Welcome to our dedicated page for Prelude Therapeutics SEC filings (Ticker: PRLD), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Parsing a biotech filing loaded with clinical data tables and dilution clauses can feel impossible. Prelude Therapeutics’ precision-oncology focus means every 10-K includes pages on SMARCA2 degrader chemistry, while each 8-K may reveal pivotal trial readouts that move the stock overnight. If you have ever hunted for cash-runway details or wondered whether a secondary offering is hiding in the footnotes, you know how complex Prelude’s disclosures can be.
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Looking for actionable insights? Compare segments with our Prelude Therapeutics earnings report filing analysis. Review executive pay in the Prelude Therapeutics proxy statement executive compensation section, or see confidence signals via Prelude Therapeutics executive stock transactions Form 4. We even decode material news with Prelude Therapeutics 8-K material events explained and offer a Prelude Therapeutics annual report 10-K simplified readout so you can spot clinical milestones, partnership terms and dilution risks in minutes—not hours.
Prelude Therapeutics (PRLD) filed its Q3 2025 10‑Q, reporting revenue of $6.5 million from an amended AbCellera collaboration, total operating expenses of $26.9 million, and a net loss of $19.7 million ($0.26 per share). Cash, cash equivalents, restricted cash and marketable securities were $58.2 million as of September 30, 2025.
Subsequent to quarter‑end, the company received $6 million from an expanded AbCellera agreement and $60 million in capital from Incyte (an initial $35 million in cash plus a $25 million equity investment at $4.00 per share for 6,250,000 non‑voting shares). As of November 10, 2025, 62,865,270 voting and non‑voting common shares were outstanding. Based on preliminary estimates, these funds and existing balances could extend cash runway into 2027; however, the company states that substantial doubt exists about its ability to continue as a going concern.
Management announced a pause of the SMARCA2 degrader program, an ~11% workforce reduction with $0.5 million in one‑time costs, and noted regained compliance with Nasdaq’s $1.00 minimum bid price requirement. Year‑to‑date operating cash use was $79.4 million, partially offset by $113.8 million provided by investing activities from marketable securities maturities.
Prelude Therapeutics (PRLD) furnished an 8-K announcing it issued a press release with financial results for the three months ended September 30, 2025. The press release is provided as Exhibit 99.1, and an investor presentation intended for use by management is included as Exhibit 99.2. The materials are being furnished under Items 2.02 and 7.01 and are not deemed filed or incorporated by reference under the Exchange Act. The filing was signed by Chief Legal Officer, Corporate Secretary, and Chief Financial Officer Bryant Lim.
Prelude Therapeutics (PRLD) reported a director equity grant. On 11/05/2025, the reporting person received stock options for 121,285 shares at an exercise price of $1.39 per share. The options vest over one year, at one‑twelfth each month, and expire on 11/04/2035. The filing was made by one reporting person with direct ownership.
Prelude Therapeutics (PRLD) announced an Exclusive Option Agreement with Incyte for its selective JAK2V617F JH2 inhibitor program in myeloproliferative neoplasms. The deal delivers $60 million in capital upfront, comprising $35 million in cash and a $25 million equity investment.
Incyte may exercise its option to acquire the program for $100 million during the defined Option Period, with up to $775 million in additional clinical and regulatory milestones and single-digit royalties, bringing total potential cash payments to up to $910 million. Concurrently, Incyte agreed to purchase 6,250,000 non‑voting shares at $4.00 per share, with registration rights for resale on a Form S‑3 after closing. Prelude plans to use proceeds to advance its pipeline, including KAT6A and JAK2V617F, and for general purposes. The company also reported leadership changes—its President and CMO, Jane Huang, M.D., resigned and will serve as a consultant—and a pause of clinical development for its first‑in‑class SMARCA2 degrader as part of a strategic portfolio shift.
Prelude Therapeutics (PRLD) reported an insider equity grant on a Form 4. On 10/17/2025, a director received 76,000 director stock options at an exercise price of $1.19 per share, expiring on 10/16/2035.
The award vests over three years at one‑thirty‑sixth per month, subject to continued service. Following the transaction, the reporting person beneficially owned 76,000 derivative securities, held directly.
Prelude Therapeutics (PRLD) reported an insider filing: a Form 3 initial statement of beneficial ownership tied to an event on 10/17/2025.
The filing identifies the reporting person as a Director and states in the remarks that no securities are beneficially owned. It was filed by one reporting person and signed by /s/ Bryant D. Lim, Attorney-in-Fact pursuant to an Exhibit 24 Power of Attorney. This sets the insider’s baseline ownership as of the reported date.
Prelude Therapeutics announced a Board transition. Mardi Dier, a Class III director, notified the Company of her resignation effective
Effective the same date, the Board appointed Katina Dorton, J.D., MBA as a Class III director and named her Chair of the Audit Committee. She will serve until the 2026 Annual Meeting of Stockholders and until a successor is elected and qualified. In line with director compensation policy, Ms. Dorton received non-incentive stock options to purchase up to 76,000 shares, vesting one‑thirty‑sixth monthly over three years, subject to continued service. The Company furnished a press release as Exhibit 99.1.
Jane Huang, President and CMO of Prelude Therapeutics Inc (PRLD), reported transactions on
Prelude Therapeutics reported continued operating losses while advancing multiple oncology programs and managing liquidity constraints. For the six months ended June 30, 2025, the company recorded a $63.3 million net loss and had an accumulated deficit of $646.9 million. At June 30, 2025, cash, cash equivalents, restricted cash and marketable securities totaled $77.3 million, but management states these funds are insufficient to cover at least the next twelve months absent additional financing, and substantial doubt exists about the company’s ability to continue as a going concern.
Operationally, R&D and G&A decreased year-over-year to $54.6 million and $12.2 million for the six months, respectively, as clinical expenses and stock-based compensation moderated. Key program milestones include ongoing Phase 1/2 activity for SMARCA2 degraders (PRT3789 and oral PRT7732) and collaborations with AbCellera and Merck. The company also received a Nasdaq bid price deficiency notice with an initial compliance period through September 23, 2025, and maintains a $400 million shelf registration and a $75 million sales agreement capacity that could support future financing.