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Genprex Announces Positive Preliminary Preclinical Data from Study of GPX-002 in Type 2 Diabetic Animal Studies

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Genprex (NASDAQ: GNPX) announced preliminary preclinical in vivo proof-of-concept data for GPX-002, a diabetes gene therapy, from Type 2 diabetic non-human primate (NHP) and mouse studies dated Jan 6, 2026. Key findings: one NHP treated via pancreatic duct infusion achieved normal glucose tolerance at seven months; a second NHP treated by direct pancreatic injection improved glucose tolerance at three months but did not normalize; T2D mice showed statistically significant glucose tolerance improvement at four weeks and restoration of normal glucose levels. Studies used an AAV vector carrying Pdx1 and MafA with an insulin promoter. Ongoing work includes toxicology and IND planning.

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Positive

  • NHP1 achieved normal glucose tolerance at 7 months
  • T2D mice showed normal glucose levels by 4 weeks
  • AAV delivery via pancreatic duct produced multi-month efficacy in NHPs
  • Demonstrated beta cell rejuvenation in both mouse and NHP models

Negative

  • Second NHP improved but did not reach normal glucose tolerance at 3 months
  • NHP studies required a defined period of immunosuppression
  • AAV proteins appear expressed for ~6 months or less, suggesting transient expression
  • Results are preliminary and may not predict human clinical trial outcomes

News Market Reaction – GNPX

+5.00% 3.7x vol
8 alerts
+5.00% News Effect
-19.1% Trough in 33 hr 44 min
+$209K Valuation Impact
$4.38M Market Cap
3.7x Rel. Volume

On the day this news was published, GNPX gained 5.00%, reflecting a notable positive market reaction. Argus tracked a trough of -19.1% from its starting point during tracking. Our momentum scanner triggered 8 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $209K to the company's valuation, bringing the market cap to $4.38M at that time. Trading volume was very high at 3.7x the daily average, suggesting strong buying interest.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

T2D NHPs treated: 2 non-human primates Normal glucose tolerance: 7 months Improved tolerance: 3 months +3 more
6 metrics
T2D NHPs treated 2 non-human primates Preclinical GPX-002 study in Type 2 diabetic NHPs
Normal glucose tolerance 7 months First T2D NHP achieved normal glucose tolerance testing at seven months
Improved tolerance 3 months Second T2D NHP showed significant glucose tolerance improvement at three months
Immunosuppression duration 6 months Initial research suggests no further immunosuppression needed after six months
T2D prevalence range 90–95% of diabetes patients Portion of diabetes patients afflicted by Type 2 diabetes
Post-surgery assessment 4 weeks Glucose tolerance testing in T2D mice four weeks after surgery

Market Reality Check

Price: $0.9750 Vol: Volume 189,768 is in line...
normal vol
$0.9750 Last Close
Volume Volume 189,768 is in line with 20-day average 196,593 (relative volume 0.97x). normal
Technical Price $1.80 trades well below 200-day MA $10.71 and sits 96.73% below the 52-week high, only 5.26% above the 52-week low.

Peers on Argus

Peers show mixed moves: CELZ +2.0%, KPRX +4.48%, RNAZ +3.84% versus CLDI -4.1% a...

Peers show mixed moves: CELZ +2.0%, KPRX +4.48%, RNAZ +3.84% versus CLDI -4.1% and INAB -2.37%, suggesting stock-specific rather than broad biotech momentum for GNPX.

Historical Context

5 past events · Latest: Nov 24 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Nov 24 Phase 1 data Positive -6.7% Publication of Acclaim-1 Phase 1 REQORSA data showing RP2D and early efficacy.
Nov 19 Trial expansion Positive -9.5% Added new clinical site for Acclaim-1 and Acclaim-3 lung cancer trials.
Nov 18 Patent grant Positive -8.7% USPTO patent for REQORSA with PD‑L1 antibodies, protection through 2037.
Nov 4 Patent expansion Positive -11.3% EPO intent to grant patent for REQORSA with PD‑1 antibodies in cancer.
Oct 28 Dilutive offering Negative -20.1% Registered direct offering and warrants for up to $10M gross proceeds.
Pattern Detected

Recent history shows negative reactions to both positive clinical/patent news and dilutive financing, with four divergences on good news and one aligned selloff on an offering.

