STOCK TITAN

Jyong Biotech Highlights Multi-Billion Dollar Global BPH Market Opportunity and Reaffirms Strategic Focus on Global Licensing Partnerships

(Neutral)
Tags
partnership

Jyong Biotech (Nasdaq:MENS) is reaffirming its strategic focus on pursuing global licensing partnerships in urology, leveraging its plant-derived drug platform and existing collaborations with multiple international pharmaceutical companies and investment institutions, including a first completed licensing cooperation agreement.

The company highlights the growing benign prostatic hyperplasia (BPH) opportunity, citing 112.5 million patients in 2021 and an estimated global BPH treatment market of about $13 billion in 2025, projected to reach $22–22.6 billion by 2035. Jyong Biotech has conducted four Phase III clinical trials in Taiwan and the US for its investigational BPH drug candidate Botreso® (API-1), incorporating research from over 200 urologists. The company reiterates its commitment to innovation, global patent deployment, and regulatory compliance, while noting that Botreso® remains unapproved for commercial use in any jurisdiction.

Loading...
Loading translation...

Positive

  • First licensing cooperation agreement completed, validating partnering strategy
  • Four Phase III trials completed for Botreso® (API-1) in Taiwan and the US
  • Large BPH market estimated at $13B in 2025, projected up to $22.6B by 2035
  • Research input from 200+ urologists integrated into Botreso® clinical program

Negative

  • Lead BPH candidate Botreso® remains investigational with no approvals in any jurisdiction
  • No commercial revenue disclosed from the first licensing cooperation agreement or partnerships

News Market Reaction – MENS

+2.65%
10 alerts
+2.65% Session close to close
-9.6% Trough in 4 hr 32 min
$201.17M Market Cap
0.7x Rel. Volume

In the Jul 23 session, MENS gained 2.65%, reflecting a moderate positive market reaction. Argus tracked a trough of -9.6% from its starting point during tracking. Our momentum scanner triggered 10 alerts that day, indicating notable trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

Risk context listed short positioning as low. That platform signal adds limited crowding context to ...
Analysis

Risk context listed short positioning as low. That platform signal adds limited crowding context to Jyong Biotech's licensing emphasis, while the 20-F's disclosed API-1 trial failure and possible additional studies remain material risks to monitor.

Key Figures

Global BPH patients: 112.5 million Patient population increase: over 122% Projected BPH patients: 150 million to 156 million +5 more
8 metrics
Global BPH patients 112.5 million 2021
Patient population increase over 122% 2021 versus 1990
Projected BPH patients 150 million to 156 million 2035
BPH treatment market approximately $13 billion 2025
Projected BPH treatment market $22 billion to $22.6 billion 2035
Market growth nearly 70% 2025 to 2035
Five-year discontinuation rate 60% to 90% Existing BPH treatments
Phase III trials four trials Botreso in Taiwan and the US

Historical Context

5 past events · Latest: Jul 02 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jul 02 BIO portfolio showcase Positive +8.3% BIO 2026 portfolio showcase and global licensing emphasis
May 29 FDA pathway update Positive -2.2% CEO outlined FDA pathway, clinical plans, and global commercialization strategy
May 15 Annual report filing Neutral -3.4% Company filed its Form 20-F annual report for fiscal 2025
Apr 28 Market access update Positive +0.9% Company updated market access strategy for Botreso and PCP
Mar 27 Clinical benefits update Positive -4.0% Company updated clinical and intellectual-property highlights for MCS-2

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

The stock's recent record was mixed, with three of five prior updates diverging from this announcement's positive strategic tone.

