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  • 7:45 am

  • Registration

  • 8:30 am

  • Co-Chair’s Opening Remarks

    Axel Hoos
    Axel Hoos, MD, PhD

    SVP, Oncology R&D, GSK

    Patrick Hwu
    Patrick Hwu, MD

    Head, Division of Cancer Medicine, Department Chair, Melanoma Medical Oncology Department Chair, Sarcoma Medical Oncology, MD Anderson Cancer Center

    Ian McCaffery new
    Ian McCaffery, PhD
    VP and Head of Oncology Translational Research, Janssen Research and Development

  • Preclinical Mechanistic Combinations Plenary Session

  • 8:45 am

  • IO Combinations with CAR-T Therapies

  • 9:05 am

  • Preclinical and Clinical Data on BiTE Platform and Associated Combos

  • 9:25 am

  • The Tumor Explant Model as a Model System to Understand Treatment Effects

    This talk will look at the infiltration of lymphocytes and cytokine/ chemokine profiles into the tumor and which drugs/drug combinations can drive that through a tumor explant model. This fully human, fully immunocompetent model system allows to monitor and understand the immediate effects of systemic treatments on the tumor and surrounding normal tissue.  This model to is used to identify mechanisms of response and resistance in tumor types.

  • 9:45 am

  • Model Systems for Studying Combinations

  • 10:05 am

  • Networking Break

  • 10:45 am

  • Single Cell Sequencing and Mechanisms of Immuno-Resistance

  • 11:05 am

  • Prioritizing Combinations using a Human Phenotypic Model for Drug Development

  • 11:25 am

  • Panel Discussion: Predicting IO Combination Success

    Predicting IO combination success does not have to wait until phase 3. This panel will address how do we predict what is going to work and what is not going to work by looking at model systems and early translational clinical trials.

  • 12:10 pm

  • Lunch

  • Translational Science & Emerging Biomarkers Plenary Session

  • 1:10 pm

  • IO Combinations Based on Tumor Mutation Analysis

  • 1:30 pm

  • Combinations Between Agents that Modulate the Microbiome and Checkpoints

  • 1:50 pm

  • Demystifying Tumor Immunogenomics: Key Challenges and Solutions

    Advances in immuno-oncology research have led to promising results with NGS-guided analysis for sensitive neoantigen identification as well as for the discovery of novel biomarkers. However, standard approaches suffer from limitations. Personalis addresses these issues using its proprietary ACE ImmunoID platform, which combines augmented exome and transcriptome sequencing with advanced analytics. We’ll share data that demonstrates the technical characteristics with an overview of the analytical validation, bioinformatics pipeline, neoantigen prediction and immunogenomics reporting capabilities.  Additionally, we will be sharing a case study demonstrating ACE ImmunoID’s further utility in biomarker discovery through identifying methods of tumor escape in patients treated with checkpoint modulators.

  • 2:10 pm

  • TCR Sequencing as a Predictive Biomarker of Response in IO

  • Operationalizing Combinations Plenary

  • 2:40 pm

  • Collaborations that Drive Combination Activities: The Science and Operations

    In this session, Merck clinical operation leaders address the operational considerations of combination studies. This includes:

    • What it takes to run combination studies from an operational standpoint
    • Creating drug sourcing activities, safety and quality agreements and with partnering pharma companies
    • Managing startup activities such as investigator brochures, risk language around combinations and a managing the safety along the way
    • Addressing drug procurement aspects and maintaining those quality aspects of bringing the combinations to the studies
  • 3:10 pm

  • Novel Platform Trial Design

    Novel-novel combinations platform trials offer the opportunity to efficiently evaluate and screen out for important new therapies in a standing clinical trials infrastructure. They also offer other efficiencies by use of statistical modeling to formally leverage both historical information and concurrent information in related populations. This talk will describe the various operational and statistical aspects of platform trials for novel-novel combinations in oncology.

  • 3:30 pm

  • Networking Break

  • 4:15 pm

  • Regulatory Framework for Investigating & Approving Combinations

    This talk will focus on the FDA guideline on novel-novel combinations and its application including existing approvals and future expectations.

  • 4:35 pm

  • Biomarker Procurement for IO Combinations

    The operational challenge that people still have regarding biomarkers is determining how you get material from patients that you can do analysis on and how do you standardize this? How do we get the biomarker questions answered that are at the heart of making combinations work?

  • 4:55 pm

  • Panel Discussion: The Operational Challenges of IO Combination Trials

    The complexities of doing combination clinical trials are huge. This panel will address:

    • How do you do clinical trials with different companies products?
    • How do you coordinate the supply chain with 2 drugs?
    • Who controls the rights? System processes? What are the thresholds?

  • IO Emerging Technologies & Innovative Solutions

  • 5:35 pm

  • This plenary will showcase companies that have technologies and solutions that will help stakeholders in the IO field advance combination developments to provide treatment for cancer patients.

