Welcome to our dedicated page for Lisata Therapeutics SEC filings (Ticker: LSTA), 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.
The Lisata Therapeutics, Inc. (LSTA) SEC filings page on Stock Titan provides direct access to the company’s regulatory disclosures as filed with the U.S. Securities and Exchange Commission. Lisata is a clinical-stage pharmaceutical company focused on certepetide, an investigational internalizing RGD cyclic peptide being developed for advanced solid tumors and other serious diseases. Its filings help investors understand how clinical progress, licensing agreements and intellectual property developments are reflected in formal reports.
Recent Form 8-K filings from Lisata have covered topics such as quarterly financial results, preliminary clinical data from the ASCEND trial in metastatic pancreatic ductal adenocarcinoma, corporate presentations used at investor and industry conferences, a new composition of matter patent for certepetide and a worldwide non-exclusive license agreement with Catalent, Inc. for use of certepetide as a SMARTag® antibody-drug conjugate payload. These current reports provide timely detail on material events, including business development milestones and updates to the company’s cash runway expectations.
Through this page, users can track Lisata’s ongoing 8-K disclosures and, as they are filed, review annual reports on Form 10-K, quarterly reports on Form 10-Q, and other materials that describe the company’s clinical programs, risk factors, intellectual property, and financial condition. Stock Titan enhances this information with AI-powered summaries that highlight key points from lengthy documents, helping readers quickly identify items such as new trial data descriptions, changes in development strategy, or licensing and patent developments related to certepetide.
For those following LSTA, this filings archive offers a structured view of Lisata’s regulatory history, from clinical and business updates reported on Form 8-K to broader periodic reports that outline the company’s operations and oncology-focused development plans.
Lisata Therapeutics director Cynthia Louise Flowers reported an equity grant from the company. On January 9, 2026, she was awarded 30,456 shares of common stock in the form of restricted stock units under Lisata’s 2018 Equity Incentive Compensation Plan at a grant price of $0 per share.
These 30,456 restricted stock units are scheduled to vest on January 9, 2027. After this grant, Flowers beneficially owns 95,446 shares of Lisata common stock, which includes the 30,456 unvested restricted stock units.
Lisata Therapeutics director Gregory B. Brown reported receiving 30,456 restricted stock units of common stock on January 9, 2026 under the company’s 2018 Equity Incentive Compensation Plan. These restricted stock units are scheduled to vest on January 9, 2027. Following this grant, he beneficially owns 95,659 shares of Lisata Therapeutics common stock, including 30,456 unvested restricted stock units.
Lisata Therapeutics director granted restricted stock units
Lisata Therapeutics, Inc. director Mohammad Azab reported an award of 30,456 shares of common stock on January 9, 2026. The filing states these are restricted stock units granted under the company’s 2018 Equity Incentive Compensation Plan and that they will vest on January 9, 2027. The units were recorded at a price of $0 per share, reflecting that this was an equity grant rather than an open-market purchase.
After this grant, Azab is reported to beneficially own 104,925 shares of common stock, which the disclosure notes includes 30,456 unvested restricted stock units. The ownership is reported as held directly.
Lisata Therapeutics (LSTA) filed its Q3 2025 10‑Q, reporting a quarterly net loss of $4.249 million as operating expenses declined to $4.414 million from $5.336 million a year ago. Revenue was $0 in the quarter and $70 thousand year‑to‑date.
Liquidity and balance sheet: Cash and cash equivalents were $18.998 million, with total assets of $21.759 million and stockholders’ equity of $17.373 million as of September 30, 2025. The company states it has sufficient cash to meet funding requirements over the next 12 months and expects to seek additional financing by the end of 2026.
Operations and expenses: R&D was $1.959 million and G&A was $2.455 million in Q3. Year‑to‑date, R&D totaled $6.815 million and G&A $8.385 million. The company continued Phase 2 studies of certepetide and delayed certain Phase 3 readiness activities to manage cash.
Capital actions: Lisata raised $600,663 in net proceeds via its ATM during the nine months ended September 30, 2025 and sold $10.7 million of New Jersey NOLs for net proceeds of $871 thousand, recording a $962 thousand deferred income tax benefit.
Lisata Therapeutics (LSTA) furnished an 8-K announcing a press release with financial results for the third quarter ended September 30, 2025, and a corporate presentation. The materials are included as Exhibits 99.1 and 99.2.
These disclosures were provided under Regulation FD and are being furnished, not filed, and therefore are not subject to Section 18 of the Exchange Act nor incorporated by reference except as expressly stated.
Lisata Therapeutics furnished an investor slide presentation under Item 7.01 (Regulation FD). The presentation, dated October 14, 2025, is attached as Exhibit 99.1 and will be used at investor and industry conferences.
The materials are expressly furnished, not filed, under the Exchange Act and are not subject to Section 18 liabilities. They are not incorporated by reference into Securities Act filings unless expressly stated.
Lisata Therapeutics entered into a worldwide non-exclusive license agreement with Catalent, Inc. to allow Catalent to use Lisata's iRGD cyclic peptide, certepetide, as an antibody drug conjugate (ADC) payload on Catalent's SMARTag4 ADC platform. Catalent will assume full responsibility for research, development and commercialization costs, while Lisata is eligible for pre-determined development milestone payments of up to
Lisata Therapeutics (Nasdaq:LSTA) filed an 8-K (Item 7.01 Regulation FD) announcing preliminary cohort B data from its Phase 2 ASCEND trial evaluating certepetide plus standard chemotherapy in metastatic pancreatic ductal adenocarcinoma. The company furnished a press release (Ex. 99.1) and investor slide deck (Ex. 99.2); the 8-K itself contains no numerical efficacy or safety results. Because the information is furnished, it is not deemed “filed” under the Exchange Act and carries no Section 18 liability. The disclosure is potentially material given certepetide’s status as the lead asset targeting a high-mortality cancer, yet the market impact depends on data contained only in the exhibits.