Key Terms

benign prostatic hyperplasia, 5-alpha reductase inhibitors, orthostatic hypotension, phase iii clinical trials, +1 more
5 terms
benign prostatic hyperplasia medical
"made Benign Prostatic Hyperplasia (BPH) one of the most common urinary system diseases"
Benign prostatic hyperplasia is a noncancerous enlargement of the prostate gland that can squeeze the urethra and cause urinary symptoms like weak stream, urgency, and incomplete emptying; think of it as a garden hose being pinched so water flow slows. It matters to investors because it creates steady demand for medications, medical devices and procedures, regulatory approvals, and insurance coverage decisions—factors that can drive revenue and growth in healthcare companies serving an aging population.
5-alpha reductase inhibitors medical
"medications such as alpha-blockers and 5-alpha reductase inhibitors (5-ARIs)"
Drugs that block the enzyme 5-alpha reductase, which converts the male hormone testosterone into a more active form called dihydrotestosterone (DHT). By lowering DHT levels, these medicines can shrink prostate tissue and slow certain types of hair loss, so they matter to investors because trial results, approvals, or sales affect the valuation and revenue potential of companies developing or marketing them. Think of the enzyme as a tap that the drug partly shuts off to reduce the downstream effect.
orthostatic hypotension medical
"adverse effects like dizziness, orthostatic hypotension, ejaculatory dysfunction"
A sudden drop in blood pressure that happens when a person stands up from sitting or lying down, causing dizziness, lightheadedness, or fainting. For investors, it matters because treatments, drug side effects, or medical-device performance tied to this condition can affect regulatory approval, product labeling, and patient adoption—similar to a car that stalls on a hill, creating safety concerns that influence market value and sales prospects.
phase iii clinical trials technical
"advance an oral botanical new drug to U.S. FDA Phase III clinical trials"
Phase III clinical trials are large, late-stage studies that test whether a drug or medical treatment is safe and effective when used in the general patient population, often comparing it to existing treatments or a placebo. Investors watch Phase III results closely because they are the final major test before regulators decide on approval—like a final road test that determines whether a product can be sold widely and generate meaningful revenue.
investigational new drug candidate regulatory
"Botreso® remains an investigational new drug candidate"
A investigational new drug candidate is a chemical or biological compound that a company is testing in regulated preclinical or clinical studies but has not yet received marketing approval from health authorities. It matters to investors because its successful testing and regulatory milestones are central drivers of future revenues and company valuation, while failed trials or safety issues can substantially reduce expected value—think of it like a prototype product undergoing safety and performance road tests.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

New Taipei City, Taiwan, July 23, 2026 (GLOBE NEWSWIRE) -- Jyong Biotech Ltd. (Nasdaq: MENS) (the "Company" or "Jyong Biotech"), a science-driven biotechnology company dedicated to the development and commercialization of innovative plant-derived therapeutics, today reaffirmed its strategic focus on pursuing global licensing partnerships to address the growing medical needs in the urology sector. Building upon the momentum of its recent participation at the BIO 2026 International Convention, the Company continues to actively engage in discussions with international pharmaceutical companies and industry partners across multiple regions, aiming to continuously expand its global cooperation network.

As the first Taiwanese company to advance an oral botanical new drug to U.S. FDA Phase III clinical trials, Jyong Biotech leverages its differentiated botanical drug platform to advance presence in the global botanical drug market.

Having already established collaborative relationships with multiple international pharmaceutical companies and investment institutions, and successfully completed its first licensing cooperation agreement, the Company remains dedicated to its core strategy of innovation and global patent deployment.

A key driver of Jyong Biotech's ongoing partnership discussions is the accelerating trend of global population aging, which has made Benign Prostatic Hyperplasia (BPH) one of the most common urinary system diseases among men globally. As the prostate enlarges with age, it causes obstructive symptoms, such as a weak urinary stream, incomplete emptying, terminal dribbling, intermittency, and straining, as well as irritative symptoms like urinary frequency, urgency, and nocturia, all of which severely impact quality of life. Long-term sufferers are also prone to complications including bacterial cystitis, bladder stones, urinary retention, and renal function impairment.

According to the Global Burden of Disease (GBD 2021) and BMC Urology research, the global BPH patient population reached 112.5 million in 2021, representing an increase of over 122% from 50.7 million in 1990, and is projected to grow to between 150 million and 156 million by 2035. Correspondingly, the global BPH treatment market size is estimated at approximately $13 billion in 2025 and is expected to grow to $22 billion to $22.6 billion by 2035, growing nearly 70% over a decade. Despite this market growth, a significant unmet medical need remains due to the severe side effects and high discontinuation rates of existing treatments. Current BPH treatments primarily rely on medications such as alpha-blockers and 5-alpha reductase inhibitors (5-ARIs). However, these drugs are associated with a five-year discontinuation rate of 60% to 90% due to adverse effects like dizziness, orthostatic hypotension, ejaculatory dysfunction, and sexual dysfunction.

Jyong Biotech is focused on addressing this unmet need. Having actively engaged in discussions with international pharmaceutical companies and industry partners, the Company remains dedicated its core strategy of innovation and global patent deployment. Additionally, the Company has conducted four Phase III clinical trials for its BPH new drug candidate, Botreso® (API-1) in Taiwan and the US, incorporating research from over 200 urologists. Ms. Fu-Feng Kuo, Chairwoman of Jyong Biotech, who has personally led the research team for over twenty years, stated, "The aging of the global population is an irreversible trend, and the number of BPH patients will continue to increase rapidly. We remain steadfast in our commitment to scientific evidence and innovative research, striving to provide patients with safer treatment options that are suitable for long-term use, while continuously exploring strategic avenues to introduce the independently developed botanical new drugs to the global market."

As of the date of this press release, Botreso® remains an investigational new drug candidate and has not been approved for commercial use in any jurisdiction. Jyong Biotech will comply with applicable regulatory disclosure obligations and provide timely, accurate, and complete updates on material developments.

