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MIAMI, FL / ACCESS Newswire / June 18, 2025 / MIRA Pharmaceuticals, Inc. (Nasdaq:MIRA) (“MIRA” or the “Company”), a clinical-stage pharmaceutical company developing novel therapeutics for neurologic, neuropsychiatric, and metabolic disorders, today announced that the first manuscript describing its lead drug candidate Ketamir-2, currently being evaluated in an ongoing Phase 1 clinical trial for neuropathic pain, has been accepted for publication in the peer-reviewed journal Frontiers in Pharmacology.

The article, titled “KETAMIR-2, A NEW MOLECULAR ENTITY AND NOVEL KETAMINE ANALOG,” authored by Itzchak Angel, Ph.D., MIRA’s Chief Scientific Advisor, highlights Ketamir-2’s pharmacological differentiation from ketamine and its potential as a next-generation CNS therapeutic.

Peer Review Validates Differentiated Pharmacology and Safety

Acceptance into Frontiers in Pharmacology provides external scientific validation by independent experts, underscoring the rigor and credibility of MIRA’s research. The publication confirms that Ketamir-2 was specifically engineered to overcome limitations associated with ketamine-such as poor oral bioavailability, dissociative side effects, and non-specific receptor binding.

Key Highlights from the Publication:

• Highly Selective, Cleaner Mechanism: Ketamir-2 is a low-affinity NMDA receptor antagonist that selectively targets the NMDA PCP site. Unlike ketamine, Ketamir-2 showed no significant interaction with over 40 other receptors, transporters, or ion channel targets-including dopamine, opioid, serotonin, and monoaminergic systems-highlighting its clean pharmacological profile and reduced off-target effects.

• No Hyperlocomotion, Even at High Doses: In contrast to ketamine, Ketamir-2 did not induce hyperlocomotion in preclinical models-a behavior associated with agitation and schizophrenia-like symptoms-suggesting a favorable neurobehavioral safety profile.

• Demonstrated Antidepressant and Anxiolytic Activity: In validated behavioral models (Open Field Test, Elevated Plus Maze, Forced Swim Test), Ketamir-2 demonstrated clear anxiolytic and antidepressant-like effects. Ketamine, used as a control, either showed no benefit or limited effect in most tests.

• Oral Delivery with Efficient Brain Penetration: All studies were conducted via the oral route. Ketamir-2 was shown to cross the blood-brain barrier and is not a substrate for P-glycoprotein, which often limits oral drug delivery to the brain. This may explain Ketamir-2’s ability to maintain CNS activity despite its lower NMDA receptor affinity.

“We are honored to see our foundational research on Ketamir-2 published in a high-impact scientific journal,” said Erez Aminov, CEO of MIRA. “This milestone adds meaningful scientific credibility and supports our confidence in Ketamir-2’s differentiated mechanism, favorable safety profile, and broad clinical potential.”

“This peer-reviewed publication provides clear validation of the differentiated pharmacological profile of Ketamir-2,” added Dr. Itzchak Angel, Chief Scientific Advisor. “Its clean pharmacological profile and safety make it a compelling next-generation alternative to ketamine.”

Clinical and Corporate Updates

MIRA also announced that its Phase 1 trial of Ketamir-2 is progressing as planned, with no safety concerns reported to date and dose escalation advancing. The Company expects to initiate a Phase 2a clinical trial in neuropathic pain by year-end 2025, pending regulatory clearance.

In addition, the Company is preparing new scientific data submissions and presentations to further support Ketamir-2’s clinical development and potential across CNS-related conditions.

MIRA also reaffirmed that the acquisition of SKNY Pharmaceuticals, which includes a first-in-class oral CB1/CB2 inverse agonist for obesity and smoking cessation (SKNY-1), is progressing on track. The Company has submitted the required regulatory filings for the merger to the U.S. Securities and Exchange Commission (SEC).

The publication will be available upon release at: www.frontiersin.org/journals/pharmacology

Cautionary Note Regarding Forward-Looking Statements

This press release and the statements of MIRA’s management related thereto contain “forward-looking statements,” which are statements other than historical facts made pursuant to the safe harbor provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements may be identified by words such as “aims,” “anticipates,” “believes,” “could,” “estimates,” “expects,” “forecasts,” “goal,” “intends,” “may,” “plans,” “possible,” “potential,” “seeks,” “will,” and variations of these words or similar expressions that are intended to identify forward-looking statements. Any statements in this press release that are not historical facts may be deemed forward-looking. Any forward-looking statements in this press release are based on MIRA’s current expectations, estimates, and projections only as of the date of this release and are subject to a number of risks and uncertainties (many of which are beyond MIRA’s control) that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements, including related to MIRA’s potential merger with SKNY Pharmaceuticals, Inc. These and other risks concerning MIRA’s programs and operations are described in additional detail in the Annual Report on Form 10-K for the year ended December 31, 2024, and other SEC filings, which are on file with the SEC at www.sec.gov and MIRA’s website at https://www.mirapharmaceuticals.com/investors/sec-filings. MIRA explicitly disclaims any obligation to update any forward-looking statements except to the extent required by law.

Contact Information

Helga Moya
info@mirapharma.com
(786) 432-9792

SOURCE: MIRA Pharmaceuticals

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ROSH HA‘AYIN, IL / ACCESS Newswire / June 18, 2025 / Brenmiller Energy Ltd. (“Brenmiller”, “Brenmiller Energy” or the “Company”) (NASDAQ:BNRG), a leading global provider of Thermal Energy Storage (“TES”) solutions for industrial and utility customers, today issued a letter from its Chief Executive Officer, Avi Brenmiller.

To Our Shareholders,

As previously announced, today at the close of trading on the Nasdaq Capital Market, Brenmiller Energy will implement a reverse share split-a strategic and proactive decision made to protect and preserve shareholder value as we approach a critical period of execution on our business objectives.

This decision followed extensive internal consideration about the timing and impact of a reverse share split. Ultimately, we determined that the best course of action was to be decisive today, which will allow us to remain focused on what matters most in the days ahead: delivering on our milestones.

The value that Brenmiller Energy has built is evident:

• More than a decade of TES innovation and $118 million in investments have led to deployments across Europe, the U.S., and the Middle East

• Commissioning and building over 100 MWh of projects

• A $500 million pipeline of commercial opportunities

• 4GWh of manufacturing capacity

Let us be clear: a reverse split changes the number of shares outstanding, but it does not impact your ownership.

