Track the Natera, Inc. share price and the full management transaction log of the company, a listed issuer based in United States. Shares are listed on the US market, under the authority of SEC (Form 4). Operating in the Healthcare & Pharma sector, Natera, Inc. has recorded 947 public disclosures. Market capitalisation: €48.8bn. The latest transaction was disclosed on 28 August 2026 (Attribution). Among the most active insiders: Sheena Jonathan. The full history is free.
Natera, Inc. has reported a total of 149 insider trading declarations in the last 90 days, with a total selling amount of approximately 67,219,878 euros and no buying activity. The top insiders include Sheena Jonathan, a Director, with sales totaling about 13,154,396 euros from 31 declarations, Daniel Rabinowitz, an Officer, with approximately 11,456,337 euros from 5 declarations, and Steven Leonard Chapman, the CEO and President, with around 9,836,188 euros from 23 declarations. Significant recent sales include Steven L Chapman selling approximately 7,827,480 euros on June 4, 2026, Daniel Rabinowitz selling about 6,947,142 euros on June 24, 2026, and Sheena Jonathan selling around 5,163,770 euros on August 7, 2026. Other notable sales were made by various insiders, including Gail Marcus and Herman Rosenman.
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Analysts rate Natera, Inc. Strong Buy (bullish), based on 21 analysts. Average price target: US$336.74.
This score ranks the purchase within its own market. No market currently meets the historical allocation criteria, so signals remain watch-only. Not investment advice.
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25 of 947 declarations
Natera, Inc. is a U.S.-based molecular diagnostics company listed on the NASDAQ under the ticker NTRA, in the United States. For international investors, the company is best understood as a precision-medicine leader built around cell-free DNA (cfDNA) testing, with a founding story that dates back to 2004 and a long-term mission to change standards of care in genetic disease. Its operational center is in Austin, Texas, while it also runs laboratories in San Carlos, California. Natera combines molecular biology, bioinformatics, and increasingly AI-enabled analytics to detect and interpret genetic signals from a blood sample. The business is organized around three major areas. In women’s health, Panorama is the company’s flagship non-invasive prenatal test, used to screen for common chromosomal conditions in pregnancy. In oncology, Signatera is the core growth and strategic platform: a tumor-informed minimal residual disease (MRD) assay used for cancer recurrence monitoring, treatment response assessment, and longitudinal disease management. In organ health, Prospera supports transplant rejection surveillance, while Renasight addresses genetic causes of chronic kidney disease. This portfolio gives Natera exposure to multiple high-value clinical workflows rather than a single diagnostic niche. From a competitive standpoint, Natera positions itself as one of the leading cfDNA diagnostics companies, with differentiation based on assay design, clinical evidence, and an extensive publication record. The company highlights the strength of its validation studies, broad clinical utility, and the depth of its data assets. That said, the commercial footprint is still overwhelmingly U.S.-centric: international revenue remains relatively small, so reimbursement trends, physician adoption, and payer coverage in the United States are especially important to the investment case. Recent developments underscore the company’s momentum. On May 7, 2026, Natera reported first-quarter 2026 revenue of $696.6 million, up 38.8% year over year, supported by continued test volume growth, including strong oncology growth. During 2025 and early 2026, the company acquired Foresight Diagnostics, launched proprietary AI foundation models to speed diagnostic and therapeutic innovation, and secured an FDA approval for Signatera CDx in muscle-invasive bladder cancer. Natera therefore offers investors a growth-oriented healthcare diagnostics story with meaningful clinical optionality, but also with execution risk, heavy R&D intensity, and continued dependence on U.S. market adoption.