Conference Co-Hosts

University Of Michigan

2017 saw technology innovations, new therapies and diagnostics, value-based healthcare, and clinical protocol advancements as huge drivers, moving the needle from a one-size-fits-all model to personalized healthcare.

Some of the biggest impacts include:

  • Clearing CAR-T therapies for advanced lymphoma and Spark Therapeutics’ gene therapy for blindness by the FDA after decades of research
  • Foundation Medicine achieving FDA approval for its NGS-based FoundationOne genomic profiling cancer test, concurrent with the Centers for Medicare and Medicaid Services (CMS) issuing a preliminary national coverage determination for the test and others like it
  • Editing genes for gene therapy or controlling its expression via one of the most exciting innovations, the CRISPR-Cas9 technology, currently revolutionizing the field
  • Being able to understand and sequence complex DNA regions applying long-read technologies
  • Recognizing the importance of the microbiome and its impact on human health and translating learnings into therapies and diagnostics
  • New technologies such as liquid biopsy, cfDNA detection, and artificial intelligence/machine learning in genomics and drug discovery

The advancements were paradigm-shifting, especially when the different sectors of technology, research, healthcare, pharmaceutical, medical & equipment providers, and regulatory sectors converged.

On the technology side, big data analysis, artificial intelligence, and machine/deep learning made its mark with numerous applications in drug discovery, clinical diagnostics, and clinical trial optimization. With this rise, many companies are pushing the limits of disease understanding, diagnosis and therapy. Considering the need to automate and scale disease diagnosis, it has even been provocatively suggested that AI – once fully optimized and implemented – will one day replace human oncologists. While we see a huge uptick in AI/machine learning companies working feverishly on new solutions in this sector across the globe, we also hear doubt across the industry that AI is ready. Is it hype or reality? 2018 promises to provide insight and help clarify where we stand.

The CRISPR-Cas9 technology clearly dominated the research and applications sector promising the first set of its applications to enter clinical trials in 2018.

On the regulatory side, the FDA made strides with streamlining the development and review pathway for consumer tests that evaluate genetic health risks, approving Foundation Medicine’s FoundationOne CDx, Thermo Fisher Oncomine Dx Target Test, and Agilent’s GenetiSure Dx tests, while at the same time the FDA consumer advisory raised safety concerns related to the “Self-Administration” of illegal gene therapy products.

Medical and equipment providers continued with their delivery of powerful solutions that will impact the field of precision medicine, including Illumina’s NovaSeq, Oxford Nanopore’s GridION X5, or Mission Bio’s new Single-Cell DNA analysis platform Tapestri, to name a few.

The genetic testing sector is seeing a steady march forward with more companies providing a wider test spectrum. Color Genomics appears to be on a mission to democratize access to genetic testing via affordable and low cost cancer risk tests. The release of the Annual Report by UK Chief Medical Officer Dame Sally Davis provides evidence that genomics can improve health and prevent ill health. While this year saw a rise in testing coverages, some insurers worry about adverse selection and discrimination as the industry has not quite yet caught up with all the reimbursement demands and regulations that need to be put in place.

And then of course there is immunotherapy with its numerous successes including the newly developed CAR-T cell therapy, accompanied with Kyrmriah (Novartis) and Yescarta (Kite Pharma, now Gilead) approval, and Keytruda (Merck) becoming the first cancer treatment (anti-PD-1 immunotherapy) for (any) solid tumors based on a specific genomic profile. While the successes were celebrated, they also highlighted the new challenges of these drugs, including higher drug development process cost, and justification of the high overall therapy cost. Current Kyrmriah cost is $475K per treatment. The latter is a discussion point that the healthcare industry will surely need to address with all its stakeholders in mind as pressure from payors, advocacy groups, and providers are rising.