All shareholders-including insiders-are impacted equally by this reverse split. That’s not incidental. It’s intentional. We are all in this together. Our Company’s founders and management, including myself, continue to have significant holdings in Brenmiller Energy. Investors can be assured that all of our interests are aligned.

As we are aiming to move towards key implementation milestones for commercial deployment in the near-term, with funding commitments for projects within our existing portfolio, and strategic collaborations-we believe that these future achievements will translate into tangible value for shareholders.

We’re not waiting for the market to understand what we’ve built. We are aiming to make it impossible to ignore.

As we’ve shared throughout 2025, we believe that Brenmiller Energy has entered a new phase-one defined by acceleration. Our recent progress with TES projects including Tempo Beverages in Israel and SolWinHy in Spain makes that clear: we believe we are on the verge of a breakout moment with a robust global commercial pipeline and technology that’s already proven in the field.

The result? Real operating momentum that we believe will spark interest in our technology-and a reappraisal of the value it truly deserves.

We thank you for standing with us, and we invite you to stay close. We believe that the weeks ahead won’t just validate our vision-they’ll define it.

Sincerely,

Avi Brenmiller
CEO, Brenmiller Energy Ltd.

About Brenmiller Energy Ltd.

Brenmiller Energy helps energy-intensive industries and power producers end their reliance on fossil fuel boilers. Brenmiller’s patented bGen™ ZERO thermal battery is a modular and scalable energy storage system that turns renewable electricity into zero-emission heat. It charges using low-cost renewable electricity and discharges a continuous supply of heat on demand and according to its customers’ needs. The most experienced thermal battery developer on the market, Brenmiller operates the world’s only gigafactory for thermal battery production and is trusted by leading multinational energy companies. For more information visit the Company’s website at https://bren-energy.com/ and follow the company on X and LinkedIn.

Forward-Looking Statements:

This press release contains “forward-looking statements” within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995 and other federal securities laws. Statements that are not statements of historical fact may be deemed to be forward-looking statements. For example, the Company is using forward-looking statements when it discusses: expected near-term milestones; the timing for implementing a reverse share split; its protecting and preserving shareholder value as the Company approaches a critical period of execution its business objectives;; the Company’s future commercial deployment milestones, funding commitments for projects within its existing portfolio, and strategic collaborations and that such future achievements will translate into tangible value for shareholders; future interest in the Company’s technology and a reappraisal of its value; and the Company’s $500 million pipeline of commercial opportunities. Without limiting the generality of the foregoing, words such as “plan,” “project,” “potential,” “seek,” “may,” “will,” “expect,” “believe,” “anticipate,” “intend,” “could,” “estimate” or “continue” are intended to identify forward-looking statements. Readers are cautioned that certain important factors may affect the Company’s actual results and could cause such results to differ materially from any forward-looking statements that may be made in this press release. Factors that may affect the Company’s results include, but are not limited to: the Company’s planned level of revenues and capital expenditures; risks associated with the adequacy of existing cash resources; the demand for and market acceptance of our products; impact of competitive products and prices; product development, commercialization or technological difficulties; the success or failure of negotiations; trade, legal, social and economic risks; and political, economic and military instability in the Middle East, specifically in Israel. The forward-looking statements contained or implied in this press release are subject to other risks and uncertainties, many of which are beyond the control of the Company, including those set forth in the Risk Factors section of the Company’s Annual Report on Form 20-F for the year ended December 31, 2024 filed with the U.S. Securities and Exchange Commission (“SEC”) on March 4, 2025, which is available on the SEC’s website, www.sec.gov. The Company undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.

Contact: investors@bren-energy.com

SOURCE: Brenmiller Energy

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NEWPORT BEACH, CALIFORNIA / ACCESS Newswire / June 18, 2025 / Amaze Holdings Inc. (NYSE American:AMZE) (“Amaze” or the “Company”), a global leader in creator-powered commerce, today announced, that new directors Pete Deutschman, Amrapali (Ami) Gan, and Sandie Hawkins were elected to its Board of Directors at the annual meeting of stockholders, effective June 12, 2025. The new appointees collectively will offer added corporate governance support and a diversified range of strategic insights to Amaze’s executive leadership team.

“With the expanded market opportunity and new strategic direction of our combined Company, we’ve accordingly bolstered our board of directors with an impressive group of industry veterans with deep ties to the creator economy,” Amaze Vice-Chairman Michael Pruitt said. “Our new board members offer a wide range of entrepreneurial experience and a deep knowledge across a variety of ecommerce, marketing, and creator-specific industries. On behalf of the rest of our board, I would like to welcome our newest members, and we look forward to benefiting from their contributions as we execute our mission to uplift and transform the creator economy.”

Pete Deutschman, Director

Pete Deutschman is Chief Buddy and Founder of The Buddy Group, an end-to-end creative marketing firm that helps brands engage with audiences and drive growth. At The Buddy Group, Deutschman has managed engagements with McDonald’s, American Express, Yamaha, and others. Deutschmanis also an advisor to a handful of technology start-ups, including Exfluential, Vessl, SailPlan, and DotLot, and is a board member for Project Hope Alliance.

Ami Gan, Director

Ami Gan is the Founder of HOXTON, a strategic advisory firm that blends strategy with creativity. Prior to founding HOXTON, Gan was the CEO of OnlyFans and led the company’s expansion into new creator segments globally. Gan also previously held various positions with global rapid-growth companies within disruptor industries including Cannabis Cafe, Red Bull Media House, and Quest Nutrition.

Sandie Hawkins, Director

Sandie Hawkins is the President at Teikametrics, an AI marketplace optimization platform, and has over 20 years of expertise in multi-channel marketing, business development, and digital innovation. Prior to this role, Hawkins served as General Manager of TikTok’s United States e-commerce business, where she launched TikTok shop and spearheaded the platform’s e-commerce strategy. She has also held various leadership roles at Adobe, Varick, and Rocket Fuel, where she developed high-performing teams, launched innovative digital solutions, and cultivated strategic partnerships.

Capitalization Update

The Company announced that the number of shares of common stock outstanding is 5,277,810 as of June 16, 2025, after taking into account the recent conversion of the Company’s Series D convertible preferred stock into common stock and the 1-for-23 reverse stock split effected on June 12, 2025.

