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  • Cameron Ashley Expands Florida Presence With New Jacksonville Distribution Center

    Cameron Ashley Expands Florida Presence With New Jacksonville Distribution Center

    GREENVILLE, SOUTH CAROLINA / ACCESS Newswire / November 13, 2025 / Cameron Ashley Building Products (Cameron Ashley) has opened a new distribution center in Jacksonville, Florida, strengthening its service capabilities across North Florida and Georgia’s coastal markets.

    This strategic expansion gives customers faster, more reliable access to a full suite of residential and light commercial building products, helping them keep projects on schedule and customers satisfied.

    The Jacksonville facility is a core market location, stocking Roofing, Gypsum, Insulation, and all related accessories. Cameron Ashley delivers convenience, speed, and local expertise to meet growing demand in one of the Southeast’s fastest-growing construction markets.

    “This new Jacksonville facility enhances our statewide network, allowing us to deliver faster and more reliably across Florida,” said John Gambone, Regional Vice President. “By stocking our Core 3 products, we’re giving customers the tools they need to compete and win – backed by same-day or next-day delivery and the product knowledge and service they expect from Cameron Ashley.”

    The new facility will be led by Distribution Center Manager Mark Mixon, a veteran professional in the roofing and insulation industries. “With years of experience supporting customers in this region, I understand their challenges,” said Mixon. “Our Jacksonville team knows the products, knows the market, and is ready to deliver the fast, dependable service customers deserve.”

    With Jacksonville now online, Cameron Ashley operates a growing network of Florida distribution centers in Lakeland, Fort Pierce, and Fort Myers, ensuring statewide coverage and next-day delivery to nearly every major metro area.

    The Jacksonville Distribution Center is located at 2210 Melson Avenue, Suite 101, Jacksonville, FL 32254, and can be reached at 904-807-2919.

    About Cameron Ashley Building Products, Inc.

    Cameron Ashley is a leading wholesale distributor of roofing, insulation, gypsum, siding, and other specialty building products. We deliver a premier portfolio of nationally recognized brands to customers across the lumber and building materials industry.

    With more than 70 distribution centers nationwide, we stock large volumes of building products locally and offer flexible, customer-centric delivery options through our F^ST same-day or next-day delivery platforms.

    Our relationship-driven approach includes the industry-leading PLUS® Points loyalty program, free merchandising support, as well as exclusive purchasing and show incentives. Customers can shop anytime through either our CONNECT online portal or mobile app, which provide real-time access to product availability, pricing, order history, secure payments, and detailed product specs and warranties.

    To learn more or place an order, visit cameronashleybp.com.

    Contact Information

    Sara Eller
    VP Marketing
    saraeller@cameronashleybp.com
    864-281-3687

    .

    SOURCE: Cameron Ashley Building Products

    View the original press release on ACCESS Newswire

  • Jaguar Health Provides Recap of November 8, 2025 Presentation on Groundbreaking Results of Proof-of-Concept Study of Crofelemer for Treatment of Pediatric Intestinal Failure at NASPGHAN Annual Meeting

    Jaguar Health Provides Recap of November 8, 2025 Presentation on Groundbreaking Results of Proof-of-Concept Study of Crofelemer for Treatment of Pediatric Intestinal Failure at NASPGHAN Annual Meeting

    Crofelemer can potentially extend and save lives of microvillus inclusion disease patients, reducing the volume of the total parenteral support (PS) necessary for them to survive

    Groundbreaking PS reduction of up to 37% is unprecedented; No approved treatments exist for MVID

    SAN FRANCISCO, CA / ACCESS Newswire / November 13, 2025 / Jaguar Health, Inc. (NASDAQ:JAGX) (Jaguar) family company Napo Pharmaceuticals (Napo) today provided a recap of the November 8, 2025 presentation at the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) Annual Meeting describing the initial groundbreaking results of an independent investigator-initiated trial (IIT) of crofelemer in the UAE for treatment of pediatric intestinal failure, which includes patients with ‘intestinal failure’ due to microvillus inclusion disease (MVID) and short bowel syndrome (SBS-IF).

    “The intestines of patients with the ultrarare genetic disorder MVID do not function properly, as is often the case with patients having intestinal failure due to short bowel syndrome. The intestines of these patients are unable to absorb the fluids, electrolytes and nutrients required to survive and thrive. Intestinal failure is a debilitating, lifelong condition that often requires patients to receive life-sustaining fluids, electrolytes and nutrients through intravenous administration, which consists of total parenteral nutrition (TPN) with supplemental intravenous fluids, which together constitute parenteral support (PS). Most intestinal failure patients require PS up to 7 days a week, and sometimes for 20 hours or more per day,” said Lisa Conte, Jaguar’s founder, president, and CEO.

    While crucial for these patients, total parenteral support is associated with significant toxicities to patients, similar to some toxicities associated with chemotherapy, often causing serious health problems including infections, metabolic complications, liver and kidney function problems – as well as a risk of neurodevelopmental delay. These symptoms may emerge at any time in intestinal failure patients, and often become life-threatening.

