MARKET WIRE NEWS

Hoth Therapeutics Announces Groundbreaking Positive Results: Hoth's HT-VA GDNF Surpasses Semaglutide in Weight Loss, Glucose Control, and Liver Health in Obesity Model

MWN-AI** Summary

Hoth Therapeutics, Inc. (NASDAQ: HOTH) recently revealed compelling preclinical results demonstrating that its innovative therapy, HT-VA GDNF, outperformed semaglutide—active ingredient in the popular obesity treatments Wegovy® and Ozempic®—in several critical health metrics. Conducted with the support of the U.S. Veterans Administration, the study showed that HT-VA GDNF significantly improved weight stabilization, glucose control, liver health, and adipose tissue management, particularly in female mouse models on a high-fat diet.

Key findings included a substantial reduction in weight gain by 10-15% and a pronounced improvement in glucose metabolism, demonstrating normalization of fasting glucose levels. Additionally, GDNF led to a 20-30% decrease in liver weight and effectively prevented adipose tissue accumulation, indicating its potential efficacy in addressing metabolic-associated steatotic liver disease (MASLD), which impacts many adults globally.

These promising preclinical results position GDNF as a vital competitor in the burgeoning $200 billion obesity market, especially given its differentiated mechanism that may mitigate some side effects associated with current GLP-1 agonists, such as gastrointestinal distress and muscle loss. CEO Robb Knie emphasized the breakthrough nature of these findings, envisioning GDNF as a safer and more effective treatment option which could provide life-changing outcomes for patients.

Moving forward, Hoth Therapeutics plans to escalate GDNF's development into Investigational New Drug (IND) enabling studies with clinical trials targeted for 2027. This advancement sits within a wider portfolio of innovative therapies being developed by Hoth, which aim to tackle various unmet medical needs and enhance the quality of life for patients.

MWN-AI** Analysis

Hoth Therapeutics’ recent announcement regarding its HT-VA GDNF treatment presents a pivotal moment in the biotechnology sector, particularly within the burgeoning obesity treatment market, estimated at $200 billion. The preclinical results indicating that GDNF outperforms semaglutide—a well-established GLP-1 agonist—across critical health metrics significantly enhances Hoth's market profile.

Investors should pay close attention to the implications of these findings. Hoth's data showcasing superior weight management, glucose metabolism, and liver health points to a unique therapeutic potential that could differentiate GDNF from current options. The promise of a novel mechanism that mitigates known adverse effects, such as gastrointestinal distress and muscle loss associated with existing treatments, positions GDNF as a potentially safer alternative.

As Hoth advances toward IND-enabling studies and clinical trials expected in 2027, investors ought to consider the following: the potential for strong market adoption once clinical efficacy is established; the impact of regulatory approvals; and the escalating interest from both pharmaceutical partners and investors in innovative obesity treatments.

However, potential investors should also be mindful of the inherent risks. The biotechnology sector is fraught with uncertainties, especially the unpredictable nature of clinical trials and regulatory hurdles that could hinder progress. Given these variables, a prudent approach would be to monitor Hoth’s developments closely while assessing the broader landscape for investment opportunities in companies that focus on innovative weight-loss solutions.

In summary, while Hoth Therapeutics provides an exciting investment proposition with GDNF, informed decisions should incorporate both the potential rewards and risks associated with its advancement in the competitive biopharmaceutical market.

**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.

Source: PR Newswire

PR Newswire

In a head-to-head preclinical comparison, HT-VA co-developed with the United States Veterans Administration GDNF demonstrated superior efficacy compared with semaglutide (the active ingredient in Wegovy®? and Ozempic®?) across key metrics, including weight stabilization, glucose tolerance, liver weight reduction, and adipose tissue control—particularly in female models

NEW YORK, Feb. 10, 2026 /PRNewswire/ -- Hoth Therapeutics, Inc. (NASDAQ: HOTH), a patient-focused biopharmaceutical company developing innovative therapies for unmet medical needs, today announced compelling preclinical data from its VA-backed study on glial cell-derived neurotrophic factor (GDNF) as a novel treatment for obesity and metabolic-associated steatotic liver disease (MASLD). In a head-to-head comparison, GDNF demonstrated superior efficacy over semaglutide (the active ingredient in Wegovy® and Ozempic®) in key metrics, including weight stabilization, glucose tolerance, liver weight reduction, and adipose tissue control—particularly in female models.