Astounding acquisitions (some of which went global) and massive financial investments occurred in 2017. The 1 billion dollar-valued company, GRAIL went global with the Cirina merger focusing on early cancer detection. Oxford Gene Technology was acquired by the Japanese in vitro diagnostics company Sysmex Corporation. At the same time, Invitae went on a shopping spree and acquired Ommodom’s CancerGene ConnectOn, Good Start Genetics, and CombiMatrix, focusing on enhancing their testing repertoire. Konica Minolta acquired Ambry Genetics in a $1 billion deal, and Gilead Sciences acquired Kite Pharma for $11.9 billion, again just to name a few examples. On the investment side, companies playing in artificial intelligence/machine learning (with Tempus, Sophia Genetics), digital health, and clinical genomics (Color Genomics, Counsyl, Edico Genome, Prenetics, WuXi NextCODE) seemed to be the big winners.

Last but not least, 2017 was also the year of more initiatives and large scale population studies including the new Big Data, Precision Medicine Network formed by five University of California precision medicine research centers, the recently launched Chinese Precision Medicine Initiative, the France Genome Medicine Plan, and the Precision Health at the University of Michigan Initiative, which – among other things – is focusing on opioid prescribing in the pre-surgical setting. For most studies, the aim is to better understand the link between genetics/specific genes and how they affect disease, while at the same time trying to integrate genomics for precision healthcare.

Given the paradigm shift, what better way is there than to ring in the New Year with the conference that highlights the latest significant developments changing the practice of medicine to personalized healthcare?

Be among the first to hear where the field is moving, what the next phase in this area of healthcare will look like, and how it will impact you and your business. PMWC 2018 has finalized a great lineup of speakers and representatives from 100,000 Genomics England, 23andMe, Agilent, Ambry Genetics, Foundation Medicine, GRAIL, Illumina, Invitae, Natera, Mission Bio, Oxford Nanopore, Thermo Fisher Scientific, and many more. Come join us for this information-rich gathering of the minds: it’s not too late!

Email [email protected] to inquire about being invited to the reception honoring Emmanuelle Charpentier (Max Plank Institute), Sir John Bell (Oxford University), Ronald Levy (Stanford), and Alan Ashworth (UCSF).

 

Happy New Year and Best Wishes for 2018 from the PMWC team!
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Interview with Gabriel Bien-Willner of Palmetto GBA

Q: What does your role entail as the director of the MolDX program at Palmetto GBA?

A: The job directing MolDX is multifaceted; first and foremost the MolDX program is responsible for assessing molecular diagnostic tests on the market and makes coverage and pricing determinations for such tests and technology. This is usually done through local coverage determination policies or technical assessments.

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Interview with Peter Marks of FDA

Q: The CBER’s Regenerative Medicine Advanced Therapy Designation program has been very successful, with about 100 requests for designation in the two years of its existence. Can you please tell us about the program and how it was put together?

A: The Regenerative Medicine Advanced Therapy (RMAT) Designation program came into being as part of the 21st Century Cures Act that was signed into law on December 13, 2016.

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Interview with Calum MacRae of Harvard Medical School

Q: What patient data do we need to better understand the underlying cause of disease and how to prevent it?

A: Medicine at present is highly underdetermined and data poor. To be precise, one must be comprehensive, so medicine (with our consent) will use not only what we currently conceive of as biomedical information, but also data from across our lives.

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Headlines from PMWC 2019 Silicon Valley

A big ‘Thank You’ to all of our presenters and attendees for celebrating 10 years of precision medicine progress with us! PMWC 2019 Silicon Valley was attended by 2000 participants from 35 countries, which included over 400 speakers in 5 parallel tracks!

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Interview with Ken Bloom of Ambry Genetics

Q: Tell us more about your organization/company. What patient population are you serving and which services are you specializing in?

A: Ambry Genetics is a recognized leader in high quality complex genetic testing. We seek to find the genomic cause or contributors to rare diseases, abnormal phenotypes and hereditary disorders.