    As presented at NASPGHAN, the results of this ongoing and independent proof-of-concept trial of crofelemer demonstrate disease progression modification through reduction of total parenteral support (PS) in pediatric intestinal failure patients that ranged from 12 to 37%. Specifically, in the two SBS-IF patients who have completed treatment, the results show crofelemer reduced PS between 12.5 to 15.6% at the highest dose over the 12-week treatment period, together with reduced loose watery stools frequency. For the initial MVID patient who has completed treatment, PS needs were reduced by up to 27% at the highest dose over the initial 12-week treatment period and up to 37% during the extension period upon reinitiation of crofelemer treatment, and also showed reduced frequency of loose watery stools. These findings support continued evaluation of crofelemer to reduce PS needs for pediatric intestinal failure patients.

    The presentation on November 8, 2025 at NASPGHAN, was titled Exploratory Single-Arm, Open-Label Non-Randomized Trial Evaluating the Safety and Effectiveness of Crofelemer in Pediatric Patients with Intestinal Failure. The study’s primary investigator, Dr. Mohamad Miqdady, Division Chief of the Pediatric Gastroenterology, Hepatology & Nutrition Division at Sheikh Khalifa Medical City (SKMC), a tertiary care center in Abu Dhabi in the UAE, described these initial findings in pediatric intestinal failure patients with crofelemer treatment.

    A recognized leader in pediatric gastroenterology, Dr. Miqdady is Professor of Pediatric Gastroenterology at Khalifa University’s medical school, and completed his Fellowship in Pediatric Gastroenterology at Baylor College of Medicine and Texas Children’s Hospital in Houston. He is a member of Napo’s Scientific Advisory Board.

    MVID is a devastating ultrarare pediatric disorder, with an estimated worldwide prevalence of 100-200 patients, characterized by severe malabsorption that requires life-sustaining parenteral support to meet the nutritional, fluid and electrolyte requirements of the child, and for which there are currently no approved treatments. MVID has a lethal natural history along with significant co-morbidities. Short bowel syndrome (SBS) affects approximately 10,000 to 20,000 people in the U.S., according to the Crohn’s & Colitis Foundation, and it is estimated that the population of SBS patients in Europe is approximately the same size.

    In addition to supporting the IIT in the UAE, Napo is also conducting the placebo-controlled clinical trial of crofelemer in pediatric MVID patients at sites in the U.S., E.U., and Middle East under appropriate regulatory approvals in each of these geographies. The company is also providing crofelemer powder for oral solution for use in two expanded access programs in intestinal failure patients the U.S. to treat adult and pediatric intestinal failure patients with short bowel syndrome and MVID, respectively.

    The mission of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) is to be a world leader in research, education, clinical practice and advocacy for pediatric gastroenterology, hepatology and nutrition in health and disease. NASPGHAN strives to improve the care of infants, children and adolescents with digestive disorders by promoting advances in clinical care, research and education.

    About the Jaguar Health Family of Companies

    Jaguar Health, Inc. (Jaguar) is a commercial stage pharmaceuticals company focused on developing novel proprietary prescription medicines sustainably derived from plants from rainforest areas for people and animals with gastrointestinal distress. Jaguar family companies Napo Pharmaceuticals (Napo) and Napo Therapeutics S.p.A. focus on the development and commercialization of novel crofelemer powder for oral solution for the treatment of rare and orphan gastrointestinal disorders with intestinal failure, including microvillus inclusion disease and short bowel syndrome.

    For more information about:

    Jaguar Health, visit https://jaguar.health

    Napo Pharmaceuticals, visit www.napopharma.com

    Napo Therapeutics, visit napotherapeutics.com

    Forward-Looking Statements

    Certain statements in this press release constitute “forward-looking statements.” These include statements regarding Jaguar’s expectation that crofelemer can potentially extend and save lives of MVID patients, reducing the volume of the PS necessary for them to survive. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “aim,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “potential” or “continue” or the negative of these terms or other similar expressions. The forward-looking statements in this release are only predictions. Jaguar has based these forward-looking statements largely on its current expectations and projections about future events. These forward-looking statements speak only as of the date of this release and are subject to several risks, uncertainties, and assumptions, some of which cannot be predicted or quantified and some of which are beyond Jaguar’s control. Except as required by applicable law, Jaguar does not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

    Contact:

    hello@jaguar.health
    Jaguar-JAGX

    SOURCE: Jaguar Health, Inc.

    View the original press release on ACCESS Newswire

  • AmeriLife Recognized as a 2025 Inc. Power Partner Award Winner for the Third Consecutive Year

    AmeriLife Recognized as a 2025 Inc. Power Partner Award Winner for the Third Consecutive Year

    The annual list recognizes the leading B2B companies that have proven track records of supporting entrepreneurs and helping companies grow

    CLEARWATER, FL / ACCESS Newswire / November 13, 2025 / AmeriLife, a national leader in life and health insurance distribution, wealth management, and retirement solutions, is proud to announce its recognition on the Inc. Power Partner Awards for the third consecutive year. The prestigious list honors B2B organizations that have proven track records of supporting entrepreneurs and helping startups grow. AmeriLife was recognized in the categories of General Excellence, Marketing Creativity & Branding, and Best United States Power Partner.

    “This incredible recognition is a testament to our team’s continued dedication to supporting entrepreneurs and helping businesses thrive,” said Scott Perry, Chairman and CEO of AmeriLife. “We’re honored to be acknowledged for achievements that reflect our commitment to providing exceptional service and support to our affiliate partners.”

