Welcome to our dedicated page for Crinetics Pharmaceuticals SEC filings (Ticker: CRNX), 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.
Crinetics Pharmaceuticals, Inc. filings document a commercial-stage pharmaceutical company focused on endocrine diseases and endocrine-related tumors. Its 8-K reports include financial results and business updates tied to PALSONIFY product revenue, clinical development activity, regulatory matters, and corporate presentations. The filings also identify the company’s common stock, traded under CRNX on the Nasdaq Global Select Market.
Crinetics’ regulatory record also includes proxy materials covering governance and executive compensation, as well as current reports on officer responsibilities, executive departures, consulting arrangements, and changes in the company’s independent registered public accounting firm. These disclosures place PALSONIFY commercialization and endocrine pipeline development within formal reporting categories for operations, governance, controls, and capital-market status.
Crinetics Pharmaceuticals (CRNX) filed a Form 144 disclosing a proposed sale of 30,000 shares of Common stock through Morgan Stanley Smith Barney with an aggregate market value of $882,000, to be sold on 08/22/2025 on NASDAQ. The shares were reported acquired that same day on 08/22/2025 by exercise of stock options from the issuer, with cash payment reported for the option exercise.
The filing also lists prior 10b5-1 sales by Dana Pizzuti of 6,492 shares on 08/20/2025 generating gross proceeds of $189,426.82. The notice includes the standard representation that the seller is not aware of undisclosed material adverse information.
Insider sale by Dana Pizzuti, Chief Medical and Development Officer of Crinetics Pharmaceuticals (CRNX). On 08/20/2025 Ms. Pizzuti sold 6,492 shares of Crinetics common stock in open-market transactions at a volume-weighted average price of $29.18 per share, with the intraday price range $28.94 to $29.47. The sale was effected automatically under a Rule 10b5-1 trading plan adopted May 21, 2025.
Following the reported transactions she beneficially owned 66,270 shares, which includes 529 shares acquired under the companys Employee Stock Purchase Plan. The Form 4 was signed by an attorney-in-fact on 08/21/2025.
Crinetics Pharmaceuticals (CRNX) filed a Form 144 reporting a proposed sale of 6,492 common shares valued at $191,059.56 with an approximate sale date of 08/20/2025 on NASDAQ. The filing lists total shares outstanding of 94,175,994. The securities were acquired as 4,360 restricted stock units on 03/15/2025 and 2,132 shares through an employee stock purchase plan on 05/20/2023. The filer reports no securities sold in the past three months. Several standard filer contact and issuer identification fields in the provided content are blank or not provided.
Wellington Management reporting persons disclose beneficial ownership of 5,807,308 shares of Crinetics Pharmaceuticals common stock, representing 6.2% of the class. The stake is reported across multiple Wellington entities (holding companies and investment advisers) and is held of record by clients of the Wellington investment advisers.
The filing shows no sole voting or dispositive power reported by the filers and reports shared voting power and shared dispositive power across the Wellington entities. The filers certify the securities are held in the ordinary course of business and not for the purpose of changing control.
Crinetics Pharmaceuticals (Nasdaq:CRNX) furnished an 8-K covering its June 26 2025 R&D Day. Management unveiled new pre-clinical data on three assets—TSHR antagonist CRN12755 for Graves’ disease, SST3 agonist CRN10329 for ADPKD and drug-conjugate CRN09682 for SST2-positive tumors—and outlined the Phase 1/2 BRAVESST2 design enrolling up to 150 patients. Highlights include reductions in thyroid hormone, hyaluronic acid, IL-6 and cystic indices, plus dose-dependent anti-tumor activity. No financial results or guidance were provided; information is “furnished,” not “filed,” and forward-looking statements stress clinical, regulatory and financing risks.