STOCK TITAN

Creative Medical Technology Holdings, Inc. Expands Ultrasome™ Intellectual Property Portfolio with New U.S. Provisional Patent Filing

Creative Medical strengthens Ultrasome’s patent position while highlighting prior osteoarthritis pilot data and ongoing platform expansion efforts.

(Very Positive)
Tags

Creative Medical Technology Holdings (CELZ) filed a new U.S. provisional patent application to broaden protection of its Ultrasome™ cell-free regenerative medicine platform.

The filing seeks coverage for product composition, biological potency, manufacturing and quality-control methods, stability, delivery approaches and therapeutic applications, including musculoskeletal and cartilage disorders. It builds on an earlier pilot knee osteoarthritis study in which about 93% of patients showed clinically meaningful mobility and pain improvements with no serious adverse events. The application establishes a U.S. priority date but has not yet been examined, and future patent scope or issuance is not assured.

Loading...
Loading translation...

Positive

  • New Ultrasome™ provisional patent filing broadens protection across composition, potency, manufacturing and applications
  • Prior knee osteoarthritis pilot reported ~93% of participants with clinically meaningful mobility and pain improvements
  • No serious adverse events were reported in the previously announced Ultrasome knee osteoarthritis pilot study
  • Single GMP-based cellular source and FDA Drug Master File may support scalability and product consistency
  • Provisional filing establishes an initial U.S. priority date for Ultrasome-related intellectual property

Negative

  • Provisional patent has not been examined and there is no assurance of future patent claim scope or issuance
  • Additional musculoskeletal and cartilage applications are in R&D and are not evidence of clinical efficacy or regulatory approval
  • FDA Drug Master File for the platform does not constitute FDA approval, clearance or authorization of a therapeutic product

News Explained

The filing adds no demonstrated clinical or regulatory status: the company says additional Ultrasome applications remain in research and development, while the provisional application has not been examined by the U.S. Patent and Trademark Office.

Market Context

Before publication, CELZ had recorded -7.12% over 24 hours on 0.2x average volume; this provisional ...
Analysis

Before publication, CELZ had recorded -7.12% over 24 hours on 0.2x average volume; this provisional filing entered a weak, low-volume pre-headline session while the application remained unexamined.

Key Figures

Clinically meaningful improvement: 93%
Clinically meaningful improvement
93%
April 2026 knee osteoarthritis pilot participants

Historical Context

1 past event · Latest: Aug 06
1 event
  1. Aug 06

    Patent allowance

    24h Move
    +72.0%

    USPTO notice of allowance expanded exosome-based immunotherapy protection across diabetes platforms

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

Key Terms

provisional patent application, functional potency, extracellular-vesicle, good manufacturing practice, +1 more
5 terms
provisional patent application regulatory
"The newly filed provisional patent application seeks intellectual property protection"
A provisional patent application is a lightweight, temporary filing that records an inventor’s idea and sets an official filing date without starting the full patent review process. Think of it as placing a hold on an idea while you prepare the complete paperwork; it doesn’t grant a patent but can preserve the right to seek one later. For investors, it signals a company is protecting potential intellectual property, which can affect future competitive advantage and valuation, but it is not a guarantee of patent protection.
functional potency technical
"including proprietary product composition, biological potency, manufacturing"
A laboratory measure of how well a drug, biologic, or therapeutic product produces its intended biological effect in a functional test, usually reported as the activity per unit of material. It matters to investors because it helps show whether a product consistently does what it is supposed to do, affects dosing and manufacturing specifications, and is often used by regulators to judge quality and comparability—think of it like testing how many lightbulbs of the same model actually reach the same brightness.
extracellular-vesicle medical
"the field of extracellular-vesicle and secretome-based therapeutics"
Small, membrane-bound particles that cells naturally release into bodily fluids, carrying proteins, lipids, and nucleic acids that reflect the cell’s state. Like biological “messages in a bottle,” extracellular vesicles can be measured or engineered for diagnostics, drug delivery, and therapeutic development, so they matter to investors because they underpin product pipelines, manufacturing challenges, and regulatory considerations in biotechnology and diagnostics.
good manufacturing practice regulatory
"derived from an independently validated Good Manufacturing Practice master cell bank"
Good manufacturing practice (GMP) are the rules and routines companies must follow to make products consistently safe and effective, covering everything from equipment and cleanliness to staff training and recordkeeping. For investors, GMP compliance signals lower risk of product failures, regulatory fines, production stoppages or costly recalls—like a reliable recipe and tidy kitchen that help ensure every batch turns out the same and customers stay satisfied.
drug master file regulatory
"within a U.S. Food and Drug Administration Drug Master File"
A drug master file (DMF) is a confidential technical dossier submitted to regulators that describes the detailed chemistry, manufacturing and quality controls for an active drug ingredient or key component. Think of it as a supplier’s locked recipe and factory blueprint that regulators can inspect without the buyer revealing trade secrets. For investors, a DMF matters because it supports product approvals, protects supply-chain know‑how, and can speed regulatory review or signal manufacturing readiness.