    As a national leader in life and health insurance distribution, wealth management, and retirement solutions, AmeriLife’s partnership program has become a benchmark for independent and field marketing organizations seeking to expand their reach and resources without compromising operational control over their business. By partnering with AmeriLife, companies can leverage the firm’s extensive distribution network, advanced marketing capabilities, technology solutions, and regulatory compliance tools, allowing them to focus on their core business while driving growth.

    AmeriLife’s recent strategic moves have further strengthened its market position. In March, AmeriLife finalized its acquisition Crump Life Insurance Services, enhancing its wealth distribution capabilities within the institutional, IMO, and BGA segments. Crump’s expertise spans life insurance and retirement products, and it partners with over 31,000 financial professionals to deliver holistic solutions. This acquisition marked a significant step forward for AmeriLife, transforming its wealth distribution approach and delivering comprehensive, integrated solutions.

    AmeriLife, through its affiliate Saybrus Partners, also entered into a strategic partnership with SterlingBridge Insurance Agency, expanding its national reach and capabilities in life insurance and annuity distribution. This partnership demonstrates the ability for affiliates to access capital and M&A support to add key capabilities they need to drive growth. Specifically, this partnership brought best-in-class capabilities in back-office operations and institutional and independent distribution, complementing Saybrus Partners’ wholesaling and sales support model.

    The success of AmeriLife’s affiliate partners is also noteworthy. Four of its affiliate partners were recognized on the 2025 Inc. 5000 list of the fastest-growing private companies in America, including Florida Financial Advisors, Hoffman Financial Group, Brookstone Capital Management, and Pinnacle Financial Services. This recognition underscores the exceptional growth and innovative spirit of these companies, which are integral to AmeriLife’s mission.

    Companies on the Inc. Power Partner list received top marks from clients for being instrumental in helping leadership navigate the dynamic world of startups. These B2B partners support entrepreneurs across various business functions, including hiring, compliance, infrastructure development, cloud migration, fundraising, and more, allowing founders to focus on their core missions.

    “The entrepreneurial journey and community are core to Inc.’s mission, and it’s a true honor to celebrate this year’s Inc. Power Partners — the companies dedicated to helping small businesses and entrepreneurs,” says Bonny Ghosh, editorial director at Inc. “Whether they’re coordinating complex marketing campaigns or reliably supporting the day-to-day infrastructure of growing companies, these honorees aren’t simply B2B providers — they are true partners in helping businesses grow and succeed.”

    For more information or to view the complete list of honorees, visit Inc.com/Power-Partner-Awards.

    ###

    About AmeriLife

    AmeriLife’s strength lies in its mission: to provide insurance and retirement solutions that help people live longer, healthier lives. AmeriLife develops, markets, and distributes life and health insurance, annuities, and retirement planning solutions to enhance the lives of pre-retirees and retirees across the United States. For over 50 years, AmeriLife has partnered with top insurance carriers to provide value and quality to customers through a national distribution network of over 300,000 agents, financial professionals, and more than 160 marketing organizations and insurance agencies. For more information, visit AmeriLife.com and follow AmeriLife on Facebook and LinkedIn.

    About Inc.

    Inc. is the leading media brand and playbook for entrepreneurs and business leaders shaping our future. Through journalism, Inc. aims to inform, educate, and elevate the profile of its community: the risk-takers, the innovators, and the ultra-driven go-getters who are creating the future of business. Inc. is published by Manseto Ventures, along with fellow leading business publication Fast Company. For more information, visit www.inc.com.

    Contacts:

    Media

    Jeff Maldonado
    AmeriLife
    media@amerilife.com

    Partnership Inquiries

    Alex Hyer
    AmeriLife
    corporatedevelopment@amerilife.com

    .

    SOURCE: AmeriLife

    Related Images

    View the original press release on ACCESS Newswire

  • QorusDocs Named Best Proposal Management Software by Info-Tech SoftwareReviews and LegalTech Breakthrough Awards

    QorusDocs Named Best Proposal Management Software by Info-Tech SoftwareReviews and LegalTech Breakthrough Awards

    SEATTLE, WA / ACCESS Newswire / November 13, 2025 / QorusDocs, a leader in AI-powered value and proposal management software, has been recognized as the #1 proposal management solution by Info-Tech Research Group’s SoftwareReviews and awarded Proposal Management Software of the Year by the LegalTech Breakthrough Awards.

    “Our priority at QorusDocs is to streamline complex proposal and RFP processes for business development teams in professional services,” said Ray Meiring, CEO of QorusDocs. “These recognitions reflect our customers’ success-higher productivity, more consistency, and more time invested in client relationships and growth.”

    QorusDocs’ recognition as the top proposal management platform comes at a pivotal time as professional services organizations seek proven ways to harness AI, prove value to clients and stay ahead in a rapidly evolving landscape. According to the Thomson Reuters 2025 Generative AI in Professional Services Report, 95% of people in professional services believe AI will be central to their organization’s workflow within the next five years.

    Info-Tech SoftwareReviews: Top Proposal Management Software

    In SoftwareReviews’ Proposal Management Data Quadrant, QorusDocs ranks highest for product features and satisfaction as well as vendor experience and capabilities. The Info-Tech Buyer Experience Report (BXR), published in October 2025, highlights QorusDocs’ exceptional scores for product performance and customer relationships.

