Genprex, Inc. 8-K Filing

Ticker: GNPX · Form: 8-K · Filed: Nov 18, 2025 · CIK: 1595248

Genprex, Inc. 8-K Filing Summary
FieldDetail
CompanyGenprex, Inc. (GNPX)
Form Type8-K
Filed DateNov 18, 2025
Pages4
Reading Time5 min
Key Dollar Amounts$0.001
Sentimentneutral

Sentiment: neutral

FAQ

What type of filing is this?

This is a 8-K filing submitted by Genprex, Inc. (ticker: GNPX) to the SEC on Nov 18, 2025.

What are the key financial figures in this filing?

Key dollar amounts include: $0.001 (h registered Common Stock , par value $0.001 per share GNPX The Nasdaq Capital Ma).

How long is this filing?

Genprex, Inc.'s 8-K filing is 4 pages with approximately 1,316 words. Estimated reading time is 5 minutes.

Where can I view the full 8-K filing?

The complete filing is available on SEC EDGAR. You can also read the AI-decoded analysis with risk assessment and key highlights on ReadTheFiling.

Filing Stats: 1,316 words · 5 min read · ~4 pages · Grade level 14.8 · Accepted 2025-11-18 07:10:17

Key Financial Figures

  • $0.001 — h registered Common Stock , par value $0.001 per share GNPX The Nasdaq Capital Ma

Filing Documents

01 Other Events

Item 8.01 Other Events. On November 18, 2025, Genprex, Inc. ("Genprex" or the "Company") issued a press release in which it announced that the United States Patent and Trademark Office has granted Genprex a patent that covers the use of the Company's lead drug candidate, Reqorsa Gene Therapy (quaratusugene ozeplasmid), in combination with PD-L1 antibodies, such as Tecentriq, through 2037. The press release noted that in the Acclaim-3 clinical trial, the Company is combining REQORSA with Tecentriq, a PD-L1 antibody, and this patent secures exclusivity for this drug combination for the treatment of cancer, preventing would-be competitors from making, using or selling this drug combination. PD-L1 antibodies are a type of targeted immunotherapy that block the activity of PD-L1 immune checkpoint proteins present on the surface of cells. Genprex has been granted patents for the use of REQORSA in combination with PD-L1 antibodies in the U.S. and Korea. Genprex is pursuing additional patent applications in Europe, Canada, Brazil, China and Israel. Should these applications grant, they would also be applicable to Genprex's Acclaim-3 clinical trial. Acclaim-3 is a Phase 1/2 clinical trial evaluating the combination of REQORSA and Genentech's Tecentriq (atezolizumab) as maintenance therapy in patients with extensive stage small cell lung cancer ("ES-SCLC") who are candidates for maintenance therapy after receiving Tecentriq and chemotherapy as standard of care initial treatment. In this study, patients will be treated with REQORSA and Tecentriq until disease progression or unacceptable toxicity is experienced. The Phase 2 expansion study follows the successful completion of the Phase 1 dose escalation portion of the study, which showed REQORSA was generally well tolerated. There were no dose limiting toxicities, and in Acclaim-3, the Phase 2 patients are receiving the same dose of REQORSA as patients in the Phase 2 portion of Acclaim-1. The Phase 2 expansion portion is exp

01 Financial Statements and Exhibits

Item 9.01 Financial Statements and Exhibits. (d) Exhibits. Exhibit Number Description 104 Cover Page Interactive Data File (embedded within the Inline XBRL document).

SIGNATURES

SIGNATURES Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized. GENPREX, INC. Date: November 18, 2025 By: /s/ Ryan Confer Ryan Confer Chief Executive Officer and Chief Financial Officer (Principal Executive Officer and Principal Financial and Accounting Officer)

View Full Filing

View this 8-K filing on SEC EDGAR

View on ReadTheFiling | About | Contact | Privacy | Terms

Data from SEC EDGAR. Not affiliated with the SEC. Not investment advice. © 2026 OpenDataHQ.