Recent Company History

Over the last few months, Genprex reported multiple advances around its REQORSA lung cancer program, including patent grants and expansion of Acclaim trial sites, plus publication of Phase 1 data with an RP2D of 0.12 mg/kg. Despite generally constructive clinical and IP updates, shares fell 6–11% on several of these announcements and dropped 20.11% on an October $10.0M registered direct offering. Against this backdrop, today’s positive preclinical diabetes data for GPX-002 adds a separate therapeutic pillar alongside oncology.

Market Pulse Summary

The stock moved +5.0% in the session following this news. A strong positive reaction aligns with the...
Analysis

The stock moved +5.0% in the session following this news. A strong positive reaction aligns with the clearly constructive preclinical data showing GPX-002 normalized glucose tolerance in Type 2 diabetic mice and improved outcomes in non-human primates. However, prior news on REQORSA and financings saw share price weakness despite positive developments, and the stock trades far below its $55 52-week high. Investors would need to weigh early-stage, animal-only data and ongoing capital needs when judging how durable any move might be.

Key Terms

in vivo, proof-of-concept, non-human primate, adeno-associated virus, +4 more
8 terms
in vivo medical
"announced preliminary in vivo preclinical proof-of-concept data for GPX-002"
In vivo describes tests or experiments performed inside a living organism, such as an animal or human, to observe how a drug, device or biological process behaves in a real, functioning body. Investors care because in vivo results reveal safety, effectiveness and possible side effects that lab tests cannot, much like road-testing a prototype car in traffic rather than only on a bench — outcomes can strongly influence regulatory approval, clinical success and a company’s valuation.
proof-of-concept medical
"preliminary in vivo preclinical proof-of-concept data for GPX-002"
A proof-of-concept is a demonstration that shows a new idea or method can work as intended, serving as a small-scale test before full development. For investors, it signals that a concept has been successfully tested in principle, reducing uncertainty about whether it can be practically implemented. This helps determine if further investment or effort is justified to develop the idea further.
non-human primate medical
"in a non-human primate (NHP) model of T2D and in a mouse model"
Non-human primates are animals from the primate family—such as monkeys and apes—excluding humans. Investors should care because these animals are often used in late-stage preclinical testing for drugs and vaccines; their biological similarity to humans makes test results more predictive, so outcomes can materially affect a program’s safety profile, regulatory chances, timeline and cost—like using advanced crash-test dummies that better predict real-world results.
adeno-associated virus medical
"using an adeno-associated virus (AAV) vector containing the Pdx1 and MafA genes"
Adeno-associated virus (AAV) is a naturally occurring, small virus that researchers use as a safe carrier to deliver corrective genes into human cells, much like a specialized delivery van transporting instructions to a malfunctioning machine. It matters to investors because AAV-based therapies drive large development costs, unique manufacturing and regulatory risks, and the potential for high-value, one-time treatments that can significantly affect a biotech company’s future revenue and valuation.
aav vector medical
"using an adeno-associated virus (AAV) vector containing the Pdx1 and MafA genes"
An AAV vector is a harmless, engineered virus used as a microscopic delivery truck to carry therapeutic genes into a patient’s cells. Investors care because AAV-based therapies can produce long-lasting effects from a single treatment, creating potential for big medical and commercial value, but they also bring high development costs, manufacturing challenges and safety and regulatory risks that can sharply affect a company’s prospects.
immunosuppression medical
"Immunosuppression therapy for a defined period of time may prevent immune reaction"
Immunosuppression is the lowering of the immune system’s ability to fight infections and other threats, either from drugs, medical treatments, or underlying disease. For investors it matters because products or conditions that cause immunosuppression change a drug’s safety profile, patient eligibility, regulatory hurdles and market size—think of it like turning down a building’s alarm system, which can reduce false alarms but raises the risk of real break‑ins and affects downstream costs and demand.
investigational new drug (ind) regulatory
"planning formal toxicology studies and subsequent Investigational New Drug (IND) submission"
An investigational new drug (IND) is a drug or biologic that is being tested but has not yet been approved for general use; it is the application and formal status that allows a company to begin human clinical trials under regulator oversight. Investors care because an IND marks the transition from lab work to human testing — like getting a permit to run real-world experiments — which creates important milestones, costs, timelines and regulatory risk that drive a development-stage company's value.
hyperglycemia medical
"the reversal of hyperglycemia in T2D mice and demonstrated normal glucose levels"
Hyperglycemia is a condition where there is too much sugar in the bloodstream because the body cannot move glucose into cells effectively, like a sink with the drain partially blocked so water pools. It matters to investors because persistent high blood sugar drives demand for diabetes treatments, medical devices and hospital care, affects clinical trial outcomes and regulatory decisions, and can signal long-term cost and liability risks for healthcare companies.