    According to a survey of QorusDocs users:

    • 100% say QorusDocs is critical to their success

    • 100% say it increases productivity

    • 100% plan to renew with QorusDocs

    • 96% love using QorusDocs

    • 93% would recommend QorusDocs

    • 81% believe the value outweighs the cost

    LegalTech Breakthrough Awards: Proposal Management Software of the Year

    LegalTech Breakthrough Awards, an independent market intelligence organization that evaluates and recognizes standout legal technology companies, products and services around the globe, selected QorusDocs as the Proposal Management Software of the Year.

    QorusDocs enables dozens of Am Law 200 and Global 200 Law Firms to automate pitches, proposals and RFP responses, boosting productivity by up to 60% and reducing formatting time by 50%. Capabilities include auto-generating first drafts, centralizing attorney bios, case studies, and credentials, and ensuring firm branding consistency.

    QorusDocs integrates with core law firm platforms, including Litera, Intapp Deal Cloud and Microsoft 365, to help firms produce winning proposals. The Pursuits feature helps law firms with managing collaboration and automation of the pitch process. Built on the Microsoft Azure OpenAI Service, QorusDocs addresses data security, compliance and privacy for law firms’ private content libraries, past RFPs, proposals, and internal documents.

    “Many large firms handle over 500 pitches per year, translating into thousands of non-billable hours devoted to repetitive, manual tasks,” said Bryan Vaughn, managing director of LegalTech Breakthrough. “Through its advanced AI-driven automation, seamless integration, and focus on the needs of legal teams, QorusDocs modernizes the proposal process, allowing legal professionals to reduce errors, increase efficiency and productivity, maintain brand consistency and win more business. We’re so pleased to recognize QorusDocs with ‘Proposal Management Software of the Year!’”

    Continued Product Innovation: Introducing QorusDocs Value Management and New Agentic Features to Drive Further Automation

    After acquiring AI-powered customer value management software Shark Finesse earlier this year, QorusDocs introduced Value Management, a collaborative solution for building out value assessments that helps revenue teams articulate and quantify business cases in their proposals, in October. Unlike traditional Excel-based approaches, QorusDocs Value Management drives standardized data-driven value models across the organization, ensuring consistency, accuracy and trust in the numbers. Firms and customers can collaborate and build business cases together, increasing engagement and credibility. 

    Additionally, at an October 28 customer event, QorusDocs previewed new AI agents and features coming to the platform in 2026 that will draw on deep industry expertise to help revenue teams draft, personalize and refine critical sales documents even faster. Users will be able to ask an AI agent to perform repeatable or complex tasks, such as finding content, researching information and creating documents.

    Over 25,000 people globally use QorusDocs, including dozens of Am Law 200 and Global 200 law firms. To learn more, visit www.qorusdocs.com.

    About QorusDocs

    QorusDocs is a Bellevue, WA-based leader in AI-powered Value and Proposal Management software, helping organizations prove ROI and win more business. The platform unites value management with proposal automation, enabling teams to build intelligent business cases and create personalized, data-driven pitches, presentations, proposals, and RFP responses. QorusDocs empowers business development, sales, marketing, and proposal teams to collaborate seamlessly, demonstrate measurable impact, and accelerate decisions.

    For more information, visit qorusdocs.com or follow us on LinkedIn.

    PR Contact

    Anna Rice
    anna.rice@alpinemarketingcomms.com

    SOURCE: QorusDocs

    View the original press release on ACCESS Newswire

  • Xenetic Biosciences, Inc. Reports Third Quarter 2025 Financial Results

    Xenetic Biosciences, Inc. Reports Third Quarter 2025 Financial Results

    Continued execution on collaborations and exploratory investigator-initiated studies with institutional partners

    Secured net proceeds of approximately $3.9 million from October 2025 offering

    FRAMINGHAM, MA / ACCESS Newswire / November 13, 2025 / Xenetic Biosciences, Inc. (NASDAQ:XBIO) (“Xenetic” or the “Company”), a biopharmaceutical company focused on advancing innovative immuno-oncology technologies addressing difficult to treat cancers, today reported its financial results for the third quarter 2025.

    “We are steadily building the foundation for potentially transformative progress in the oncology treatment paradigm as we advance our systemic DNase I program in combination with established cancer therapies,” commented James Parslow, Interim Chief Executive Officer and Chief Financial Officer of Xenetic. “The partnerships we’ve formed continue to generate critical data that we believe will help us guide our development and regulatory strategies to fully realize the promise of our DNase technology. The underwritten public offering we completed in October 2025 extends our cash runway and provides us additional capital to continue to invest in pre-clinical efforts and exploratory studies and advance our technology toward an IND submission and Phase 1 initiation.”

    Xenetic continues to advance its DNase-based technology towards Phase 1 clinical development for the treatment of pancreatic carcinoma and other locally advanced or metastatic solid tumors. Preclinical proof-of-concept studies combining DNase I with chemotherapy, immunotherapies, and CAR-T therapy in hematological and solid tumor and metastatic cancer models have been completed. Building on proof-of-concept success, the program has now advanced to mechanism-of-action and translational studies in preparation for a Phase 1 clinical trial.

