No insider purchase over the last 90 days. The latest was filed 21 Apr 2023.
Fate Therapeutics Inc, classified in the Healthcare & Pharma sector, is a listed company. Its insiders report their share dealings to SEC (Form 4). In the past year (18 October 2025 to 18 October 2026), 12 filings came from 6 insiders.
All open-market trades in the period are sales: 4 sales worth €103k, by 2 insiders, with no purchase on record. Biggest ticket of the year: €47k, sold by Valamehr Bahram and made public on 21 May 2026 (0.018% of market cap).
Filings reach the SEC (Form 4) feed a median of 1 day after the trade. Section 16 rules allow two business days to file each Form 4. Selling is not necessarily a view on the stock: liquidity needs and diversification are common motives.
For context, the typical company on the same exchange (median of 5,816 companies) published 19 filings over the same period, against 12 filings here. Since 2016, the database holds 2 purchases and 50 sales by insiders of the company. For the fiscal year to 31 December 2025, the annual 10-K puts revenue at 6.6 m USD and net income at -136.3 m USD.
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.
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 Fate Therapeutics Inc Buy (bullish), based on 9 analysts. Average price target: US$5.74.
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 132 declarations
Fate Therapeutics, Inc. is a United States biopharmaceutical company listed on NASDAQ and headquartered in San Diego, California (United States). Incorporated in Delaware in 2007, the company has built its identity around first-in-class, off-the-shelf cellular immunotherapies derived from human induced pluripotent stem cells (iPSCs). From an investor’s perspective, Fate is best understood as a platform company rather than a single-asset developer: its value proposition is tied to the ability to industrialize cell therapy manufacturing and broaden access beyond bespoke autologous treatments. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1434316/000095017025033510/fate-20241231.htm?utm_source=openai))
The company’s core technology is what it calls “cell programming.” Fate engineers human iPSCs with synthetic controls of cell function, creates clonal master cell lines, and then differentiates those lines into cellular therapy candidates. The strategic logic is clear: produce standardized, renewable starting material that can support scalable manufacturing and potentially improve consistency versus patient-specific cell therapies. The company also maintains office, laboratory, and GMP manufacturing space at its San Diego headquarters, underscoring its in-house development and manufacturing orientation. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1434316/000095017025033510/fate-20241231.htm?utm_source=openai))
Fate’s pipeline is centered on two major therapeutic areas: oncology and autoimmune disease. Its lead program, FT819, is a CD19-targeted CAR T-cell candidate developed from iPSCs and now focused primarily on autoimmune indications such as systemic lupus erythematosus and lupus nephritis. FT522 is an off-the-shelf CD19-targeted CAR NK cell candidate aimed at B cell–mediated autoimmune diseases, while FT836 is a next-generation CAR T program targeting MICA/B in solid tumors. This mix reflects Fate’s effort to create a differentiated portfolio spanning both hematology/autoimmunity and solid tumors. ([fatetherapeutics.com](https://www.fatetherapeutics.com/pipeline/?utm_source=openai))
Competitively, Fate stands out for its proprietary iPSC-based manufacturing platform. That differentiates it from conventional autologous CAR T companies and from allogeneic cell therapy developers relying on donor-derived starting material. The potential upside is a more scalable, accessible therapy model; the trade-off is that clinical and regulatory execution remains the dominant hurdle, and the sector is highly competitive and capital intensive. For equity investors, the investment case is therefore driven less by near-term revenue and more by clinical validation, partnering optionality, and proof that the platform can generate repeatable therapeutic results. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1434316/000095017025033510/fate-20241231.htm?utm_source=openai))
Recent developments have been encouraging from a pipeline-building standpoint. In 2024, the FDA allowed the IND for FT522 in certain B cell–mediated autoimmune diseases. In 2025, Fate reported that FT819 received RMAT designation from the FDA in moderate-to-severe systemic lupus erythematosus, while clinical work continued across FT819 and FT836. The company also disclosed that FT819 studies include sites in the United States, the United Kingdom, and the European Union, which broadens the program’s geographic footprint and signals a move toward more advanced clinical execution. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1434316/000095017025033510/fate-20241231.htm?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 | 6.6 m USD | -136.3 m USD | -1.15 USD | 10-K |
| Dec 2024 | 13.6 m USD | -186.3 m USD | -1.64 USD | 10-K |
| Dec 2023 | 63.5 m USD | -160.9 m USD | -1.64 USD | 10-K |
| Dec 2022 | 96.3 m USD | -281.7 m USD | -2.91 USD | 10-K |
| Dec 2021 | 55.8 m USD | -212.2 m USD | -2.24 USD | 10-K |
Amounts in USD, as filed (forms 10-K, 20-F or 40-F). Source: SEC EDGAR.