For investor information, please contact IR@amaze.co

For press inquiries, please contact PR@amaze.co

About Amaze

Amaze Holdings, Inc. is an end-to-end, creator-powered commerce platform offering tools for seamless product creation, advanced e-commerce solutions, and scalable managed services. By empowering anyone to “sell anything, anywhere,” Amaze enables creators to tell their stories, cultivate deeper audience connections, and generate sustainable income through shoppable, authentic experiences. Discover more at www.amaze.co.

Cautionary Note Regarding Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of Section 27A of the Securities Act and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”). These statements relate to future events and developments or to our future operating or financial performance, are subject to risks and uncertainties and are based estimates and assumptions. Forward-looking statements may include, but are not limited to, statements about the reverse stock split, our market opportunity and potential growth of that market, strategies, initiatives, growth, revenues, expenditures, our plans and objectives for future operations, and future financial and business performance. These statements can be identified by words such as such as “may,” “might,” “should,” “would,” “could,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “potential” or “continue,” and are based our current expectations and views concerning future events and developments and their potential effects on us.

These statements are subject to known and unknown risks, uncertainties and assumptions that could cause actual results to differ materially from those projected or otherwise implied by the forward-looking statement. These risks include: our ability to execute our plans and strategies; our limited operating history and history of losses; our financial position and need for additional capital; our ability to attract and retain our creator base and expand the range of products available for sale; we may experience difficulties in managing our growth and expenses; we may not keep pace with technological advances; there may be undetected errors or defects in our software or issues related to data computing, processing or storage; our reliance on third parties to provide key services for our business, including cloud hosting, marketing platforms, payment providers and network providers; failure to maintain or enhance our brand; our ability to protect our intellectual property; significant interruptions, delays or outages in services from our platform; significant data breach or disruption of the information technology systems or networks and cyberattacks; risks associated with international operations; general economic and competitive factors affecting our business generally; changes in laws and regulations, including those related to privacy, online liability, consumer protection, and financial services; our dependence on senior management and other key personnel; and our ability to attract, retain and motivate qualified personnel and senior management.

Additional risks and uncertainties that could cause actual outcomes and results to differ materially from those contemplated by the forward-looking statements are included in our Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and other future filings and reports that we file with the Securities and Exchange Commission (SEC) from time to time. Given these risks and uncertainties, you should not place undue reliance on these forward-looking statements. Also, these forward-looking statements represent our estimates and assumptions only as of the date of the press release. Unless required by law, we undertake no obligation to update or revise any forward-looking statements to reflect new information or future events or developments.

SOURCE: Amaze Holdings, Inc.

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Clear Start Tax Urges Families and Entrepreneurs to Act Before IRS Liens Create Long-Term Financial Consequences

IRVINE, CA / ACCESS Newswire / June 18, 2025 / Many Americans think of back taxes as a personal issue, but according to Clear Start Tax, the financial consequences can reach far beyond the individual. The national tax resolution firm is warning that unpaid tax debt can lead to aggressive IRS collection action, including federal tax liens, that may block property sales, impact business operations, and even interfere with a family’s ability to inherit property or assets.

As the IRS streamlines enforcement and invests in automation, liens are being filed faster – and impacting more people than ever.

“People assume tax debt is between them and the IRS,” said the Head of Client Solutions at Clear Start Tax. “But a lien follows you. It can block financing, derail business deals, and even affect your family’s ability to inherit what you leave behind.”

What Is a Federal Tax Lien – and Why It’s a Hidden Threat

Federal tax liens are one of the most powerful enforcement tools the IRS has. Once filed, a lien becomes public record and attaches to virtually everything the taxpayer owns, present and future. That includes homes, business assets, vehicles, and even financial accounts. Clear Start Tax says many people don’t fully understand the ripple effect a lien can have on both daily life and long-term goals.

Here are some of the key ways a federal tax lien can disrupt a taxpayer’s financial stability:

• Damaging credit scores, which limits access to mortgages, personal loans, or business funding

• Blocking property sales or refinancing, since the IRS has a legal claim over the asset

• Interfering with business operations, especially when assets are used as collateral

• Delaying or diminishing inheritance, because IRS liens must be satisfied before assets are transferred

By answering a few simple questions, taxpayers can find out if they’re eligible for the IRS Fresh Start Program and take the first step toward resolving their tax debt

Why Families and Business Owners Should Be Especially Cautious

While anyone can be affected by a tax lien, Clear Start Tax notes that families with estate plans and entrepreneurs with business holdings face the most serious consequences. These groups often have the most to lose if enforcement escalates.

Taxpayers in the following situations are particularly vulnerable:

• Business owners who rely on credit, property, or cash flow for daily operations

• Homeowners who need to refinance, sell, or use equity in their property

• Parents or grandparents looking to leave assets or property to their heirs

• Joint property owners who may be impacted, even if only one person has the tax debt

“Liens don’t just affect today’s finances,” said the Head of Client Solutions. “They can quietly erode tomorrow’s plans.”

How Clear Start Tax Helps Prevent or Resolve Federal Liens

The firm takes a proactive, client-centered approach to resolving tax debt before it leads to a lien – or to negotiate the removal of liens already filed. Clear Start Tax works directly with the IRS to protect clients’ assets and help them regain control of their financial future.

Their approach includes:

• Conducting thorough financial reviews to determine risk and eligibility for relief

• Creating personalized resolution strategies, such as Installment Agreements or Offer in Compromise

• Filing lien withdrawal or release requests, based on payment, hardship, or compliance

• Providing ongoing compliance support to prevent future liens or enforcement actions

Why Now Is the Time to Act

Clear Start Tax emphasizes that the best time to act is before a lien is filed. Once the IRS files a lien, the consequences grow quickly, and reversing the damage takes more time, paperwork, and cost. Whether you’re trying to protect a home, a business, or your family’s inheritance, waiting only increases the risk.

“Tax debt can create a domino effect that disrupts multiple generations if it’s not addressed early,” said the Head of Client Solutions. “We help people break that cycle before it gets written into the public record.”

About Clear Start Tax

Clear Start Tax is a full-service tax liability resolution firm that serves taxpayers throughout the United States. The company specializes in assisting individuals and businesses with a wide range of IRS and state tax issues, including back taxes, wage garnishment relief, IRS appeals, and offers in compromise. Clear Start Tax helps taxpayers apply for the IRS Fresh Start Program, providing expert guidance in tax resolution. Fully accredited and A+ rated by the Better Business Bureau, the firm’s unique approach and commitment to long-term client success distinguish it as a leader in the tax resolution industry.