    Additionally, as previously announced in December 2024, Xenetic entered into a Clinical Trial Services Agreement with PeriNess, under which PeriNess will lead in the regulatory approval, operational execution and management of potential exploratory, investigator initiated studies of recombinant DNase as an adjunctive treatment in patients with pancreatic carcinoma and other locally advanced or metastatic solid tumors receiving chemotherapy and immunotherapy in Israeli medical centers.

    Summary of Financial Results for Third Quarter 2025
    Net loss for the quarter ended September 30, 2025 was approximately $0.5 million. Research & development expenses for the three months ended September 30, 2025 increased by approximately $0.4 million, or 105.6%, to approximately $0.8 million from $0.4 million in the comparable quarter in 2024 primarily due to increased manufacturing development efforts and pre-clinical research as well as increased consulting costs. General and administrative expenses for the three months ended September 30, 2025 increased by approximately $0.1 million, or 9.3%, to approximately $0.8 million from approximately $0.7 million in the comparable quarter in 2024 primarily due to increased legal costs in connection with the Company’s strategic review process.

    Revenue for the three months ended September 30, 2025 increased by approximately $0.4 million, or 67.2%, to approximately $1.0 million from approximately $0.6 million for the three months ended September 30, 2024. This increase represented an increase in royalty revenue related to Xenetic’s sublicense agreement with Takeda Pharmaceuticals Co. Ltd. as compared to the same period in 2024 primarily due to royalties recognized from certain countries during the third quarter of 2025 compared to the same period in 2024.

    The Company ended the quarter with approximately $4.1 million cash. Subsequent to quarter end, the Company closed an underwritten offering for net proceeds of approximately $3.9 million.

    About Xenetic Biosciences
    Xenetic Biosciences, Inc. is a biopharmaceutical company focused on advancing innovative immuno-oncology technologies addressing difficult to treat cancers. The Company’s DNase platform is designed to improve outcomes of existing treatments, including immunotherapies, by targeting neutrophil extracellular traps (NETs), which are involved in cancer progression. Xenetic is currently focused on advancing its systemic DNase program into the clinic as an adjunctive therapy for pancreatic carcinoma and locally advanced or metastatic solid tumors.

    For more information, please visit the Company’s website at www.xeneticbio.com and connect on X, LinkedIn, and Facebook.

    Forward-Looking Statements
    This press release contains forward-looking statements that we intend to be subject to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release other than statements of historical facts may constitute forward-looking statements within the meaning of the federal securities laws. These statements can be identified by words such as “expects,” “plans,” “projects,” “will,” “may,” “anticipates,” “believes,” “should,” “intends,” “estimates,” “remain,” “focus”, “confidence in”, “potential”, “continue”, “advance”, “fully realize”, “promise”, and other words of similar meaning, including, but not limited to, all statements regarding expectations for our DNase-base oncology platform, including statements regarding: potentially transformative progress in the oncology treatment paradigm as we advance our systemic DNase I program in combination with established cancer therapies; our partnerships continuing to generate critical data that we believe will help us guide our development and regulatory strategies to fully realize the promise of our DNase technology; plans to continue to invest in pre-clinical efforts and exploratory studies and advance our technology toward an IND submission and Phase 1 initiation; plans to advance our DNase-based oncology technology towards Phase 1 clinical development for the treatment of pancreatic carcinoma and other locally advanced or metastatic solid tumors; plans to build on proof-of-concept success; expectations regarding mechanism-of-action and translational studies in preparation for a Phase 1 clinical trial; expectations regarding our partnership with PeriNess and anticipated outcomes under the clinical services agreement; our focus on advancing innovative immune-oncology technologies addressing difficult to treat cancers; expectations regarding the DNase platform improving outcomes of existing treatments, including immunotherapies, by targeting NETs, which are involved in cancer progression; and our focus on advancing our systemic DNase program into the clinic as an adjunctive therapy for pancreatic carcinoma and locally advanced or metastatic solid tumors. Any forward-looking statements contained herein are based on current expectations and are subject to a number of risks and uncertainties. Many factors could cause our actual activities, performance, achievements, or results to differ materially from the activities and results anticipated in forward-looking statements. Important factors that could cause actual activities, performance, achievements, or results to differ materially from such plans, estimates or expectations include, among others, (1) unexpected costs, charges or expenses resulting from our manufacturing and collaboration agreements; (2) unexpected costs, charges or expenses resulting from the licensing of the DNase platform; (3) uncertainty of the expected financial performance of the Company following the licensing of the DNase platform; (4) failure to realize the anticipated potential of the DNase or PolyXen technologies; (5) the ability of the Company to obtain funding and implement its business strategy; (6) risks and uncertainties as to the outcome and timing of the strategic review process being conducted by the Board and a special independent committee thereof, including the possibility that the Board may decide not to undertake a strategic alternative following the evaluation process, the Company’s inability to consummate any proposed strategic alternative resulting from the review due to, among other things, market, regulatory and other factors, the potential for disruption to our business resulting from the review process, and potential adverse effects on the Company’s stock price from the announcement, suspension or consummation of the evaluation process and the results thereof, as well as risks and uncertainties related to the potential impacts of consummation of a strategic transaction on the Company’s current business operations, anticipated business strategy and product development plans; and (7) other risk factors as detailed from time to time in the Company’s reports filed with the SEC, including its annual report on Form 10-K, periodic quarterly reports on Form 10-Q, current reports on Form 8-K and other documents filed with the SEC. The foregoing list of important factors is not exclusive. In addition, forward-looking statements may also be adversely affected by general market factors, general economic and business conditions, including potential adverse effects of public health issues, and geopolitical events, such as the conflicts in Ukraine and in the Middle East, on economic activity, competitive product development, product availability, federal and state regulations and legislation, the regulatory process for new product candidates and indications, manufacturing issues that may arise, patent positions, litigation, and shareholder activism, among other factors. The forward-looking statements contained in this press release speak only as of the date the statements were made, and the Company does not undertake any obligation to update forward-looking statements, except as required by law.