AI-generated analysis. Not financial advice.

Preliminary Preclinical Data Demonstrates In Vivo Proof-of-Concept for Novel Diabetes Gene Therapy in Type 2 Diabetic Non-Human Primates

GPX-002 Rejuvenated Exhausted Beta Cells and Normalized Glucose Levels in Type 2 Diabetic Mice

AUSTIN, Texas, Jan. 6, 2026 /PRNewswire/ -- Genprex, Inc. ("Genprex" or the "Company") (NASDAQ: GNPX), a clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes, today announced preliminary in vivo preclinical proof-of-concept data for GPX-002, the Company's diabetes gene therapy drug candidate which may have the potential for long-term control of Type 1 diabetes (T1D) and Type 2 diabetes (T2D), in a non-human primate (NHP) model of T2D and in a mouse model of T2D.

Genprex's research collaborators are conducting preclinical studies of GPX-002 in naturally occurring T2D NHP models. The first NHP was treated with a novel infusion process whereby GPX-002 is administered directly into the pancreatic duct using an adeno-associated virus (AAV) vector containing the Pdx1 and MafA genes and an insulin promoter. The second NHP was treated with GPX-002 by direct injection into the pancreas.

"The progression from mouse model studies into NHP studies demonstrates the progression of preclinical drug development of GPX-002 toward human clinical trials," said Mark Berger, MD, Chief Medical Officer at Genprex. "We have demonstrated proof-of-concept in Type 1 diabetic mouse models, where GPX-002 converted alpha cells into beta-like cells that appropriately produced insulin and normalized blood glucose levels, as well as in Type 2 diabetic mouse models, where beta cells are rejuvenated. Moving into NHP studies in both Type 1 and Type 2 diabetes has enabled us to establish critical proof-of-concept advancements in models that share significant metabolic similarities with humans."

GPX-002 in Type 2 Diabetic Non-Human Primates
Based on the study of the two T2D NHPs, key preliminary data include support for the hypothesis that GPX-002 can rejuvenate exhausted beta cells in T2D. AAV infusion into the pancreatic duct was performed on the first NHP that resulted in improvements in glucose tolerance testing over several months, and at seven months the NHP had normal glucose tolerance testing. This same NHP had severe T2D and abnormally high glucose tolerance testing at baseline just prior to the infusion of the GPX-002 AAV vector. Improvements in glucose tolerance testing, accompanied by decreases in insulin requirements, are consistent with the reprogramming of exhausted beta cells that were rejuvenated by GPX-002 treatment.

Direct pancreas injection in the second NHP resulted in significant improvements in glucose tolerance testing at three months but did not achieve normal glucose tolerance testing results. Pancreatic injection of GPX-002 still shows evidence of efficacy against T2D, however, intraductal infusion appears to be a highly favorable method of delivery to alpha and beta cells.

Immunosuppression therapy for a defined period of time may prevent immune reaction to the AAV. Although T2D studies with AAV constructs in mice do not require immunosuppression, NHPs have an immune response against AAV constructs. AAV proteins appear to be expressed on infected cells for six months or less, as our initial research in the first NHP suggests that after six months no further immunosuppression is required. This new understanding of the need for immunosuppression in NHPs for a defined period of time may lead to better results than the shorter immunosuppression regimens used previously.