Need Help With Back Taxes?

Click the link below:
https://clearstarttax.com/qualifytoday/
(888) 710-3533

Contact Information

Clear Start Tax
Corporate Communications Department
seo@clearstarttax.com
(949) 535-1627

SOURCE: Clear Start Tax

View the original press release on ACCESS Newswire

Regulatory Approval by the UK Financial Conduct Authority was Key Requirement for Transaction Timing

Minimal Conditions Remain for Deal Completion; Closing Expected in July, 2025

AUSTIN, TX AND NOTTINGHAM, UK / ACCESS Newswire / June 18, 2025 / Interactive Strength Inc. (NASDAQ:TRNR) (“TRNR” or the “Company”) today announced that it has received formal approval from the UK Financial Conduct Authority (“FCA”) for its previously-announced acquisition of Wattbike, the UK-based, omni-channel, connected, indoor-performance bike business, and that it expects to complete the acquisition in July, 2025.

The FCA’s approval satisfies a key condition for the closing of the acquisition, which is expected to significantly expand Interactive Strength Inc.’s presence in the global fitness market, particularly in the UK, and enhance its product offerings with a leading indoor-performance bike offering. This strategic acquisition is anticipated to be immediately accretive to TRNR’s results and accelerate growth, especially in key markets like the US and Germany, leveraging TRNR’s global distribution network.

Wattbike delivered over $15 million in 2024 revenue and has built on its prestigious elite-sport base – including Olympic teams, Premier League clubs, major US sports teams and elite fitness facilities – to debut a much broader product portfolio that will allow its footprint to scale internationally as well as in the UK, its home market.

“We have been waiting to secure FCA approval in order to finalize the Wattbike deal and now we will push to completion quickly,” said Trent Ward, Founder & CEO of Interactive Strength. “This regulatory hurdle was the main closing requirement the timing of which we did not control. The remaining steps are largely administrative. We’re already well underway integrating and collaborating with Wattbike, and we look forward to accelerating from here. Wattbike’s elite heritage, combined with TRNR’s Nasdaq listing, US distribution reach, and marketing muscle, positions us to drive meaningful growth across the UK, US, and Germany.”

“We remain thrilled to become part of the TRNR family,” added Stephen Loftus, CEO of Wattbike. “With FCA approval secured, we’re on the road to fully leverage TRNR’s global platform to accelerate our consumer and commercial expansion and bring premium, data-driven indoor cycling to new audiences.”

Wattbike is renowned for its high-performance connected indoor bikes, with deep penetration into leading UK gyms and an expanding direct-to-consumer customer base. The acquisition consideration is structured as an all-stock transaction for 100% of Wattbike, and there is an earn-out component to align the business’ financial performance with TRNR valuation. Further details regarding the financial impact of the acquisition will be provided in our upcoming filings with the U.S. Securities and Exchange Commission.

TRNR Media Contact

john@sintercompany.com

TRNR Investor Contact

ir@interactivestrength.com

About Interactive Strength Inc.:

Interactive Strength Inc. produces innovative specialty fitness equipment and digital fitness services under two main brands: 1) CLMBR and 2) FORME. Interactive Strength Inc. is listed on NASDAQ (symbol: TRNR).

CLMBR is a vertical climbing machine that offers an efficient and effective full-body strength and cardio workout. CLMBR’s design is compact and easy to move – making it perfect for commercial or in-home use. With its low impact and ergonomic movement, CLMBR is safe for most ages and levels of ability and can be found at gyms and fitness studios, hotels, and physical therapy facilities, as well as available for consumers at home. www.clmbr.com.

FORME is a digital fitness platform that combines premium smart gyms with live virtual personal training and coaching to deliver an immersive experience and better outcomes for both consumers and trainers. FORME delivers an immersive and dynamic fitness experience through two connected hardware products: 1) The FORME Studio Lift (fitness mirror and cable-based digital resistance) and 2) The FORME Studio (fitness mirror). In addition to the company’s connected fitness hardware products, FORME offers expert personal training and health coaching in different formats and price points through Video On-Demand, Custom Training, and Live 1:1 virtual personal training. www.formelife.com.

Forward Looking Statements:

This press release includes certain statements that are “forward-looking statements” for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements do not relate strictly to historical or current facts and reflect management’s assumptions, views, plans, objectives and projections about the future. Forward-looking statements generally are accompanied by words such as “believe”, “project”, “expect”, “anticipate”, “estimate”, “intend”, “strategy”, “future”, “opportunity”, “plan”, “may”, “should”, “will”, “would”, “will be”, “will continue”, “will likely result” or similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding the possibility of completing this acquisition in July or at all, the business being accretive to earnings, accelerating growth in the UK, US or Germany. The reader is cautioned not to rely on these forward-looking statements. These statements are based on current expectations of future events. If underlying assumptions prove inaccurate or known or unknown risks or uncertainties materialize, actual results could vary materially from the expectations and projections of the Company. Risks and uncertainties include but are not limited to: whether ATW Partners and / or DWF Labs will invest further amounts, other US publicly listed companies’ crypto strategies, and the price of $FET tokens. A further list and descriptions of these risks, uncertainties and other factors can be found in filings with the Securities and Exchange Commission. To the extent permitted under applicable law, the Company assumes no obligation to update any forward-looking statements.

# # #

SOURCE: Interactive Strength Inc.

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E-Motion™ 180E systems now eligible for up to $170,000 in per-unit government vouchers-driving large-scale electrification of commercial fleets in California

Key Highlights

• Vision Marine’s E-Motion™ 180E propulsion kits approved under California’s CORE (Clean Off-Road Equipment) program

• Up to $170,000 per vessel in state-funded vouchers available for qualifying fleet operators

• Applies to both new electric boat builds and retrofit conversions using Vision Marine’s certified installers

• California market includes approximately 4,400 commercially operated vessels across sectors such as ferries, harbor patrol, tour boats, rentals, and service craft

• Approval aligns with broader industry momentum toward electrification, strengthening Vision Marine’s market position

MONTREAL, QC / ACCESS Newswire / June 18, 2025 / Vision Marine Technologies Inc. (NASDAQ:VMAR), a developer of high-performance electric marine propulsion systems, announced today that its flagship E-Motion™ 180E powertrain has been approved for inclusion in California’s CORE (Clean Off-Road Equipment) Voucher Incentive Project.