    CONTACT:
    JTC Team, LLC
    Jenene Thomas
    (908) 824-0775
    xbio@jtcir.com

    SOURCE: Xenetic Biosciences, Inc.

    View the original press release on ACCESS Newswire

  • FAEMA Launches FAEMINA in the United States: The Italian Espresso Experience, Redefined for Home and Small Spaces

    FAEMA Launches FAEMINA in the United States: The Italian Espresso Experience, Redefined for Home and Small Spaces

    FAEMA, the legendary Italian espresso brand from the Cimbali Group, proudly announces the U.S. debut of FAEMINA, its first high-end espresso machine designed specifically for the home, office, and small business market. FAEMINA unites timeless Italian craftsmanship, advanced technology, and contemporary design to make barista-quality coffee accessible anywhere.

    NEW YORK CITY, NEW YORK / ACCESS Newswire / November 13, 2025 / A Machine Born from Italian Excellence

    Faemina-Professional-Espresso-Machine
    Faemina-Professional-Espresso-Machine
    Faemina combines professional performance with Italian design

    Designed by ItalDesign, FAEMINA embodies Italian design values: elegance, functionality, and precision craftsmanship. Its minimalist aesthetic complements modern interiors while housing the same performance DNA that defines FAEMA’s professional machines. Every detail is engineered for ease of use and consistency, ensuring perfect extractions cup after cup.

    Professional Performance, Simplified for Everyday Use

    Hand-built in Italy, FAEMINA brings professional-grade technology to a compact, plug-and-play format. Key features include:

    • Dual Boiler System for simultaneous brewing and steaming.

    • Smart Temperature Control for pre-infusion and stable extraction.

    • Wide drink Range: from espresso to filter coffee and tea infusions.

    • Optional AutoSteam function forperfect milk at the touch of a button.

    • Internal Water Tank delivers stability and convenience.

    This combination allows anyone, from coffee lovers to first-time users, to enjoy café-quality espresso and milk-based beverages without technical expertise.

    Beyond Home: The New Standard for Small Businesses

    FAEMINA is ideal not only for the home but also for boutiques, concept stores, hotel lounges, and small offices seeking a premium coffee experience. Compact yet powerful, it turns coffee preparation into a visual and sensory ritual, transforming any space into a corner of Italian hospitality.

    Accessible Luxury: How to Buy

    FAEMINA is now available in the United States through:

    A range of accessories and finishes allows customers to personalize their setup, ensuring FAEMINA fits seamlessly into every environment.

    Why Choose FAEMINA:

    • Authentic Italian Heritage: From the makers of the iconic FAEMA E61, a milestone in espresso technology.

    • Designed for Modern Living: Compact, quiet, and built to perform.

    • Sustainable Craftsmanship: High-quality materials designed to last.

    • Versatility: Ideal for espresso, cappuccino, latte art, and specialty brews. With dedicated filter coffee and infusion tea functions, it lets you set the perfect temperature for every drink.

    FAEMINA represents the evolution of espresso, combining form, function, and emotion to bring the authentic Italian café experience into everyday life.

    Availability and Contact

    Discover FAEMINA today at www.faema.com or on Amazon.com.

    About FAEMA

    Founded in Milan in 1945, FAEMA is part of Cimbali Group, one of the world’s leading manufacturers of professional coffee machines. The brand defined the history of espresso through innovation, design, and Italian craftsmanship. FAEMA introduced the legendary E61, the first machine to use a volumetric pump to deliver consistent nine-bar pressure, revolutionizing espresso preparation. Today, FAEMA continues to merge technology and tradition to create machines that embody the art of Italian coffee culture, from professional cafés to homes worldwide.

    Instagram: @faema_official | @faemina_official

    Contact Information

    Faema Marketing
    Marketing Team
    marketing@cimbaligroup.com

    .

    SOURCE: FAEMA

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    View the original press release on ACCESS Newswire

  • Franchise Builders Announces Strategic Partnership

    Franchise Titan Janice Charles Joins Team to Launch Next-Gen Franchising Platform

    CHATTANOOGA, TN / ACCESS Newswire / November 13, 2025 / Franchise Builders™, the high-velocity engine dedicated to scaling franchise systems, today announced a strategic partnership with Janice Charles, one of the most respected voices in the franchising industry. With a network of hundreds of franchisors representing more than 15,000 locations, Ms. Charles brings unparalleled influence, insight and reach – enabling Franchise Builders™ to accelerate its mission of transforming the way franchises form, scale and transact.

