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Natera to Support New Clinical Trial Assessing ctDNA Dynamics with Latitude™ in Advanced Skin Cancers

Key Takeaway: Natera, Inc. has announced a collaboration for a Phase 1 clinical trial sponsored by Kupando Therapeutics. The trial will utilize Natera's Latitude assay to assess circulating tumor DNA dynamics in patients with advanced skin cancers. This partnership aims to enhance the understanding of molecular residual disease in the context of immunotherapy.

Market Sentiment Analysis

POSITIVE FACTORS

  • Natera collaborates on a significant Phase 1 clinical trial.
  • The trial focuses on advanced skin cancers, a critical area of research.
  • Natera's Latitude assay will contribute to precision medicine advancements.

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From our catalyst data and publicly available data · not financial advice
Cash runway
~43 mo
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Lead asset
Atezolizumab
Phase 3 · Muscle-invasive Bladder Cancer

Full Press Release Details

Phase I trial in Germany will support treatment response monitoring for Kupando Therapeutics’ investigational immunotherapy using Latitude MRD testing
AUSTIN, Texas--(BUSINESS WIRE)--Natera, Inc.(NASDAQ: NTRA), a global leader in cell-free DNA and precision medicine, today announced a new collaboration regarding a Phase 1 clinical trial, sponsored by Kupando Therapeutics.
Under the agreement, Natera’s Latitude tissue-free assay for molecular residual disease (MRD) detection will be used in Kupando’s clinical trial of its lead immunotherapy candidate, KUP-101. The trial will assess serial circulating tumor DNA (ctDNA) dynamics as part of treatment response monitoring. Patients with advanced tumors across multiple skin cancers will be treated with KUP-101 and Latitude MRD testing will be performed at multiple timepoints.
Following the successful dosing of the first patient, Kupando’s safety committee has approved the ongoing enrollment of further patients across the activated clinical sites, including leading oncology centers in Germany.
KUP-101 is designed to activate the innate immune system and induce trained immunity. It has potential as a tissue-agnostic treatment across multiple solid tumor types, both as a standalone therapy and in combination with other agents. To evaluate molecular response in this setting, the Latitude test is well suited to assess treatment response in the trial.
“Dosing our first patient is a defining inflection point in Kupando’s history,” said Johanna Holldack, M.D., founder and chief executive officer, Kupando Therapeutics. “By leveraging the power of innate immune stimulation and the induction of trained immunity, KUP-101 represents a fundamentally different way of approaching hard-to-treat cancers. Natera’s Latitude test can provide valuable insights into treatment response dynamics, helping us better understand the molecular activity of this novel therapeutic approach and advance our clinical development program for patients with advanced solid tumors.”
“We are pleased to work with Kupando as they advance this promising first-in-class approach to innate immune activation,” said Eric Matthews, general manager, biopharma, Natera. “Latitude’s capabilities make it ideally suited to evaluate ctDNA dynamics across diverse solid tumor types, and we look forward to generating molecular insights that can support Kupando’s development of KUP-101 and ultimately help patients with difficult-to-treat cancers.”

About Natera

Natera™ is a global leader in cell-free DNA and precision medicine, dedicated to oncology, women’s health, and organ health. We aim to make personalized genetic testing and diagnostics part of the standard-of-care to protect health and inform earlier, more targeted interventions that help lead to longer, healthier lives. Natera’s tests are supported by more than 400 peer-reviewed publications that demonstrate excellent performance. Natera operates ISO 13485-certified and CAP-accredited laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) in Austin, Texas, and San Carlos, California, and through Foresight Diagnostics, its subsidiary, operates an ISO 27001-certified and CAP-accredited laboratory certified under CLIA in Boulder, Colorado. For more information, visitwww.natera.com.

Forward-Looking Statements

All statements other than statements of historical facts contained in this press release are forward-looking statements and are not a representation that Natera’s plans, estimates, or expectations will be achieved. These forward-looking statements represent Natera’s expectations as of the date of this press release, and Natera disclaims any obligation to update the forward-looking statements. These forward-looking statements are subject to known and unknown risks and uncertainties that may cause actual results to differ materially, including with respect to our or our partners’ efforts to develop and commercialize new product offerings, whether the results of clinical or other studies will support the use of our product offerings, the impact of results of such studies, our expectations of the reliability, accuracy, and performance of our tests, or of the benefits of our tests and product offerings to patients, providers, and payers. Additional risks and uncertainties are discussed in greater detail in "Risk Factors" in Natera’s recent filings on Forms 10-K and 10-Q, and in other filings Natera makes with the SEC from time to time. These documents are available atwww.natera.com/investorsandwww.sec.gov.
Investor Relations: Mike Brophy, CFO, Natera, Inc.,investor@natera.comMedia: Lesley Bogdanow, VP of Corporate Communications, Natera, Inc.,pr@natera.com

Frequently Asked Questions

What is the focus of the new clinical trial?

The trial focuses on assessing circulating tumor DNA dynamics in advanced skin cancers.

Who is sponsoring the clinical trial?

The clinical trial is sponsored by Kupando Therapeutics.

What assay will Natera provide for the trial?

Natera will provide its Latitude tissue-free assay for molecular residual disease detection.

What is KUP-101?

KUP-101 is the lead immunotherapy candidate being tested in the clinical trial.

Last updated: Aug 12, 2026