About Jyong Biotech Ltd.
Headquartered in Taiwan, Jyong Biotech Ltd. is a science-driven biotechnology company committed to developing and commercializing innovative and differentiated new drugs (plant-derived), mainly specializing in the treatment of urinary system diseases, with an initial focus on the markets of the U.S., the EU and Asia. Since its inception in 2002, the Company has built integrated capabilities that encompass all key functionalities of drug development, including early-stage drug discovery and development, pharmacology, toxicology, clinical trials, regulatory affairs, manufacturing, and commercialization. Leveraging strong research and development capabilities and a proprietary platform, the Company has been developing a series of botanical drug candidates, including its primary botanical drug candidate, BOTRESO®, another clinical-stage botanical drug candidate, and other preclinical-stage botanical drug candidates. The Company endeavors to develop and supply first-class innovative drugs to meet customers' health needs and seeks to be a valuable business organization that is held in high esteem by the public.
For more information, please visit: https://www.jyongbio.com/, https://jyongir.com/.

Forward-Looking Statement
This press release contains forward-looking statements. Forward-looking statements include statements concerning plans, objectives, goals, strategies, future events or performance, and underlying assumptions and other statements that are other than statements of historical facts. When the Company uses words such as “may, “will, “intend,” “should,” “believe,” “expect,” “anticipate,” “project,” “estimate” or similar expressions that do not relate solely to historical matters, it is making forward-looking statements. Forward-looking statements are not guarantees of future performance and involve risks and uncertainties that may cause the actual results to differ materially from the Company's expectations discussed in the forward-looking statements. These statements are subject to uncertainties and risks including, but not limited to, the uncertainties related to market conditions and other factors discussed in the “Risk Factors” section of the registration statement, prospectuses, annual and interim reports, and other filings with the SEC. For these reasons, among others, investors are cautioned not to place undue reliance upon any forward-looking statements in this press release. Additional factors are discussed in the Company's filings with the SEC, which are available for review at www.sec.gov. The Company undertakes no obligation to publicly revise these forward-looking statements to reflect events or circumstances that arise after the date hereof.

For more information, please contact:
Jyong Biotech Ltd.
ir@jyongbio.com
Email: vivi.z@jyongbio.com
Mobile: +1 (646) 307-3803

Investor Relations
WFS Investor Relations Inc.
Email: services@wfsir.com
Phone: +1 628 283 9214


FAQ

What strategic focus did Jyong Biotech (MENS) reaffirm on July 23, 2026?

Jyong Biotech reaffirmed a strategic focus on global licensing partnerships in urology. According to Jyong Biotech, the company is engaging international pharmaceutical and industry partners to expand its cooperation network and bring its botanical drug candidates to major markets in the US, EU and Asia.

How large is the global BPH market opportunity highlighted by Jyong Biotech (MENS)?

Jyong Biotech highlighted an estimated global BPH treatment market of about $13 billion in 2025. According to Jyong Biotech, this market is projected to grow to roughly $22–22.6 billion by 2035, nearly a 70% increase over a decade, driven by population aging.

What clinical progress has Jyong Biotech reported for Botreso (API-1) for BPH?

Jyong Biotech has conducted four Phase III clinical trials for Botreso® (API-1) in Taiwan and the US. According to Jyong Biotech, these trials incorporated research contributions from more than 200 urologists, supporting its efforts to develop a plant-derived BPH therapy for long-term use.

Is Jyong Biotech’s BPH drug candidate Botreso approved for commercial use?

Botreso® remains an investigational new drug candidate and is not approved anywhere. According to Jyong Biotech, as of July 23, 2026, the product has no commercial authorization in any jurisdiction, and the company will provide timely regulatory and clinical updates as required.

What unmet medical need in BPH treatment is Jyong Biotech (MENS) targeting?

Jyong Biotech aims to address unmet needs linked to side effects and discontinuation of current BPH drugs. According to Jyong Biotech, existing alpha-blockers and 5-ARIs show five-year discontinuation rates of 60–90% due to dizziness, orthostatic hypotension, and sexual or ejaculatory dysfunction.

How does Jyong Biotech’s platform support its global licensing strategy for BPH therapies?

Jyong Biotech leverages an integrated botanical drug platform spanning discovery through commercialization. According to Jyong Biotech, it has existing collaborations with multiple international pharmaceutical companies and investors, completed its first licensing cooperation agreement, and focuses on global patent deployment to support future licensing deals.

What geographic markets is Jyong Biotech (MENS) initially targeting for its botanical drugs?

Jyong Biotech is initially focusing on the US, EU and Asian markets for its plant-derived drugs. According to Jyong Biotech, the company is building international partnerships and regulatory capabilities to introduce independently developed botanical new drugs across these key urology markets.