"We are highly encouraged by this preliminary preclinical data for GPX-002 in Type 2 diabetes. This work strengthens our existing research, which has already demonstrated improved glucose homeostasis by reprogramming alpha cells in Type 1 diabetes, and now demonstrates potential to unlock treatment opportunities for the remaining 90 to 95 percent of diabetes patients afflicted by Type 2 diabetes utilizing our diabetes technologies," said Ryan Confer, President and Chief Executive Officer at Genprex. "We believe that these results represent significant progress for animal studies of gene therapy for Type 2 diabetes, and we are excited to continue evaluating GPX-002 further in animal studies and move toward human clinical trials."

Researchers are continuing preclinical studies of GPX-002 therapy in NHP models of both T1D and T2D and are planning formal toxicology studies and subsequent Investigational New Drug (IND) submission. Current studies in NHPs are evaluating efficacy after six months of immunosuppression. The results from preclinical testing of GPX-002 may not predict the results that will be obtained in later phase clinical trials of GPX-002.

GPX-002 in Type 2 Diabetic Mice
Genprex's research collaborators have also conducted preclinical studies of GPX-002 in T2D mice, where no immunosuppression was required. In the mouse model, researchers treated T2D mice with a novel infusion process whereby GPX-002 is administered directly into the pancreatic duct using an AAV vector containing the Pdx1 and MafA genes. Researchers showed that in both in vivo and ex vivo studies, T2D mice and diabetic islets treated with GPX-002 demonstrated increased glucose stimulated insulin secretion, thus supporting the novel gene therapy's ability to rejuvenate and replenish exhausted beta cells. In T2D, pancreatic beta cells become unable to produce and secrete enough insulin to manage high blood sugar levels, a condition known as beta cell dysfunction. In this study after GPX-002 treatment, the once exhausted beta cells were rejuvenated, allowing for the proper function of releasing insulin and producing glucose.

At four weeks post-surgery, researchers also conducted glucose tolerance testing which showed statistically significant improvement in T2D mice compared to baseline, the reversal of hyperglycemia in T2D mice and demonstrated normal glucose levels in T2D mice. These results further strengthen GPX-002's capability to rejuvenate and replenish exhausted beta cells in T2D.

About GPX-002
GPX-002 is currently being developed for the treatment of both Type 1 diabetes (T1D) and Type 2 diabetes (T2D). The same general novel approach is used in each of T1D and T2D whereby an adeno-associated virus (AAV) vector containing the Pdx1 and MafA genes is administered directly into the pancreatic duct. In humans, this can be done with a routine endoscopy procedure. In T1D, GPX-002 is designed to work by transforming alpha cells in the pancreas into functional beta-like cells, which can produce insulin but may be distinct enough from beta cells to evade the body's immune system. In vivo, preclinical studies show that GPX-002 restored normal blood glucose levels for an extended period of time in T1D mouse models. In T2D, where autoimmunity is not at play, GPX-002 is believed to rejuvenate and replenish exhausted beta cells.

About Genprex, Inc.
Genprex, Inc. is a clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes. Genprex's technologies are designed to administer disease-fighting genes to provide new therapies for large patient populations with cancer and diabetes who currently have limited treatment options. Genprex works with world-class institutions and collaborators to develop drug candidates to further its pipeline of gene therapies in order to provide novel treatment approaches. Genprex's oncology program utilizes its systemic, non-viral Oncoprex® Delivery System which encapsulates the gene-expressing plasmids using lipid-based nanoparticles in a lipoplex form. The resultant product is administered intravenously, where it is taken up by tumor cells that then express tumor suppressor proteins that were deficient in the tumor. The Company's lead product candidate, Reqorsa® Gene Therapy (quaratusugene ozeplasmid), is being evaluated in two clinical trials as a treatment for NSCLC and SCLC. Each of Genprex's lung cancer clinical programs has received a Fast Track Designation from the FDA for the treatment of that patient population, and Genprex's SCLC program has received an FDA Orphan Drug Designation. Genprex's diabetes gene therapy approach is comprised of a novel infusion process that uses an AAV vector to deliver Pdx1 and MafA genes directly to the pancreas. In models of Type 1 diabetes, GPX-002 transforms alpha cells in the pancreas into functional beta-like cells, which can produce insulin but may be distinct enough from beta cells to evade the body's immune system. In a similar approach for Type 2 diabetes, where autoimmunity is not at play, GPX-002 is believed to rejuvenate and replenish exhausted beta cells.