This breakthrough positions GDNF as a potential gamechanger in the $200 billion obesity market, offering a differentiated mechanism that could address limitations of current GLP-1 agonists like gastrointestinal side effects and muscle loss. With obesity affecting over 1 billion people globally and MASLD impacting up to 30% of adults, GDNF's multi-faceted benefits could revolutionize treatment paradigms.

Key Study Highlights:

  • Superior Weight Management: In female mice on a high-fat Western diet, GDNF attenuated weight gain by 10-15%, leading to a plateau in the final weeks of treatment—unlike semaglutide, which showed no significant impact. Researchers noted that higher doses or longer durations could amplify GDNF's effects, suggesting even greater potential for sustained weight loss.
  • Enhanced Glucose Metabolism: GDNF fully normalized fasting glucose and improved overall response to glucose challenges, outperforming semaglutide in females. Baseline improvements were also seen in males, indicating broad metabolic benefits.
  • Liver and Adipose Health: GDNF reduced liver weight by 20-30% and prevented adipose tissue accumulation in females, surpassing semaglutide's effects. This underscores GDNF's promise in resolving fatty liver disease, a common complication of obesity.
  • Study Design: Conducted at the Srinivasan Lab with VA support, the 12-week study used CF-1 mice to model human obesity. GDNF was administered subcutaneously with escalating doses (2-12 µg/mouse), compared to semaglutide (12 ng/g/mouse).

"These results are a monumental step forward for Hoth and the fight against obesity," said Robb Knie, CEO of Hoth Therapeutics. "GDNF not only matched but exceeded semaglutide in critical areas, opening doors to a new era of safer, more effective therapies. As we advance this program, we're excited about its potential to deliver life-changing outcomes for patients and significant value for our shareholders."

The study builds on prior research showing GDNF's protective role against diet-induced obesity. Future analyses will include liver pathology, lipid content, and gene/protein expression to further elucidate mechanisms. Hoth plans to accelerate GDNF toward IND-enabling studies, targeting clinical trials in 2027.

Hoth's GDNF program is part of a robust pipeline, including HT-001 (Phase 2 for cancer-related skin toxicities), HT-KIT (Orphan Drug Designation for mast cell cancers), and HT-ALZ (for Alzheimer's).

About Hoth Therapeutics, Inc.

Hoth Therapeutics is a clinical-stage biopharmaceutical company dedicated to developing innovative, impactful, and ground-breaking treatments with a goal to improve patient quality of life. We are a catalyst in early-stage pharmaceutical research and development, elevating drugs from the bench to pre-clinical and clinical testing. Utilizing a patient-centric approach, we collaborate and partner with a team of scientists, clinicians, and key opinion leaders to seek out and investigate therapeutics that hold immense potential to create breakthroughs and diversify treatment options. To learn more, please visit https://ir.hoththerapeutics.com/.