This approval makes Vision Marine’s propulsion kits eligible for point-of-sale vouchers of up to $170,000 per unit, substantially reducing the cost of adopting electric propulsion for organizations modernizing their fleets.

“This represents a major milestone for Vision Marine, significantly enhancing our market position and accelerating our ability to drive widespread adoption of electric propulsion technology,” said Alexandre Mongeon, CEO of Vision Marine Technologies.

California: A Strategic Market for Marine Electrification

California operates one of the largest and most dynamic commercially operated marine sectors in North America. With approximately 4,400 vessels in use across ferry services, water taxis, harbor patrol, tour operations, and rental businesses, the state presents a significant opportunity for electrification. Many of these segments are actively seeking clean alternatives to gas and diesel propulsion due to emissions regulations and increasing demand for quieter, lower-maintenance vessels.

Vision Marine’s E-Motion™ 180E system-now listed under CORE-offers a compliant, high-performance solution for operators upgrading existing boats or commissioning new electric vessels.

Market Impact and Sales Potential

With this approval, Vision Marine can now offer its E-Motion™ 180E propulsion kits to eligible buyers with substantial financial support from the CORE program. Both new electric vessels and repower conversions are supported when completed by certified Vision Marine technicians and installers.

As the only 180 HP continuous electric powertrain listed under CORE, Vision Marine stands to benefit from increased demand across a wide range of commercial use cases. The company’s commercial readiness, field-tested product, and established presence in California position it well to respond to immediate regional fleet electrification needs.

This milestone also comes as the global marine industry rapidly shifts toward clean propulsion. The combination of policy-driven funding and organic market demand creates a powerful tailwind for Vision Marine Technologies.

“California has long been a bellwether for clean technology adoption,” added Mongeon. “Our CORE approval enhances our visibility and competitiveness in this key market, while reinforcing our ability to scale as electrification expands across North America.”

About Vision Marine Technologies Inc.

Vision Marine Technologies Inc. (NASDAQ:VMAR) is a leader in high-performance electric marine propulsion. Its flagship E-Motion™ 180E system delivers 180 HP of continuous power through a fully integrated, scalable electric powertrain platform. Built for reliability and commercial-grade use, Vision Marine’s solutions serve OEMs, fleet operators, government agencies, and rental services across North America.

For more information, visit: www.visionmarinetechnologies.com

About the CORE Program

The Clean Off-Road Equipment (CORE) Voucher Incentive Project is administered by the California Air Resources Board (CARB) and funded by the state’s Cap-and-Trade program. CORE provides point-of-sale vouchers that help reduce the upfront cost of zero-emission off-road equipment, including marine technologies. The program is designed to accelerate the adoption of cleaner equipment and support California’s climate and air quality goals.

To learn more, visit: www.californiacore.org

Forward-Looking Statements

Certain statements in this press release, including, but not limited to, statements regarding the anticipated benefits of the exclusive supply agreement, market expansion, and future events, are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements are based on assumptions and subject to various risks and uncertainties that could cause actual results to differ materially from those expressed or implied in such statements. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. Vision Marine disclaims any obligation to update these statements except as required by law. Actual results may differ materially from those expressed or implied. For a detailed discussion of these risks, refer to Vision Marine’s Annual Report on Form 20-F for the year ended August 31, 2024, and other periodic filings with the SEC. Vision Marine does not undertake any obligation to update or revise forward-looking statements other than as required by law.

Investor Relations Contact:

Vision Marine Technologies Inc.
Bruce Nurse – Investor Relations
bn@v-mti.com
(303) 919-2193

Website: visionmarinetechnologies.com
Twitter: @marine_vision
Facebook: @VisionMarineTechnologies
Instagram: @visionmarine.technologies
YouTube: @VisionMarineTechnologies

SOURCE: Vision Marine Technologies Inc

View the original press release on ACCESS Newswire

TORONTO, ON AND BREDA, THE NETHERLANDS / ACCESS Newswire / June 18, 2025 / Organto Foods Inc. (TSXV:OGO)(OTC PINK:OGOFF) (“Organto” or the “Company“) today announced it plans to complete a non-brokered private placement of up to 4,000,000 units of the Company (the “Units”) at a price of $0.25 per Unit (the “Private Placement“), with each Unit consisting of one Common Share in the capital of the Company (a “Common Share“) and one-half common share purchase warrant of the Company (a “Warrant“).

Each full Warrant shall entitle the holder thereof to acquire one Common Share (a” Warrant Share“) at a price per Warrant Share of C$0.35 for a period of 18 months from the closing date of the Private Placement.

“We’re very pleased with our operational performance, having realized first quarter sales growth of 193.5%, gross profit dollar growth of 298.1%, our lowest cash operating costs as a percentage of sales in our history and our first-ever positive EBITDA quarter. Our business has continued to accelerate through the second quarter, which is quite encouraging, and we believe is a reflection of the strong momentum in our business. These results are the direct outcome of the extensive restructuring and strategic realignment we’ve executed over the past 18 months, laying a solid foundation for sustained growth, stability, and a clear path to profitability. With our continued growth and improvement in our share price, we believe it is prudent to complete this Private Placement as we conservatively manage our balance sheet.” commented Steve Bromley, Chair and Chief Executive Officer.

The Company may pay finders’ fees in connection with the Private Placement. The net proceeds from the Private Placement will be used to fund general working capital.

Certain directors and officers of the Company may acquire securities under the Private Placement. Any such participation would be considered to be a “related party transaction” as defined under Multilateral Instrument 61-101 (“MI 61-101“). The transaction will be exempt from the formal valuation and minority shareholder approval requirements of MI 61-101 as neither the fair market value of any units issued to or the consideration paid by such persons will exceed 25% of the Company’s market capitalization.

Completion of the Private Placement will be subject to the prior approval of the TSX Venture Exchange as well as all other requisite corporate, regulatory and security holder approvals, as applicable. Further, all securities issued pursuant to the Private Placement described above will be subject to a minimum hold period of four months and one day from their date of issuance. There can be no assurance that the Company will be successful in completing the Private Placement.

ON BEHALF OF THE BOARD

Steve Bromley
Chairman and CEO

For more information, contact:

Investor Relations
John Rathwell, Senior Vice President, Investor Relations & Corporate Development
647 629 0018
info@organto.com

ABOUT ORGANTO

Organto is a leading provider of branded, private label, and distributed organic and non-GMO fruit and vegetable products using a strategic asset-lighter business model to serve a growing socially responsible and health-conscious consumers. Organto’s business model is rooted in its commitment to sustainable business practices focused on environmental responsibility and a commitment to the communities where it operates, its people, and its shareholders.

