-L1 Control Antibody Antibody Probody Tx Tx Tumor Localizes to Tumor Prevents Binding in Periphery 12

Phase 1/2 Study of BMS-986249 (Probody of ipilimumab) 13

CTLA-4 Probody Tx Demonstrates Similar Efficacy with Improved Safety in Preclinical Studies Similar Anti-Tumor Efficacy Less Peripheral T-Cell Activation T u m o r V o lu m e (m m 3 /2 ) T u m o r V o lu m e (m m 3 /2 ) 2 0 0 0 1 5 0 0 1 0 0 0 5 0 0 0 0 1 0 2 0 3 0 4 0 5 0 D a y s P o s t Im p la n ta tio n 2 0 0 0 1 5 0 0 1 0 0 0 5 0 0 0 0 1 0 2 0 3 0 4 0 5 0 D a y s P o s t Im p la n ta tio n Control 0/10 Tumor Free Ipilimumab 7/10 Tumor Free Percentage of Ki-67+ CD4+ T-cells 50 45 40 35 3 0 25 20 15 10 5 0 Vehicle Anti-CTLA-4 (ipilimumab) Anti-CTLA-4- Probody-Tx Pretest Day 8 Day 15 Wider Safety Margin T u m o r V o lu m e (m m 3 /2 ) 2 0 0 0 1 5 0 0 1 0 0 0 5 0 0 0 0 1 0 2 0 3 0 4 0 5 0 D a y s P o s t Im p la n ta tio n Ipilimumab Pb Tx 6/10 Tumor Free HNSTD* in cynos 10 mg/kg ipilimumab 50 mg/kg ipilimumab Pb Tx In addition, ongoing collaboration on non-fucosylated version of CTLA-4 Probody Therapeutic * Highest non-severely toxic dose 14

PROBODY DRUG CONJUGATE PROGRAMS CX-2009 (CD166- DIRECTED PDC) CX-2029 (CD71- DIRECTED PDC) 15

Probody Technology Enables Selection of Better Antibody Drug Conjugate Targets ADC Targets are Limited Based on Healthy Tissue Expression: PDC Targets May Have More Attractive Attributes: Higher Expression Uniform Expression More patients More indications PDC Targets CD166 CD71 CD166 ADC Targets Her2 CD30 Mesothelin Her2 CD166 Folate Receptor Source: Human Protein Atlas 16

CX-2009: A Probody Drug Conjugate Targeting CD166 Preclinical Proof of Concept H 2 9 2 tu m o r m o d e l (N S C L C ) Protease DM4 Payload V1 V2 C1 C2 C3 CX2009 Antibody Substrate Linker Mask CD166 M e a n T u m o r V o lu m e (m m 3 ) 1 5 0 0 1 0 0 0 5 0 0 0 is o ty p e -D M 4 ; 5 m p k C D 1 6 6 P D C ; 5 m p k C D 1 6 6 A D C ; 5 m p k 0 1 0 2 0 3 0 s tu d y d a y Cancer Cell GLP Toxicity Study Results: Dosed up to 15 mg/kg in cynos Observed toxicity consistent with typical DM4 payload toxicity 17

PROCLAIM-CX-2009: CD166-Directed PDC Phase 1/2 Clinical Trial Design 2017 2018 A: DOSE ESCALATION Inclusion: 7 cancer types Dose: CX-2009 (0.25-6 mg/kg) A2: BIOPSY REQUIRED Inclusion: CD166+++ Dose: TBA B: COHORT EXPANSION(S) Enrollment ongoing Enrollment initiation in 2018 Inclusion: One or more of 7 cancer types Dose: TBA Seven CD166+ tumor types in monotherapy dose escalation arm: Breast cancer Castration-resistant prostate cancer Cholangiocarcinoma Endometrial cancer Head and neck cancer Non-small cell lung cancer Ovarian cancer Lung cancer Breast cancer Ovarian cancer Initial Clinical Data Expected 2H 2018 18

CD71 is a High Potential Target for a Probody Drug Conjugate Ubiquitously expressed on dividing, normal and malignant cells Mediates iron uptake required for cell division A professional internalizing protein: often used as a positive control in ADC experiments Expression in normal dividing cells prohibits development of a traditional ADC J. Cancer Ther. (2012) 19

Probody Platform Has the Potential to Enable CD71 as a Drug Conjugate Target PDC regresses tumors after a single dose PDC has efficacy across almost all preclinical models PDC opens therapeutic window where none previously existed Models tested 42 Regression or stasis 30 (71%) Growth inhibition 10 (24%) No response 2 (5%) Partnered with AbbVie: Co-development rights and profit split IND anticipated in 1H 2018 20

SUMMARY 21

Deep and Differentiated Probody Pipeline with Initial Data Read Outs Anticipated in 2018 PRODUCT CANDIDATE LEAD OPTIMIZATION IND-ENABLING PHASE 1/2 Commercial Rights CX-072 PD-L1 Probody CX-2009 CD166 Probody Drug Conjugate BMS-986249 CTLA-4 Probody CX-2029 CD71 Probody Drug Conjugate IND Anticipated in 1H 18 CX-188 PD-1 Probody IND Anticipated in 2H 18 T Cell Bispecific EGFR-CD3 Additional PDCs, IO, TCBs, Partners Immunotherapies Probody Drug Conjugates T Cell Engaging Bispecifics Multiple Programs 22

Alliances Have Brought Significant Capital into CytomX and Broadened Our Pipeline of Probody Therapeutics 10 oncology, 2 non-oncology targets CTLA-4 Probody Tx in Ph. 1 $287 million earned to date $4.8 billion in potential milestones, tiered royalties up to low-double digits CD71 (CX-2029) + 2 additional targets Co-development, cocommercialization, and profit split on CX-2029 IND on CX-2029 expected in 1H 2018 $45 million earned to date Up to $1B in potential milestones EGFR-TCB + 3 additional targets Co-development, profit split on EGFR-TCB $1.4B aggregated in potential development, regulatory & commercial milestones $60M earned to date CytomX receives rights to one Amgen preclinical TCB ~$400 million to date from pharma partnering Two partnered assets in the clinic in 2018 23

Strong Execution Throughout 2017 CX-072 (PD-L1) CX-2009 (CD166) CX-2029 (CD71) PROCLAIM-CX-072 ü Completed monotherapy dose escalation enrollment (Part A1) ü All combinations arms recruiting ü First monotherapy cohort expansion recruiting PROCLAIM-CX-2009 ü Monotherapy dose escalation recruiting ü Completed GLP toxicology studies ü $15M milestone received from AbbVie ü IND on track for 1H 18 CX-188 (PD-1) BMS-986249 (CTLA-4) Partnerships ü IND enabling studies initiated for 2H 18 filing ü Phase 1/2 recruiting ü Earned $10M milestone from BMS upon IND clearance ü BMS alliance expansion: $200M upfront ü Amgen co-development deal for T cell engaging Probody bispecifics: $40M cash, $20M equity purchase 24

Five Clinical-Stage Programs Anticipated by End of 2018 Milestones Expected in 2018 CX-072 initial clinical readout mid-year (wholly owned) CX-2009 initial clinical readout in 2H 18 (wholly owned) CX-2029 and CX-188 clinical initiation Well-Funded Strong cash position to advance pipeline Funding into 2020 Validating Pharma Partners Broad Probody Therapeutic Pipeline Poised for Proof of Well-Funded Concept and Value Creation 25

26