Forward-Looking Statement
This press release includes forward-looking statements based upon Hoth's current expectations, which may constitute forward-looking statements for the purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995 and other federal securities laws, and are subject to substantial risks, uncertainties, and assumptions. These statements concern Hoth's business strategies; the timing of regulatory submissions; the ability to obtain and maintain regulatory approval of existing product candidates and any other product candidates we may develop, and the labeling under any approval we may obtain; the timing and costs of clinical trials, and the timing and costs of other expenses; market acceptance of our products; the ultimate impact of the current coronavirus pandemic, or any other health epidemic, on our business, our clinical trials, our research programs, healthcare systems, or the global economy as a whole; our intellectual property; our reliance on third-party organizations; our competitive position; our industry environment; our anticipated financial and operating results, including anticipated sources of revenues; our assumptions regarding the size of the available market, benefits of our products, product pricing, and timing of product launches; management's expectation with respect to future acquisitions; statements regarding our goals, intentions, plans, and expectations, including the introduction of new products and markets; and our cash needs and financing plans. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. You should not place reliance on these forward-looking statements, which include words such as "could," "believe," "anticipate," "intend," "estimate," "expect," "may," "continue," "predict," "potential," "project" or similar terms, variations of such terms, or the negative of those terms. Although the Company believes that the expectations reflected in the forward-looking statements are reasonable, the Company cannot guarantee such outcomes. Hoth may not realize its expectations, and its beliefs may not prove correct. Actual results may differ materially from those indicated by these forward-looking statements as a result of various important factors, including, without limitation, market conditions and the factors described in the section titled "Risk Factors" in Hoth's most recent Annual Report on Form 10-K and Hoth's other filings made with the U. S. Securities and Exchange Commission. All such statements speak only as of the date made. Consequently, forward-looking statements should be regarded solely as Hoth's current plans, estimates, and beliefs. Investors should not place undue reliance on forward-looking statements. Hoth cannot guarantee future results, events, levels of activity, performance, or achievements. Hoth does not undertake and specifically declines any obligation to update, republish, or revise any forward-looking statements to reflect new information, future events, or circumstances or to reflect the occurrences of unanticipated events, except as may be required by applicable law.

Investor Contact:
LR Advisors LLC
Email: investorrelations@hoththerapeutics.com
www.hoththerapeutics.com
Phone: (678) 570-6791

SOURCE Hoth Therapeutics, Inc.

FAQ**

How might the positive results from Hoth Therapeutics Inc. HOTH's HT-VA GDNF put pressure on current GLP-1 agonist treatments like semaglutide in terms of market competition and patient preference?

Hoth Therapeutics Inc.'s positive HT-VA GDNF results could pressure GLP-1 agonist treatments like semaglutide by presenting a potentially more effective and innovative alternative, thereby influencing market competition and shifting patient preference towards newer therapeutic options.

What steps is Hoth Therapeutics Inc. HOTH planning to take to accelerate the GDNF program towards IND-enabling studies and clinical trials slated for 2027?

Hoth Therapeutics Inc. plans to expedite its GDNF program towards IND-enabling studies and clinical trials in 2027 by advancing preclinical research, seeking partnerships for funding, and focusing on regulatory compliance to enhance development efficiency.

Given that Hoth Therapeutics Inc. HOTH demonstrated superior efficacy for HT-VA GDNF in female models, how does the company plan to address any gender-specific concerns in future clinical trials?

Hoth Therapeutics Inc. plans to incorporate gender-specific analyses and tailored protocols in future clinical trials to effectively address any gender-specific concerns and ensure the efficacy and safety of HT-VA GDNF across diverse populations.

How do Hoth Therapeutics Inc. HOTH's promising findings on GDNF in obesity models position the company in the broader $200 billion obesity market compared to its existing pipeline, including HT-001 and HT-KIT?

Hoth Therapeutics Inc.'s promising findings on GDNF in obesity models may significantly enhance its competitive edge in the $200 billion obesity market by potentially positioning the company for unique therapeutic opportunities that complement its existing pipeline, including HT-001 and HT-KIT.

**MWN-AI FAQ is based on asking OpenAI questions about Hoth Therapeutics Inc. (NASDAQ: HOTH).

Hoth Therapeutics Inc.

NASDAQ: HOTH

HOTH Trading

2.29% G/L:

$1.013 Last:

257,768 Volume:

$1 Open:

mwn-app Ad 300

HOTH Latest News

HOTH Stock Data

$13,480,386
14,440,722
4.13%
11
N/A
Biotechnology & Life Sciences
Healthcare
US
New York

Subscribe to Our Newsletter

Link Market Wire News to Your X Account

Download The Market Wire News App