FORWARD LOOKING STATEMENTS

This news release may include certain forward-looking information and statements, as defined by law, including without limitation, Canadian securities laws and the “safe harbor” provisions of the US Private Securities Litigation Reform Act (“forward-looking statements”). In particular, and without limitation, this news release contains forward-looking statements respecting Organto’s business model and markets; Organto’s belief that the Company has made solid progress in the restructuring and realignment of its business focused on a clear path to profitability, sustained growth and long-term stability; Organto’s belief that the impact of restructuring and realignment efforts was a key driver of its first quarter results; and Organto’s belief it is prudent to complete this Private Placement as the Company conservatively manages its balance sheet. Forward-looking statements are based on a number of assumptions that may prove to be incorrect, including, without limitation, the assumption that the Company will be able to complete the Private Placement and obtain all regulatory and requisite approvals in a timely manner and on acceptable terms. There can be no assurance that forward-looking statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on forward-looking statements. Factors that could cause actual results to differ materially from those anticipated in forward-looking statements in this news release include, among others, regulatory risks; risks related to market volatility and economic conditions; risks related to unforeseen delays; and risks that necessary financing will be unavailable when needed. For further information on these and other risks and uncertainties that may affect the Company’s business, see the “Risks and Uncertainties” and “Forward-Looking Statements” sections of the Company’s annual and interim management’s discussion and analysis filings with the Canadian securities regulators, which are available under the Company’s profile at www.sedarplus.ca. Except as required by law, Organto does not assume any obligation to release publicly any revisions to forward-looking statements contained in this news release to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this news release.

SOURCE: Organto Foods, Inc.

View the original press release on ACCESS Newswire

SHELTON, CT / ACCESS Newswire / June 18, 2025 / Dr. Anil Diwan, President of NanoViricides, Inc. (NYSE Amer.: NNVC ) (the “Company”), asserts that with new rising variants of COVID and Bird Flu, the single broad-spectrum antiviral drug NV-387 is well-positioned to support preparedness efforts and to combat potential pandemics.

Nimbus, a new COVID variant, officially NB1.8.1, is displacing the LP8.1 variant that was dominant until a few weeks ago in the USA (https://www.today.com/health/coronavirus/new-covid-variant-nb181-nimbus-symptoms-rcna212304).

Nimbus has been rising globally since Spring according to WHO (https://cdn.who.int/media/docs/default-source/documents/epp/tracking-sars-cov-2/23052025_nb.1.8.1_ire.pdf).

Nimbus causes “razor-sharp” sore throat in some individuals, which is extremely painful and lingering for some time, in addition to the usual COVID symptoms.

Nimbus is more resistant to antibodies generated from previous vaccines, although prior vaccination or natural COVID infection is expected to still be protective in terms reduced severity compared to without such immunity according to CDC.

Nimbus is likely to be more transmissible than the previous variants. It belongs to the JN.1 subfamily of the Omicron family of SARS-CoV-2 virus.

Recently, the Influenza A H5N1 virus from a dairy worker in Michigan was found to be capable of airborne transmission in a ferret animal model ^[1] (https://www.freep.com/story/news/health/2025/06/05/h5n1-bird-flu-michigan-dairy-farm-airborne-spread-cdc-study/84046550007/). This genotype B3.13 (clade clade 2.3.4.4b) virus in dairy cattle causes moderate severity disease in humans. In contrast, a highly pathogenic genotype D1.1 that is circulating in birds birds has led to one critical month-long illness in Canada and one death in the US signifying the potential for high morbidity and mortality from this genotype if it spreads in humans.

Additionally, a new genotype of H5N1 in Cambodia has caused four fatalities and fifth severe infection as of today (https://www.cidrap.umn.edu/avian-influenza-bird-flu/h5n1-avian-flu-infects-fifth-patient-cambodia).

NV-387, the broad-spectrum antiviral drug is expected to be effective against all of these bird flu viruses. NV-387 was found to be substantially superior to Tamiflu® (Roche, Oseltamivir), Rapivab® (Biocryst, Peramivir), as well as Xofluza (Shionogi/Roche, baloxavir) in lethal lung infection animal model of Influenza infection. All three of these existing anti-influenza drugs are known to be escaped by Influenza viruses by single point mutations in H or PB2 genes.

NV-387 was found to be substantially superior to the approved drug Remdesivir in a lethal coronavirus lung infection animal model for SARS-CoV-2.

Thus the single drug NV-387 alone can combat H5N1, Influenza as well as COVID infections.

NV-387 has completed Phase I clinical trial in healthy human subjects with no reported adverse events.

COVID as well as Influenza viruses readily escape vaccines, antibodies as they change in the field during an epidemic wave. They are also likely to escape small molecule drugs by such changes.

NV-387 takes advantage of the invariant features that these viruses use for causing infection, by mimicking heparan sulfate-like structures. No matter how much these viruses change in the field, they continue to use the heparan sulfate attachment receptors in order to cause infection. Thus it is practically impossible that the viruses may be able escape NV-387 without losing their ability infect and transmit across humans, the Company believes.

NV-387 is orally available, formulated as oral gummies that dissolve in the mouth, thus avoiding issues of inability to swallow which occurs related to sore throat, old age, as well as in young children.

NV-387, as a treatment, is designed to help actually patients with disease recover rapidly, thus limiting the viral spread as well as providing for natural infection-based immunity in the recovered patient.

“NV-387 is thus the best current choice available for a highly cost-effective pandemic preparedness development,” said Anil R. Diwan, PhD, President and Executive Chairman of the Company, adding, “We have US-based cGMP manufacturing capabilities already set up as well.”

Of note, natural immunity, as induced by recovery from infection, is known to be superior to immunity from subunit and mRNA vaccines. One of the important reasons is that in natural infection, the immune system is subjected to all possible antigens from the entire virus, unlike just the selected antigens or antigen fragments that are present in subunit or mRNA vaccines.

Also, NV-387 can be manufactured in the USA and stockpiled readily at room temperature or refrigeration (for longer periods of time).