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Interview with Lee Pierce of Sirius Computer Solutions

Q: What is the state of big data and analytics in healthcare, and how to best use the reams of data available?

A: More than ever, Healthcare organizations are achieving measurable value through use of their data and analytics assets. There is more raw material available than ever to create value. This raw material is the data flowing from internal systems and applications and also from devices and systems external to healthcare organizations.

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Interview with Anita Nelsen of PAREXEL

Q: There are various new, emerging technologies that bring us closer towards a cure for life-threatening disorders such as cancer, HIV, or Huntington’s disease. Prominent examples include the popular gene editing tool CRISPR or new and improved cell and gene therapies. By when can we expect these new technologies being part of routine clinical care?

A: Today’s emerging technologies are making the promise of individualized treatment a reality.

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Interview with Ilan Kirsch of Adaptive Biotechnologies

Q: The Nobel Prize in Medicine was awarded recently to James Allison and Tasuku Honjo for their work on unleashing the body’s immune system to attack cancer, a breakthrough that has led to an entirely new class of drugs and brought lasting remissions to many patients who had run out of options. The Nobel committee hailed their accomplishments as establishing “an entirely new principle for cancer therapy.” What is your first-hand experience the impact that those new drugs had on patients?

A: For decades cancer was viewed as solely a cell-autonomous condition.

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BMS buys Celgene | Lilly buys Loxo Oncology – Does this Signal a Return to Strong Deal-Making Activities in 2019?

Bristol-Myers Squibb’s blockbuster $74B deal to buy Celgene creates an oncology powerhouse amid industrywide excitement about the rapidly evolving science and explosive growth of the sector. The agreement could signal a return to deal-making for the pharmaceutical industry in the $133B global oncology therapeutics market.

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Interview with Gini Deshpande of NuMedii

Q: What need is NuMedii addressing?

A: NuMedii, has been pioneering the use of Big Data, artificial intelligence (AI) and systems biology since 2010 to accelerate the discovery of precision therapies to address high unmet medical needs. Artificial Intelligence approaches are a natural fit to harness Big Data as they provide a framework to ‘train’ computers to recognize patterns and sift through vast amounts of new and existing genomic

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Interview with Minnie Sarwal of UCSF

Q: Genomic medicine is entering more hospitals and bringing with it non-invasive technology that can be used to better target and treat diseases. What are some key milestones that contributed to this trend?

A: Completion of complete sequence data from the human genome project, and the advances in proteomic, microRNA and epigenetic assays added a layer of pathway biology to the understanding of human diseases.

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Interview with Shidong Jia of Predicine

Q: Once sequencing has been validated as a clinical solution via trusted workflows, and coinciding with the technological developments driving costs lower, we can expect accelerated human genome profiling for clinical Dx. How soon, do you think, will we see accelerated growth and what can we expect?

A: We will see accelerated human genome profiling for clinical Dx in 2019 and the coming years as more biomarker-based cancer drugs are gaining approval.

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Interview with Iya Khalil of GNS Healthcare

Q: Artificial intelligence (AI) techniques have sent vast waves across healthcare, even fueling an active discussion of whether AI doctors will eventually replace human physicians in the future. Do you believe that human physicians will be replaced by machines in the foreseeable future? What are your thoughts?

A: I think that there’s a lot of speculation and uncertainty around AI, but I don’t foresee a time when we won’t need physicians.

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Interview with Ilya Michael Rachman of Immix Biopharma Inc.

Q: The Nobel Price in Medicine was awarded recently to James Allison and Tasuku for their work on unleashing the body’s immune system to attack cancer, a breakthrough that has led to an entirely new class of drugs and brought lasting remissions to many patients who had run out of options. The Nobel committee hailed their accomplishments as establishing “an entirely new principle for cancer therapy.” Besides CAR T-cell therapy what do you think next generation immunotherapies will look like to successfully combat cancer?

A: The next generation of immunotherapies will build on the insights discovered by immunologists like James Allison and Tasuku Honjo and extend them to modify the body’s response to tumors.

