
The importance of truncal somatic mutations in MRD testing
Haystack MRD™ prioritizes truncal somatic mutations—those mutations that are present at the initial formation of a tumor, or the trunk of the cancer evolutionary tree.
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Haystack MRD™ prioritizes truncal somatic mutations—those mutations that are present at the initial formation of a tumor, or the trunk of the cancer evolutionary tree.
One of the most critical differentiators among minimal residual disease (MRD) tests is whether they are tumor-informed or whether they are tumor-naive.
The landmark DYNAMIC study is the first prospective, randomized, interventional trial to demonstrate the clinical benefit of MRD testing to guide adjuvant therapy
Haystack MRD™ strikes the right balance of DNA molecules interrogated and number of mutations tracked for optimizing test efficiency and sustainability
Chris is a seasoned regulatory professional with a strong track record in the diagnostics industry. Her expertise has played a pivotal role in ensuring the successful registration and commercialization of a diverse array of products, including Companion Diagnostics, both in domestic and international markets.
In her role as Sr. Director of Regulatory Affairs at Haystack Oncology, Chris focuses on ensuring adherence to all pertinent regulations, fostering the safe and effective development of our product portfolio.
Throughout her career, Chris has made significant contributions at leading organizations such as Resolution Bioscience, Nanostring Technologies, and Roche Tissue Diagnostics, where her regulatory input significantly influenced the development, approval, and market launch of groundbreaking products in the field.
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Tweed Hanusek heads up Quality Assurance at Haystack and brings extensive experience developing, implementing, and improving quality system policies in accordance with applicable regulations. Prior to joining Haystack, Tweed held various quality leadership roles where he rebuilt global quality organizations to achieve compliance while also ensuring sustainability. Throughout his career, Tweed has successfully managed regulatory inspections, developed remediation strategies, and developed global strategic quality initiatives to achieve compliance and support business growth.
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Giulia, the Associate Director of Translational Science at Haystack Oncology, plays a vital role on the product development team, supporting clinical development, biopharma, and R&D efforts. Throughout her entire career, she has been dedicated to advancing the field of oncology through her expertise in analyzing circulating free DNA. Giulia boasts a portfolio of over 60 co-authored publications, with a focus on liquid biopsy and oncology, specifically delving into the molecular underpinnings of drug resistance and genomic evolution in cancer. Holding a Ph.D. in Molecular Medicine from The University of Turin (Italy), her true passion lies in assisting clinicians with real-time cancer patient monitoring and providing guidance for the most effective treatment strategies.
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Joel has overseen financial and business operations for multiple life sciences companies. Most recently, he served as Vice President of Finance & Corporate Development at Sema4, an AI-focused precision medicine company. Previously, Mr. Kaufman served as Chief Business Officer, at Navidea Biopharmaceuticals. He also served as an Equity Research Analyst at Goldman Sachs covering the Life Science Tools, Diagnostics, and Medical Technology sectors. Mr. Kaufman holds an MBA from Northwestern University’s Kellogg School of Management and a BA from the University of Pennsylvania.
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Jen serves as the Senior Director of Pharma Partnering and Strategic Alliances at Haystack Oncology, where she facilitates key collaborations to bring the promise of precision medicine closer to patients. Jen has a background in law, as well as oncology diagnostics and drug development, previously serving in roles at Sysmex Inostics, Natera, and PGDx/Labcorp. Leading with the philosophy that a culture of collaboration is the path forward to improving cancer patient care, Jen engages closely with pharma and healthcare systems to support their research and clinical development programs. Jen holds degrees from Georgetown University and Suffolk University Law School and has over a decade of experience in operations and business development.
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