  • 6:15 pm

  • Networking Reception


  • 8:15 am

  • Registration

  • 8:45 am

  • Co-Chair’s Opening Remarks

    Axel Hoos
    Axel Hoos, MD, PhD

    SVP, Oncology R&D, GSK

    Patrick Hwu, MD

    Head, Division of Cancer Medicine, Department Chair, Melanoma Medical Oncology Department Chair, Sarcoma Medical Oncology, MD Anderson Cancer Center

    Ian McCaffery new
    Ian McCaffery, PhD

    Vice President and Head of Oncology Translational Research, Janssen Research and Development

  • Clinical Combinations Plenary Session

  • 9:00 am

  • PD-1 Antibody Based Immuno-oncology Novel Combinations Across Indications

    After establishing PD-1 antibody monotherapy activity, enabled by precision medicine,  across multiple cancer types and lines of treatments study of combination therapies across multiple indications is suggesting significant promise. The data thus far suggest the PD-1 antibody is both broad spectrum across tumors and foundational to the combination approach. Novel combinations include those with standard therapies (e.g. chemotherapy), with targeted therapies, with other immune modulators and with tumor vaccines or oncolytic viruses.

  • 9:20 am

  • Immunotherapy Combinations with Parp Inhibitors

  • 9:40 am

  • Overcoming the Resistance to Immune Checkpoint inhibitors via Rational Combination of Immunotherapy

    • Preclinical studies to provide rationale for the combination Immunotherapy
    • Design and develop science-driven clinical studies of combination Immunotherapy
    • Biomarker analysis on the specimens from clinical trials of combination Immunotherapy
  • 10:00 am

  • Networking Break

  • 10:40 am

  • Perspectives on IDO Inhibition: Combinations Clinical Trial for Melanoma

    This talk will consist of two parts. The first part will look at the clinical data and full analysis on pembrolizumab in combination with epacadostat for Melanoma.  The second will address the mechanisms of why people thought it should work, why it has not and what can be learned moving forward.

  • 11:20 am

  • Novel Approaches to Engineered Cancer Immunotherapy

    In 2018, advances in therapeutic technologies are changing the options available for cancer immunotherapy. From engineered large molecules, to protein modification techniques, from cellular immunotherapy to personalized cancer vaccines, how we approach therapeutics is broader than ever. Objectives for engineered cancer immunotherapy approaches, techniques and emerging clinical data will be presented.

  • 11:40 am

  • Lymphocytes as a Drug for the Treatment of Metastatic Cancer

    In this talk, Dr Steven Rosenberg, Chief, Surgery Branch at the National Cancer Institute, will discuss cancer immunotherapy using the adoptive cell transfer of autologous lymphocytes with antitumor activity with an emphasis on the identification of T-cells that recognize the products of mutations unique to the individual patient’s cancer.

  • 12:00 pm

  • Update on IMPower150 in Lung Cancer

  • 12:20 pm

  • Panel Discussion: Addressing Combination Clinical Challenges

    This panel will discuss the clinical challenges with IO combinations and ways to move forward. Talking points include:

    • How do you identify patients who are in need of combination vs monotherapy?
    • Are combinations the approach to go and how do you select the right combination?
    • How do you identify patients who are likely to respond?
    • How do you identify genetic signature types to see mechanistically logical combinations?
    • What is the scalability of t-cell therapy?
    • How are we going to scale neo-antigen specific therapy if this is going to be novel to each patient?
    • How do we move forward?
  • 1:00 pm

  • Lunch

  • Business Aspects Plenary Session

  • 1:45 pm

  • Executive Fireside Chat: Partnership Deals and Combination Strategies

    Pharma and biotech executives come together on this fireside chat to share the nature of their partnership. They will address the partnership journey from the very start, what it encompassed and how it has evolved.

  • 2:15 pm

  • Panel: IO Combination Deals and Partnerships

    • What is the nature/landscape of the deals being done in combinations? (IO and non IO)
    • Who is doing them, what are they like, and are there any changes in the nature of the dealmaking that is occurring within IO because of the need for combinations?
    • Are the recent failures changing the nature of the partnering relationships? Is that changing the way people are thinking when it comes to funding at the early stage?
    • What is shaping the evolving nature or actual deal terms from the spectrum of collaboration through licensing to full sharing between biotech and pharma?
  • 3:00 pm

  • Afternoon Break

  • 3:15 pm

  • Panel: Investment Strategies Driving IO Combinations

    • What are the types of investments that will enable combinations? (ie: early mechanisms and novel platforms; pharma/biotech partnerships)
    • From an investment perspective, how do you identify what is coming up the pipeline? With all the combination studies out there, how do you get behind the right combination?
    • How do investors make the decision to invest in a seed round, series A of a novel mechanism or platform that is more likely to be useful in combination, or licensing assets?
    • Are we emphasizing too much on the adaptive immune system or should we look at innate immune system?
  • 4:00 pm

  • Panel: Assessing Value & Market Access Implications of Immuno-Oncology Combination Therapies

    • How do we think about the value?
    • How is the IO market access landscape evolving?
    • Where are we now in terms of payer management?
    • What is the impact of reimbursement challenges?
    • What does the future payer initiatives look like?
    • What pricing strategies/reimbursement models are there to help address the issues?
    • What can we demonstrate and communicate value to payers for optimal reimbursement/market access?
  • 4:45 pm

  • End of Conference