*|MC:SUBJECT|*

Dear investor,

DISSEMINATED ON BEHALF OF CONEXEU SCIENCES INC.

Over the last few years, GLP-1 drugs such as Ozempic, Wegovy, and Mounjaro have taken the world by storm and helped millions of people achieve significant weight loss.
 

And the companies behind these drugs have generated substantial revenue — more than $159 billion in less than 10 years.
 

As a result, their stocks have seen significant gains. In one year…
 

…Novo Nordisk — the company behind Ozempic and Wegovy — shot up 82%…
 

…while Eli Lilly — the company behind Mounjaro — soared 98%.
 

And these are companies that had massive market caps before making those gains — $445 billion for Eli Lilly and $358 billion for Novo Nordisk.
 

Yet both of them nearly doubled their market caps — delivering significant returns to their shareholders. 
 

However, there’s a problem — a side effect really — that has created a potential second chance opportunity for investors who missed out on those profits.
 

You’ve probably heard of “Ozempic face” — the term doctors and patients use to describe the hollowed, sagging look that can appear when people lose weight very quickly using these breakthrough new drugs.
 

It’s no fun and patients hate it — so they’re seeking solutions. Many of them are turning to Botox, fillers, and biostimulators… but the results are less than satisfying and wear off quickly.
 

Despite that, Boston Consulting Group estimates that over the next five years, individuals will spend more than $2 billion on these solutions.
 

And that has opened up a massive opportunity for a little-known company I’ve uncovered called Conexeu Sciences (Nasdaq: CNXU). 
 

Conexeu has developed a new regenerative technology designed to support and rebuild facial tissue to help address the effects of Ozempic face.
 

And based on available data and research, it may offer longer-lasting support than Botox, fillers, and biostimulators.


More importantly, it is currently the only company with this technology, which could position it to capture a significant share of this emerging market.


And that could present a noteworthy opportunity for the company and its investors, though all investments carry risk.
 

My name is Robert Kiyosaki, creator of the hugely influential Rich Dad, Poor Dad franchise. 
 

In recent years, I’ve devoted myself to helping ordinary investors identify major wealth trends — before they become obvious to the general public — so they can potentially reap the rewards that come from getting an early jump on those trends.
 

My analysis suggests that treating Ozempic face is rapidly becoming one of those trends… and that Conexeu Sciences (Nasdaq: CNXU) may be well-positioned within this space.
 

You can get all the details in a new Special Report I recently put together. It’s called The Tissue Wall Street Can’t Print, and it reveals all the reasons why I’m so excited about this unique company and the opportunity it represents.
 

To get your free, no-obligation copy of this $199.95-value Report, click here, and you can download it immediately.
 

According to my research and analysis, Conexeu Sciences (Nasdaq: CNXU) may represent a compelling opportunity within this emerging sector focused on helping people address Ozempic face.


And I’m already recommending that subscribers to my Kiyosaki Letter take a close look at the company. I recommend you do the same.
 

Click here now to download your free Special Report.
 

Regards,

Robert Kiyosaki, Editor
The Kiyosaki Letter

Robert Kiyosaki is not securities dealers or brokers, investment advisers or financial advisers, and you should not rely on the information herein as investment advice. Conexeu Sciences Inc. has paid Robert Kiyosaki a fee of $125,000 as consideration for marketing services to be provided over a term of 90 days. [Robert Kiyosaki is a non-arm's-length party who owns zero common shares of Conexeu Sciences Inc.] This newsletter is for informational purposes only. This does not constitute an offer to sell or a solicitation of an offer to buy any securities, nor does it constitute investment, legal, or tax advice. Prospective investors should consult qualified legal, financial, and tax advisors before making any investment decision. The securities issued by the companies we profile should be considered high risk. If you do invest despite these warnings, you may lose your entire investment. Please do your own research before investing, including reading the companies’ SEC and SEDAR+ filings, press releases, and risk disclosures. We also recommend reviewing any applicable prospectus or offering memorandum filed by the company. The information contained in this newsletter was obtained from the company directly, as well as from SEC and SEDAR+ filings, company websites, and other publicly available sources. While we believe such information to be accurate and reliable, we cannot guarantee its accuracy and prospective investors should conduct their own due diligence.

Forward Looking Statements

This newsletter includes certain statements that may be deemed “forward looking statements”. All statements in this newsletter, other than statements of historical facts, that address events or developments that Conexeu Sciences Inc. (the “Company” or “CXU”) expects to occur, are forward looking statements. Forward looking statements are statements that are not historical facts and are generally, but not always, identified by the words “expects”, “plans”, “anticipates”, “believes”, “intends”, “estimates”, “projects”, “potential” and similar expressions, or that events or conditions “will”, “would”, “may”, “could” or “should” occur.

Forward-looking statements include, but are not limited to, statements regarding:  the Company's plans to seek regulatory clearance or approval for its CXU™ product candidates across its target indications, including wound care, dental soft tissue regeneration, veterinary wound care, and medical aesthetics; the Company's anticipated timelines for regulatory submissions, clinical programs, and commercial market entry across its target verticals; the Company's belief that its regulatory strategy will compress timelines and reduce costs relative to alternative regulatory pathways; the Company's expectation that its CXU™ platform is designed to extend across multiple indications from one core formulation; the Company's expectation regarding the manufacturing, storage, and logistical advantages of its product format, including ambient storage capability, point-of-care reconstitution, and global scalability; the Company's beliefs, based on preclinical data, regarding the performance characteristics and clinical potential of its CXU™ product candidates; the Company's expectation regarding its competitive positioning and potential in the medical aesthetics and regenerative medicine markets; and the Company's estimates regarding the size of the total addressable markets across its target verticals.

Forward-looking statements are subject to a variety of known and unknown risks, uncertainties, and other factors that could cause actual events or results to differ from those expressed or implied. There can be no assurance that such statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Certain important factors that could cause actual results, performance or achievements to differ materially from those in the forward-looking statements include, among others: additional capital requirements; inability to obtain sufficient funding; no history of commercial operations; no operating revenues; global financial conditions; regulatory risks, including the risk that applicable regulatory authorities do not grant clearance or approval for the Company's product candidates on anticipated timelines or at all; risks related to research and development activities and the uncertainty of their outcomes; manufacturing and supply chain risks; intellectual property risks; commodity markets; insured and uninsured risks; health, safety and community relations; environmental risks and hazards; currency rate risk; infrastructure; competitive industry environment; government regulation; management and organizational growth; climate change and climate change regulations; risk of litigation; reliance on key personnel; internal controls; conflicts of interest; interest rate risk; credit risk; liquidity risk; risks related to commercialization of the Company's products, including market acceptance, pricing, and reimbursement risks; competition from existing and new market entrants; and uninsurable risks.

Preclinical Status

The CXU™ device candidate is investigational. Statements regarding its mechanism, performance, or potential are based on preclinical findings; clinical significance has not yet been established. The Company has applied to pursue FDA clearance through the 510(k) pathway as a Class II device. There can be no assurance that the Company will obtain clearance on its anticipated timeline, or at all.

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