No insider purchase over the last 90 days. The latest was filed 07 Nov 2022.
This page follows insider dealings at Nuvalent, Inc. as filed with SEC (Form 4), a company from the Healthcare & Pharma sector. The last twelve months, up to 18 October 2026, brought 123 filings signed by 20 insiders.
All open-market trades in the period are sales: 38 sales worth €47.0M, by 8 insiders, with no purchase on record. Biggest ticket of the year: €30.8M, sold by Flynn James E and made public on 24 November 2025.
Compared with its exchange (5,816 companies, median 19 filings), a count of 123 filings is above the norm. Looking back to 2021, when coverage begins, insiders filed 2 purchases and 73 sales. On the fundamentals side, the SEC filing (10-K) for the period ending 31 December 2025 lists net income at -425.4 m USD.
Typically, a trade is published a median of 2 days after it takes place. US insiders must file a Form 4 within two business days of a trade. Sales are harder to read than purchases, since they often meet personal needs such as tax or diversification.
For comparison within the same sector, see the insider buying recorded at Cooper Companies, Inc. and Anixa Biosciences Inc. This summary is built from SEC (Form 4) disclosures alone and does not predict where the share price will go.
+3 other insiders
Entry is the close on the day after publication, the first price a reader could act on. Prices in the listing currency. Past moves are not a forecast.
Analysts rate Nuvalent, Inc. Hold (neutral), based on 9 analysts. Average price target: US$124.00.
This score ranks the purchase within its own market. A position size is suggested only on the venues of the backtested strategy universe; elsewhere, signals stay on watch. Not investment advice.
FY ended December 2025 · cache
25 of 311 declarations
Nuvalent, Inc. is a United States-based biopharmaceutical company listed on the NASDAQ under the ticker NUVL. Headquartered in Cambridge, Massachusetts, it is focused on precision oncology and, more specifically, on the development of highly selective kinase inhibitors for genetically defined subsets of non-small cell lung cancer (NSCLC). The company was founded in the early 2020s and has built its strategy around a relatively narrow but scientifically demanding thesis: design small molecules that can improve upon existing targeted therapies by addressing resistance, limiting off-target toxicity, and better penetrating the central nervous system. Nuvalent remains a clinical-stage company, so its value proposition is still driven primarily by pipeline execution rather than commercial sales. ([investors.nuvalent.com](https://investors.nuvalent.com/2026-04-07-Nuvalent-Announces-Submission-of-New-Drug-Application-to-FDA-for-Neladalkib-in-TKI-Pre-treated-Advanced-ALK-positive-NSCLC?utm_source=openai))
Its core pipeline is built around three main programs: zidesamtinib (NVL-520), a ROS1-selective inhibitor; neladalkib (NVL-655), an ALK-selective inhibitor; and NVL-330, a HER2-selective inhibitor. The company also has multiple discovery-stage research programs. From an investor perspective, this makes Nuvalent a focused oncology platform rather than a diversified pharmaceutical business. Its competitive position is based on structure-guided design and unusually high target selectivity, with the goal of serving patients whose disease has become resistant to prior kinase inhibitors or who need therapies with better tolerability and more durable responses. ([investors.nuvalent.com](https://investors.nuvalent.com/overview?utm_source=openai))
Nuvalent’s geographic footprint is concentrated in the United States, where its corporate base, clinical operations and investor relations functions are centered, although its trials and development programs are global in scope. The company’s recent news flow has been materially positive. On April 7, 2026, Nuvalent announced submission of an NDA to the U.S. FDA for neladalkib in TKI-pretreated advanced ALK-positive NSCLC, supported by data from the ALKOVE-1 phase 1/2 trial. In May 2026, the company also stated that zidesamtinib was under FDA review with a PDUFA target date, highlighting that at least two lead programs had advanced to late-stage regulatory inflection points. In addition, Nuvalent’s investor materials emphasize continued pipeline momentum and multiple expected milestones, which is important for assessing clinical and regulatory execution risk. ([investors.nuvalent.com](https://investors.nuvalent.com/2026-04-07-Nuvalent-Announces-Submission-of-New-Drug-Application-to-FDA-for-Neladalkib-in-TKI-Pre-treated-Advanced-ALK-positive-NSCLC?utm_source=openai))
Purchases our model currently ranks for the recommendations list.
All recommendations| Fiscal year end | Revenue | Net income | Diluted EPS | Filing |
|---|---|---|---|---|
| Dec 2025 | n.d. | -425.4 m USD | -5.85 USD | 10-K |
| Dec 2024 | n.d. | -260.8 m USD | -3.93 USD | 10-K |
| Dec 2023 | n.d. | -126.2 m USD | -2.17 USD | 10-K |
| Dec 2022 | n.d. | -81.9 m USD | -1.65 USD | 10-K |
| Dec 2021 | n.d. | -46.3 m USD | -2.13 USD | 10-K |
Amounts in USD, as filed (forms 10-K, 20-F or 40-F). Source: SEC EDGAR.