Unlike NV-387, vaccines or antibodies would require to be created after the virus takes hold, and they would suffer substantial loss of effectiveness within months after deployment due to changes in the virus. Additionally, vaccines require a cold chain handling. Vaccines also need to be administered to a large proportion of healthy population. There are significant logistical problems with vaccines. There is also the issue of vaccine reluctance, which is a personal choice, as it should be in a free country like the USA.

The broad-spectrum antiviral drug NV-387 was developed specifically to overcome all of these problems. In case of further spread of a severe COVID variant and also a Bird Flu variant in human populations, it will be possible to move NV-387 rapidly into Phase II clinical trial for these diseases, and then prepare for deployment early in the potential pandemic, curtailing its spread.

About NanoViricides

NanoViricides, Inc. (the “Company”) (www.nanoviricides.com) is a clinical stage company that is creating special purpose nanomaterials for antiviral therapy. The Company’s novel nanoviricide™ class of drug candidates and the nanoviricide™ technology are based on intellectual property, technology and proprietary know-how of TheraCour Pharma, Inc. The Company has a Memorandum of Understanding with TheraCour for the development of drugs based on these technologies for all antiviral infections. The MoU does not include cancer and similar diseases that may have viral origin but require different kinds of treatments.

The Company has obtained broad, exclusive, sub-licensable, field licenses to drugs developed in several licensed fields from TheraCour Pharma, Inc. The Company’s business model is based on licensing technology from TheraCour Pharma Inc. for specific application verticals of specific viruses, as established at its foundation in 2005.

Our lead drug candidate is NV-387, a broad-spectrum antiviral drug that we plan to develop as a treatment of RSV, COVID, Long COVID, Influenza, and other respiratory viral infections, as well as MPOX/Smallpox infections. Our other advanced drug candidate is NV-HHV-1 for the treatment of Shingles. The Company cannot project an exact date for filing an IND for any of its drugs because of dependence on a number of external collaborators and consultants. The Company is currently focused on advancing NV-387 into Phase II human clinical trials.

NV-CoV-2 (API NV-387) is our nanoviricide drug candidate for COVID-19 that does not encapsulate remdesivir. NV-CoV-2-R is our other drug candidate for COVID-19 that is made up of NV-387 with remdesivir encapsulated within its polymeric micelles. The Company believes that since remdesivir is already US FDA approved, our drug candidate encapsulating remdesivir is likely to be an approvable drug, if safety is comparable. Remdesivir is developed by Gilead. The Company has developed both of its own drug candidates NV-CoV-2 and NV-CoV-2-R independently.

The Company is also developing drugs against a number of viral diseases including oral and genital Herpes, viral diseases of the eye including EKC and herpes keratitis, H1N1 swine flu, H5N1 bird flu, seasonal Influenza, HIV, Hepatitis C, Rabies, Dengue fever, and Ebola virus, among others. NanoViricides’ platform technology and programs are based on the TheraCour® nanomedicine technology of TheraCour, which TheraCour licenses from AllExcel. NanoViricides holds a worldwide exclusive perpetual license to this technology for several drugs with specific targeting mechanisms in perpetuity for the treatment of the following human viral diseases: Human Immunodeficiency Virus (HIV/AIDS), Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Rabies, Herpes Simplex Virus (HSV-1 and HSV-2), Varicella-Zoster Virus (VZV), Influenza and Asian Bird Flu Virus, Dengue viruses, Japanese Encephalitis virus, West Nile Virus, Ebola/Marburg viruses, and certain Coronaviruses. The Company intends to obtain a license for RSV, Poxviruses, and/or Enteroviruses if the initial research is successful. As is customary, the Company must state the risk factor that the path to typical drug development of any pharmaceutical product is extremely lengthy and requires substantial capital. As with any drug development efforts by any company, there can be no assurance at this time that any of the Company’s pharmaceutical candidates would show sufficient effectiveness and safety for human clinical development. Further, there can be no assurance at this time that successful results against coronavirus in our lab will lead to successful clinical trials or a successful pharmaceutical product.

This press release contains forward-looking statements that reflect the Company’s current expectation regarding future events. Actual events could differ materially and substantially from those projected herein and depend on a number of factors. Certain statements in this release, and other written or oral statements made by NanoViricides, Inc. are “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. You should not place undue reliance on forward-looking statements since they involve known and unknown risks, uncertainties and other factors which are, in some cases, beyond the Company’s control and which could, and likely will, materially affect actual results, levels of activity, performance or achievements. The Company assumes no obligation to publicly update or revise these forward-looking statements for any reason, or to update the reasons actual results could differ materially from those anticipated in these forward-looking statements, even if new information becomes available in the future. Important factors that could cause actual results to differ materially from the company’s expectations include, but are not limited to, those factors that are disclosed under the heading “Risk Factors” and elsewhere in documents filed by the company from time to time with the United States Securities and Exchange Commission and other regulatory authorities. Although it is not possible to predict or identify all such factors, they may include the following: demonstration and proof of principle in preclinical trials that a nanoviricide is safe and effective; successful development of our product candidates; our ability to seek and obtain regulatory approvals, including with respect to the indications we are seeking; the successful commercialization of our product candidates; and market acceptance of our products.

The phrases “safety”, “effectiveness” and equivalent phrases as used in this press release refer to research findings including clinical trials as the customary research usage and do not indicate evaluation of safety or effectiveness by the US FDA.

FDA refers to US Food and Drug Administration. IND application refers to “Investigational New Drug” application. cGMP refers to current Good Manufacturing Practices. CMC refers to “Chemistry, Manufacture, and Controls”. CHMP refers to the Committee for Medicinal Products for Human Use, which is the European Medicines Agency’s (EMA) committee responsible for human medicines. API stands for “Active Pharmaceutical Ingredient”. WHO is the World Health Organization. R&D refers to Research and Development.

Contact:
NanoViricides, Inc.
info@nanoviricides.com

Public Relations Contact:
ir@nanoviricides.com

---

SOURCE: NanoViricides, Inc.

View the original press release on ACCESS Newswire

NEW YORK CITY, NY / ACCESS Newswire / June 17, 2025 / Influencer Luke Parry and entrepreneur Andrea Harris Jr. have officially announced a strategic business partnership that aims to reshape the digital landscape. With plans to launch a series of ventures spanning fashion, social technology and influencer marketing, the duo intends to capitalize on some of the fastest-growing sectors in today’s economy.

The collaboration marks a significant milestone for both Parry and Harris Jr., combining creative influence with operational expertise to build what they describe as “a portfolio of brands designed for the future of consumer behavior.”