    Franchise Builders™’ vision: Using AI, automation and ecosystem infrastructure, Franchise Builders™ provides the solution for emerging and established franchisors to launch, manage and grow at scale. By formalizing this partnership with Janice Charles, Franchise Builders™ is taking a major leap towards its goal to become the “MLS of Franchising”: the go-to platform where franchise systems are listed, matched, benchmarked and scaled. “Partnering with Janice marks a turning point in our mission,” said Nash Bowen, Founder of Kronos Capital™, the private equity firm backing Franchise Builders™. “Her credibility across the franchising ecosystem gives us access to early brand adoption, system-wide data and operational insight – positioning us to be the backbone of the next generation of franchise growth.”

    Partnership with Janice Charles: With 40+ years of franchise experience (including time as a franchisee, franchise-system operator, and franchise consultant), Janice Charles has developed deep relationships across the industry, worked with top consumer brands and guided hundreds of franchisor systems through growth phases. Her appointment as an equity partner ensures Franchise Builders™ not only builds powerful technology – but builds it in lock-step with the realities of franchisor needs, unit economics, brand consistency and operational scalability. “I’m excited to join forces with Franchise Builders™,” said Janice Charles. “Franchise systems have long needed a unified, technology-forward platform that handles discovery, performance benchmarking, system optimization and growth. Together we can give franchisors the tools and visibility they deserve – and unlock value for the entire network.”

    Strategic partnership highlights:

    • Janice Charles will leverage her network of franchisors to integrate the Franchise Builders™ platform, enable pilot programs and accelerate adoption across thousands of units.

    • Franchise Builders™ will embed Janice’s thought-leadership, best practices and franchise operator feedback into its platform road map – aligning product development with real-world brand growth levers.

    • Together they will co-launch features that bring transparency, benchmarking and discovery to the franchise space – enabling brands, advisors and investors to access a centralized, efficient marketplace for franchise models, growth stages, capital raising and unit performance.

    About Franchise Builders™

    Franchise Builders™ is a franchise platform designed to accelerate unit expansion through AI-driven tooling, performance analytics, efficient infrastructure and monetization features, allowing franchisors to streamline development, monitor performance, optimize royalties, and scale faster.

    About Janice Charles

    Janice Charles is a leading franchise industry consultant and operator with more than four decades of experience as a franchisee, franchisor advisor and system growth strategist. She is widely recognized for her deep domain expertise, brand relationships, integrity in franchising, and success scaling leading franchise networks.

    Contact Information

    Luke DeFrino
    Marketing Manager
    luke@kronoscapital.us
    (860) 388-7488

    .

    SOURCE: Kronos Media

    View the original press release on ACCESS Newswire

  • Femm Parlour Opens in New York City, Turning Intimate-Health Conversations Into Care

    New York, NY November 13, 2025 –(PR.com)– FEMM Parlour (FEMM) has opened in New York City to turn dismissed intimate-health concerns into clear plans of care, through cutting-edge technology.

    Many women facing intimate health challenges are often dismissed by providers who attribute these issues to gender, FEMM refuses to accept that these concerns are just a part of being women. Through FDA-approved treatments common issues are effectively addresses, with no pain, stigma or downtime.

    At FEMM, empowerment is not a slogan, it’s the standard of care. The process starts with a private consultation where patients are heard, without euphemisms. From that conversation, each woman receives a personalized plan explained in plain language, alongside built-in follow-ups so progress is tracked and care evolves. The goal is simple: give women answers they can trust and steps they can take now, not someday.

    “We’re not just a clinic; we’re a movement,” said Gina Cappelli. “We’re building a space where intimate health is approached with dignity and clarity, ensuring that every woman can confidently address her unique needs. We take concerns that have been minimized or dismissed and turn them into a plan of action.”

    That plan of action is deliberately designed around a woman’s life, not the other way around. Care is delivered in straightforward terms, and the experience emphasizes comfort throughout. Non-surgical options are selected for practicality and accessibility, with no pain and no downtime, so women do not have to choose between addressing their health and keeping their day intact.

    “Awareness matters but women are ready for answers,” said Cindy Barshop. “Our job is to listen, to lay out options without pressure, and to guide her through a plan that feels comfortable and credible. The measure of success is not a good conversation; it’s a woman walking out with next steps she believes in.”

    FEMM’s approach extends beyond the appointment. When appropriate, clinicians integrate clinically informed intimacy tools to support at-home continuity between visits, keeping momentum steady without turning care into a performance. Every touchpoint reinforces the same idea: progress should be visible, supported, and personal.

    “This is the clinic we wished existed,” added Cappelli. “It’s precise and empathetic. It centers a woman’s goals and builds a path that meets her where she is. No one should have to navigate intimate health alone.”

    FEMM was built for the woman who is done waiting, who wants clarity instead of guesswork, who wants to feel at home in her body at every stage of life. By replacing stigma with straight talk and inertia with step-by-step care FEMM turns intention into outcome, one private consult, one personalized plan, and one documented follow-up at a time.

    Media note: Editorial walk-throughs and clinician interviews are available on request.

    About FEMM Parlour

    FEMM Parlour is a New York City destination for women’s intimate wellness. Cindy Barshop has joined forces with Gina Cappelli and Maria Trusa to offer discreet consultations, physician guided non-surgical treatments, and a curated selection of clinically informed intimacy products. The clinic’s focus is practical, dignified solutions that help women feel at home in their bodies at every stage of life.

