3 insiders bought €51k of shares over the last 90 days, the latest by Plott Ronald Todd, filed 30 Sept 2026.
Cluster: 3 buyers in 30 daysPhio Pharmaceuticals Corp. is a Healthcare & Pharma company. Its directors and officers file their transactions with SEC (Form 4). 7 insiders have disclosed 23 filings since 20 October 2025.
Only purchases show up on the open market, 12 purchases in all worth €79k, filed by 3 insiders. Buying on the open market means paying the going price with one's own funds, a different act from receiving shares as pay. The largest single trade was a purchase of €15k by Plott Ronald Todd, published on 20 August 2026, equal to 0.14% of the market capitalisation. Among those who bought: 2 senior executives and 1 chief executive.
Compared with its exchange (5,453 companies, median 22 filings), a count of 23 filings is above the norm. Looking back to 2017, when coverage begins, insiders filed 47 purchases and 4 sales.
In the case of 6 purchases, another manager of the company was buying within the same 30 days. When several insiders buy within a few weeks of each other, analysts speak of a cluster purchase. The latest purchase is recent: it was published 21 days ago, on 30 September 2026. Filings reach the SEC (Form 4) feed a median of 1 day after the trade. US insiders must file a Form 4 within two business days of a trade.
Every figure here comes from the filings published by SEC (Form 4) and describes the past, not future prices; it is not investment advice.
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.
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
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Phio Pharmaceuticals Corp. is a U.S.-listed biotechnology company trading on the NASDAQ market in the United States. It is focused on immuno-oncology drug discovery and development, built around its proprietary INTASYL™ platform, a self-delivering RNA interference technology designed to modulate disease-relevant gene expression without relying on conventional delivery systems. From an investor’s perspective, Phio remains a development-stage micro-cap biotech: it has no approved commercial product, limited operating history, and a valuation that is highly sensitive to clinical progress, intellectual property protection, and access to capital.
The company’s history traces back to Cutanea Life Sciences, which was founded by CEO Robert Bitterman; Phio later adopted its current name to reflect a strategic pivot toward cancer immunotherapy. According to its SEC filings, the company relocated its corporate headquarters from Marlborough, Massachusetts to King of Prussia, Pennsylvania, while maintaining a small laboratory presence in Worcester, Massachusetts. That move, together with broader cost rationalization efforts, underscores a lean operating model typical of early-stage biopharma companies.
Phio’s core business is concentrated on advancing product candidates derived from INTASYL. The company identifies PH-762 as its lead development compound and also references PH-894 as part of its pipeline. In preclinical work, INTASYL has been evaluated against multiple immune-oncology targets, including PD-1, BRD4, CTLA-4, TIGIT and CTGF. The company also emphasizes a sizeable patent estate for a company of its scale, with issued patents and patent families covering the INTASYL platform and related therapeutic uses. However, Phio is still reliant on third-party manufacturers for drug substance and clinical supply production.
In competitive terms, Phio operates in a crowded and rapidly evolving immuno-oncology field dominated by much larger pharmaceutical groups, venture-backed biotech peers, academic research institutions and other public and private developers. Its potential differentiation lies in the ease of incorporating INTASYL into existing cell-therapy workflows and in the platform’s self-delivering design. At the same time, the company faces the classic risks of an early clinical biotech: uncertain efficacy, safety and manufacturability, as well as a strong likelihood of future financing needs.
A key recent development was disclosed in Phio’s Form 10-Q for the quarter ended September 30, 2025. In July 2025, the company entered into a comprehensive drug substance development services agreement with a U.S. manufacturing partner to support analytical, process-development and cGMP manufacturing work for PH-762. This followed the termination of its clinical co-development arrangement with AgonOx and the wind-down of the associated Phase 1 study. For investors in France, Belgium or Switzerland, Phio is best viewed as a high-risk NASDAQ-listed healthcare story driven by platform validation, pipeline execution and financing discipline rather than near-term revenues.
| Fiscal year end | Revenue | Net income | Diluted EPS | Filing |
|---|---|---|---|---|
| Dec 2020 | n.d. | -8.8 m USD | n.d. | 10-K |
| Dec 2019 | 21,000 USD | -8.9 m USD | n.d. | 10-K |
| Dec 2018 | 138,000 USD | -7.4 m USD | n.d. | 10-K |
| Dec 2017 | 15,000 USD | -12.5 m USD | n.d. | 10-K |
| Dec 2016 | 19,000 USD | -9.0 m USD | n.d. | 10-K |
Amounts in USD, as filed (forms 10-K, 20-F or 40-F). Source: SEC EDGAR.