Interested investors and shareholders are encouraged to sign up for press releases and industry updates by visiting the Company Website, registering for Email Alerts and by following Genprex on Twitter, Facebook and LinkedIn.

Cautionary Language Concerning Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements are made on the basis of the current beliefs, expectations and assumptions of management, are not guarantees of performance and are subject to significant risks and uncertainty. These forward-looking statements should, therefore, be considered in light of various important factors, including those set forth in Genprex's reports that it files from time to time with the Securities and Exchange Commission and which you should review, including those statements under "Item 1A – Risk Factors" in Genprex's Annual Report on Form 10-K for the year ended December 31, 2024.

Because forward-looking statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, statements regarding: Genprex's ability to advance the clinical development, manufacturing and commercialization of its product candidates in accordance with projected timelines and specifications; the timing and success of Genprex's clinical trials, its intended regulatory submissions and any resulting regulatory approvals, including but not limited to, the Company's beliefs about the anticipated effects of GPX-002 and its potential as a therapeutic approach in T1D and T2D; the effect of Genprex's product candidates, alone and in combination with other therapies, on cancer and diabetes; Genprex's future growth and financial status, including Genprex's ability to maintain compliance with the continued listing requirements of The Nasdaq Capital Market and to continue as a going concern and to obtain capital to meet its long-term liquidity needs on acceptable terms, or at all; Genprex's commercial and strategic partnerships, including those with its third party vendors, suppliers and manufacturers and their ability to successfully perform and scale up the manufacture of its product candidates; Genprex's intellectual property and licenses; and Genprex's current expectations, estimates, forecasts and projections about the industry and markets in which it operates.

These forward-looking statements should not be relied upon as predictions of future events and Genprex cannot assure you that the events or circumstances discussed or reflected in these statements will be achieved or will occur. If such forward-looking statements prove to be inaccurate, the inaccuracy may be material. You should not regard these statements as a representation or warranty by Genprex or any other person that Genprex will achieve its objectives and plans in any specified timeframe, or at all. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. Genprex disclaims any obligation to publicly update or release any revisions to these forward-looking statements, whether as a result of new information, future events or otherwise, after the date of this press release or to reflect the occurrence of unanticipated events, except as required by law.

Genprex, Inc.
(877) 774-GNPX (4679)

GNPX Investor Relations
investors@genprex.com 

GNPX Media Contact
Kalyn Dabbs
media@genprex.com 

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/genprex-announces-positive-preliminary-preclinical-data-from-study-of-gpx-002-in-type-2-diabetic-animal-studies-302653395.html

SOURCE Genprex, Inc.

FAQ

What did Genprex (GNPX) report about GPX-002 in Type 2 diabetic non-human primates on January 6, 2026?

Genprex reported preliminary data showing one NHP treated by pancreatic duct infusion reached normal glucose tolerance at 7 months, and a second NHP given direct pancreatic injection showed significant improvement at 3 months.

How did GPX-002 perform in Type 2 diabetic mice in Genprex's preclinical study?

T2D mice treated with GPX-002 showed statistically significant glucose tolerance improvement at 4 weeks and reversal to normal glucose levels.

What delivery methods were tested for GPX-002 in the Genprex preclinical studies?

Researchers tested pancreatic duct infusion (AAV infusion) and direct pancreatic injection, with intraductal infusion appearing more favorable.

Does GPX-002 require immunosuppression in animal studies reported by Genprex?

NHPs required a defined period of immunosuppression due to immune responses to AAV; mice did not require immunosuppression.

What are the next preclinical steps Genprex plans for GPX-002 before human trials?

Genprex is planning formal toxicology studies and an IND submission while continuing NHP efficacy studies.

How durable was AAV expression in the Genprex GPX-002 NHP data?

Initial NHP data suggest AAV proteins are expressed on infected cells for about 6 months or less, reducing the need for ongoing immunosuppression after that period.