    Website: www.femmparlour.com
    Instagram: @femmparlour
    Media Contact: Eleonora Mercier | ellie@marketlycollective.com | (973) 900-1708

    Contact Information:
    Femm Parlour
    Eleonora Mercier
    +1 9739001708
    Contact via Email

    Read the full story here: https://www.pr.com/press-release/953134

    Press Release Distributed by PR.com

  • CreditBlockchain Launches Cloud Mining Platform for BTC, ETH, and BNB Holders

    Denver, CO November 12, 2025 –(PR.com)– CreditBlockchain has announced the launch of an AI-powered cloud mining platform that supports BTC, XRP, and SOL mining. The platform features automated hashrate allocation, publicly verifiable withdrawals, and access via mobile devices or web browsers.

    Platform Highlights:

    – Intelligent scheduling: The system analyzes factors such as mining difficulty, energy use, and network conditions to automatically allocate computing power across multiple mining pools and asset types.

    – Automated settlement: The platform calculates user account balances daily based on mining performance. Users may withdraw balances to a personal wallet or maintain them within the platform for continued participation.

    – Mobile and web access: The platform’s interface is designed for both mobile and web use, allowing users to view computing allocations, mining status, and account information.

    – Transparency: Each mining plan displays its pricing, term, and cost details. Withdrawal transactions can be verified on a public blockchain.

    – Standardized operation: Parameters and rules related to settlement and withdrawal are publicly available to ensure operational consistency.

    How to Use:

    1. Registration: Create an account through the CreditBlockchain website or app.

    2. Top-up: Add supported digital assets (BTC, XRP, ETH, or stablecoins) to the account.

    3. Plan Selection: Choose from available computing power plans, which include pricing and term information.

    4. Account Management: Settlements are applied to user balances daily and can be withdrawn to a linked on-chain wallet.

    Safety and Infrastructure:

    – Security: TLS 1.3 transport encryption, AES-256 data protection, login verification, and DDoS protection are implemented.

    – Operations: Data centers use N+1 power and cooling architecture with 24/7 monitoring and multi-regional disaster recovery to support continuous operation.

    – Transparency: Fees, parameters, and withdrawal records can be viewed and verified on-chain.

    A CreditBlockchain spokesperson stated:
    “Our goal is to provide a transparent and stable digital mining platform supported by verifiable on-chain data and standardized operational practices.”

    Company Vision
    CreditBlockchain aims to promote sustainable practices in digital computing and support technological advancement with operational transparency and environmental responsibility.

    Media Contact Information
    CreditBlockchain
    Official Website: creditblockchain.com
    Email: info@creditblockchain.com

    Contact Information:
    Credit Blockchain
    +447723578944
    Contact via Email
    creditblockchain.com

    Read the full story here: https://www.pr.com/press-release/953085

    Press Release Distributed by PR.com

  • Eminent Spine’s 3D Printed Titanium Posterior SI System Receives FDA 510(k) Clearance

    Plano, TX November 12, 2025 –(PR.com)– Eminent Spine, a leader in spinal implant innovation, proudly announces that its revolutionary 3D Printed Titanium Posterior SI System has received FDA 510(k) clearance as of October 7, 2025.

    Innovative Design & Superior Engineering
    The 3D Printed Titanium Posterior in-line transfixing implant was designed with both surgeon precision and patient outcomes in mind. Key features include:

    · SI Compression and Transfixation of SI joint
    · Aggressive Lordotic teeth to resist migration
    · Large central opening for maximum bone graft material
    · Tapered nose and rounded edges allows for ease of insertion

    Implant profiles are 25mm x 14mm x 8mm Lordotic implant.
    Screw options are offered in 3.5 or 3.75mm + lengths from 10-18mm.
    Implants have built-in locking tabs.

    Eminent Spine’s commitment to benchmark biomechanical testing and extensive cadaver biomechanical testing resulting in an anatomic 3D posterior transfixing implant. With the approval of the posterior approach and lateral, superior lateral and S2-AI approaches, Eminent Spine can now offer the patient and the surgeon a comprehensive system for SI joint fusion procedures. The multiple FDA approved approaches ensures safety, reliability and superior clinical outcomes.

    “With the 3D posterior titanium inline transfixing FDA 510(k) Eminent Spine is now able to offer a comprehensive system treating SI joint dysfunction,” says Dr. Stephen Courtney, Founder and CEO of Eminent Spine.

    This is Eminent Spine’s 9th FDA 510(k) clearance letter since 2020.

    About Eminent Spine
    Founded with a vision to redefine spinal solutions, Eminent Spine specializes in developing high-performance, surgeon-driven spinal implants. With a focus on biomechanics, surgical efficiency, and patient recovery, Eminent Spine remains at the forefront of orthopedic and spinal innovation.

    For more information about the 3D Printed Titanium Posterior SI System or to schedule a demonstration, please visit www.eminentspine.com.

    Contact Information:
    Eminent Spine
    Eminent Spine
    972-499-3593
    Contact via Email
    www.eminentspine.com

    Read the full story here: https://www.pr.com/press-release/953606

    Press Release Distributed by PR.com