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Join me to Kick off PMWC Silicon Valley in the Santa Clara Convention Center, Focusing on Every Element of Precision Medicine

My team worked in collaboration with Bill Dalton, Kim Blackwell, Atul Butte / India Hook Barnard, Nancy Davidson and Sharon Terry to create a program that touches every component of precision medicine while bringing together all of its key stakeholders. Leading participating institutions including Stanford Health Care, UCSF, Duke Health, Duke University, John Hopkins University, University of Michigan and more will share their learnings and experiences and their successes and challenges, as they make precision medicine the new standard of care for all.

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Johns Hopkins
University Of Michigan

The Precision Medicine World Conference (PMWC), in its 17th installment, will take place in the Santa Clara Convention Center (Silicon Valley) on January 21-24, 2020. The program will traverse innovative technologies, thriving initiatives, and clinical case studies that enable the translation of precision medicine into direct improvements in health care. Conference attendees will have an opportunity to learn first-hand about the latest developments and advancements in precision medicine and cutting-edge new strategies and solutions that are changing how patients are treated.

See 2019 Agenda highlights:

  • Five tracks will showcase sessions on the latest advancements in precision medicine which include, but are not limited to:
    • AI & Data Science Showcase
    • Clinical & Research Tools Showcase
    • Clinical Dx Showcase
    • Creating Clinical Value with Liquid Biopsy ctDNA, etc.
    • Digital Health/Health and Wellness
    • Digital Phenotyping
    • Diversity in Precision Medicine
    • Drug Development (PPPs)
    • Early Days of Life Sequencing
    • Emerging Technologies in PM
    • Emerging Therapeutic Showcase
    • FDA Efforts to Accelerate PM
    • Gene Editing
    • Genomic Profiling Showcase
    • Immunotherapy Sessions & Showcase
    • Implementation into Health Care Delivery
    • Large Scale Bio-data Resources to Support Drug Development (PPPs)
    • Microbial Profiling Showcase
    • Microbiome
    • Neoantigens
    • Next-Gen. Workforce of PM
    • Non-Clinical Services Showcase
    • Pharmacogenomics
    • Point-of Care Dx Platform
    • Precision Public Health
    • Rare Disease Diagnosis
    • Resilience
    • Robust Clinical Decision Support Tools
    • Wellness and Aging Showcase

See 2019 Agenda highlights:

    • Five tracks will showcase sessions on the latest advancements in precision medicine which include, but are not limited to:
      • AI & Data Science Showcase
      • Clinical & Research Tools Showcase
      • Clinical Dx Showcase
      • Creating Clinical Value with Liquid Biopsy ctDNA, etc.
      • Digital Health/Health and Wellness
      • Digital Phenotyping
      • Diversity in Precision Medicine
      • Drug Development (PPPs)
      • Early Days of Life Sequencing
      • Emerging Technologies in PM
      • Emerging Therapeutic Showcase
      • FDA Efforts to Accelerate PM
      • Gene Editing / CRISPR
      • Genomic Profiling Showcase
      • Immunotherapy Sessions & Showcase
      • Implementation into Health Care Delivery
      • Large Scale Bio-data Resources to Support Drug Development (PPPs)
      • Microbial Profiling Showcase
      • Microbiome
      • Neoantigens
      • Next-Gen. Workforce of PM
      • Non-Clinical Services Showcase
      • Pharmacogenomics
      • Point-of Care Dx Platform
      • Precision Public Health
      • Rare Disease Diagnosis
      • Resilience
      • Robust Clinical Decision Support Tools
      • Wellness and Aging Showcase
  • Luminary and Pioneer Awards, honoring individuals who contributed, and continue to contribute, to the field of Precision Medicine
  • 2000+ multidisciplinary attendees, from across the entire spectrum of healthcare, representing different types of companies, technologies, and medical centers with leadership roles in precision medicine
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