A Digital-Era Alliance

Parry, known for his cinematic content, emotional storytelling and influential presence across social platforms, brings a powerful cultural pulse to the partnership. Harris Jr., a strategist and product developer with a background in early-stage startups and brand architecture, brings the operational clarity and business infrastructure necessary to scale quickly.

“We’re not just launching products-we’re launching ecosystems,” Harris Jr. said. “Everything we do is designed to connect, convert and cultivate long-term consumer relationships.”

The partnership will center around three key verticals: fashion, dating and digital influence. Each reflects both the cultural relevance of their personal brands and the broader economic trends fueling growth in these industries.

Targeting High-Growth Markets

The fashion sector is expected to exceed $1.2 trillion globally by 2027, with significant growth coming from direct-to-consumer models, gender-fluid design and sustainability-focused brands. Parry and Harris Jr. intend to leverage this momentum by launching a fashion brand that centers individuality, self-expression and eco-conscious production.

“The fashion industry is overdue for reinvention,” Parry said. “Consumers want transparency, story and design they can see themselves in. We’re going to deliver that.”

Equally high on their agenda is the dating and relationship technology space, which has seen explosive demand in recent years. According to Statista, the global online dating market is projected to surpass $12 billion by 2030, fueled by younger users seeking more personalized, secure and experience-driven platforms.

Parry and Harris Jr. plan to launch a new dating app that focuses on compatibility, conversation and community-pushing back against the often impersonal swipe-based culture of traditional apps.

“We’re creating something that fosters genuine connection,” Harris Jr. said. “This isn’t gamification. It’s human-first technology.”

Influencer Marketing 2.0

In addition to launching consumer-facing products, the pair intends to build out a new model for influencer marketing-one that prioritizes authenticity, long-term partnerships and co-creation.

With global influencer marketing spend projected to reach $32 billion by 2026, they see an opportunity to set a new standard. The partnership includes plans to develop proprietary tools that connect creators with brands through transparent, equity-based relationships.

“We understand this space from both sides,” Parry said. “We’ve been the talent. We’ve built the content. Now we’re building the infrastructure.”

The goal is to support emerging influencers while also helping legacy brands connect to new audiences more effectively.

Designed for Longevity

While the ventures are still in early stages, both founders emphasized that the long-term vision is to build enduring brands-not momentary hype.

Each business under their collaboration will follow a phased launch strategy, with beta testing and community involvement playing a central role in development. The duo has already begun assembling a cross-disciplinary advisory team of technologists, designers and brand operators.

“We’re playing the long game,” Harris Jr. said. “This is about solving real problems and building value at scale.”

Consumer-Centric, Value-Driven

Whether in fashion, dating or digital influence, the partners share a deep focus on user experience, ethical practices and cultural relevance. They aim to build not just brands-but belief systems that consumers can trust and participate in.

By staying agile and focused on underserved markets, they believe they can create category-defining experiences that resonate with a new generation of consumers.

Looking Ahead

As anticipation builds, Parry and Harris Jr. will spend the next several months developing brand strategy, platform infrastructure and early partnerships ahead of phased launches beginning in 2026.

Public announcements and product previews are expected later this year, with early access opportunities available to subscribers through their forthcoming platform.

“This is the future of brand-building,” Parry said. “It’s bold. It’s personal. And it’s just the beginning.”

About Luke Parry
Luke Parry is a digital creator and cultural voice known for his emotional storytelling and distinctive visual style. His content has garnered a loyal following across multiple platforms, and he is widely regarded as one of the next-generation leaders in content-driven commerce.

About Andrea Harris Jr.
Andrea Harris Jr. is an entrepreneur, strategist and advisor with a background in building scalable businesses across technology, fashion and consumer marketing. He specializes in brand incubation, digital infrastructure and venture growth.

Contact:

Jake Bodiford
mgmt@northregia.com

SOURCE: Harris & Parry LLP

View the original press release on ACCESS Newswire

Need a Ride to Your Medical Appointment? Diamond Care Transportation Offers Safe, On-Time NEMT Services for Seniors and Disabled Patients in South Carolina

GREENVILLE, SOUTH CAROLINA / ACCESS Newswire / June 17, 2025 / Diamond Care Transportation is proud to offer safe, reliable, and wheelchair-accessible Non-Emergency Medical Transportation (NEMT) for seniors, disabled individuals, and patients who need help getting to medical appointments. Based in South Carolina, Diamond Care is now serving Florida, Maryland, and Washington, D.C., as well.

If you or a loved one needs a ride to a doctor’s office, hospital, physical therapy, dialysis center or clinic, Diamond Care makes it easy. No long wait times, no confusion – just caring drivers, clean vehicles, and dependable service you can count on.

What We Offer:

• Wheelchair-accessible vehicles for any mobility level

• Friendly, trained, and CPR-certified drivers

• On-time pickup and drop-off

• Recurring or one-time ride options

• Service from home, nursing home or medical facility

“We believe no one should miss medical care because they can’t get there,” said a representative from Diamond Care. “That’s why we go above and beyond to make sure every patient arrives safely and on time – with care, dignity, and comfort.”

Now Booking NEMT Rides in:

• South Carolina (including Greenville, Columbia, and Charleston)

• Florida (Miami, Tampa, Orlando, Jacksonville)

• Washington State (Seattle, Spokane, Tacoma)

• Maryland (Baltimore, Rockville, Silver Spring)

• Washington, D.C.

Whether it’s a regular appointment or an urgent follow-up, Diamond Care is your partner in health transportation. We help seniors and individuals with disabilities get the care they need – without stress.

Need a Non Emergency Medical Ride to the Doctor? Diamond Care Transportation is Here to Help!

Ready to Book a Ride?

Call Now: +1 (864) 335-9824
Email: info@diamondcaretransportation.com
Website: https://diamondcaretransportation.com

We’re available to answer questions and schedule rides – whether it’s for tomorrow or next week. Let Diamond Care Transportation help you get there safely.

About Diamond Care Transportation

Diamond Care Transportation provides Non-Emergency Medical Transportation (NEMT) with a focus on wheelchair transport, senior care, and disability support. We proudly serve patients across South Carolina, Florida, Washington, Maryland, and D.C., offering trusted service that puts your comfort and health first.

CONTACT: info@diamondcaretransportation.com

SOURCE: Diamond Care Transportation

View the original press release on ACCESS Newswire