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

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

New Filing Seeks Broad Protection Around Creative Medical’s Cell-Free Regenerative Platform, Including Product Composition, Functional Potency, Manufacturing Controls and Additional Therapeutic Applications

PHOENIX, Sept. 17, 2026 (GLOBE NEWSWIRE) -- Creative Medical Technology Holdings, Inc. (NASDAQ: CELZ) ("Creative Medical" or the "Company"), a clinical-stage biotechnology company advancing regenerative medicine solutions, today announced the filing of a new U.S. provisional patent application designed to expand intellectual property protection surrounding Ultrasome™, the Company’s proprietary cell-free regenerative medicine platform.

The newly filed application builds upon Creative Medical’s existing regenerative medicine intellectual property and seeks protection across multiple aspects of the Ultrasome platform, including proprietary product composition, biological potency, manufacturing and quality-control methodologies, stability characteristics, delivery approaches and therapeutic applications.

The filing is intended to strengthen the Company’s long-term intellectual property position as Creative Medical advances Ultrasome beyond its initial osteoarthritis program and evaluates the platform’s potential across additional areas of regenerative medicine.

“As our understanding of the Ultrasome platform continues to advance, we believe it is important to protect not only its therapeutic applications, but also the underlying product characteristics, biological activity and manufacturing framework that distinguish the platform,” said Timothy Warbington, President and Chief Executive Officer of Creative Medical Technology Holdings. “This filing represents another step in building a broad intellectual property estate around what we believe can become a highly scalable cell-free regenerative medicine platform.”

Building Intellectual Property Around Product Function, Not Simply Particle Identity

Creative Medical’s development strategy for Ultrasome incorporates both physical product characterization and biologically relevant functional testing designed to evaluate activity associated with tissue protection and regenerative signaling.

The newly filed provisional patent application seeks intellectual property protection around multiple aspects of this approach, including methods intended to characterize the biological activity and consistency of manufactured product.

Management believes that integrating product composition, functional potency and manufacturing control may provide important differentiation as the field of extracellular-vesicle and secretome-based therapeutics continues to evolve.

The patent application also includes intellectual property directed toward methods for evaluating changes in product biological activity that may not be reflected by particle measurements alone.

“A central component of our development strategy is establishing reproducible biological activity across manufactured product,” Warbington added. “We believe that connecting manufacturing, product characterization and functional performance is important both scientifically and strategically as we advance this platform.”

Builds on Previously Announced Ultrasome™ Knee Osteoarthritis Program

The new patent filing follows Creative Medical’s previously announced pilot study evaluating Ultrasome in patients with knee osteoarthritis.

As announced in April 2026, the study reported that approximately 93% of participants demonstrated clinically meaningful improvements in mobility and pain, and no serious adverse events were reported.

The Company continues to view osteoarthritis as an important initial application for Ultrasome while exploring the broader potential of the platform across regenerative medicine.

The new provisional filing includes intellectual property intended to preserve development flexibility for musculoskeletal and cartilage disorders as well as selected clinical applications. These additional applications remain in various stages of research and development and should not be interpreted as evidence of clinical efficacy or regulatory approval in those indications.

Extending a GMP-Based Regenerative Medicine Platform

Ultrasome is being developed from Creative Medical’s proprietary Olastrocel™ regenerative medicine platform.

The underlying cellular source is derived from an independently validated Good Manufacturing Practice master cell bank, with manufacturing and quality information maintained within a U.S. Food and Drug Administration Drug Master File.

A Drug Master File is a confidential regulatory submission containing manufacturing and quality information and does not itself constitute FDA approval, clearance or authorization of a therapeutic product.

Creative Medical believes the ability to leverage a controlled cellular starting material across both cell-based and cell-free programs may support future manufacturing scalability, product consistency and expansion of its regenerative medicine pipeline.

Expanding Creative Medical’s Intellectual Property Portfolio

The new application is part of Creative Medical’s strategy of building intellectual property protection around multiple layers of its regenerative medicine technologies, including:

  • proprietary cell-free compositions;
  • functional biological characteristics;
  • manufacturing and quality-control methodologies;
  • stability and product-release approaches;
  • targeted delivery methods; and
  • therapeutic applications across selected regenerative medicine indications.

As a provisional patent application, the filing establishes an initial U.S. priority date for the disclosed subject matter and provides the Company with the opportunity to pursue U.S. and international patent protection through subsequent filings.

The provisional application has not been examined by the U.S. Patent and Trademark Office, and there can be no assurance regarding the scope or issuance of any future patent claims.

Strategic Focus

Creative Medical intends to continue advancing its intellectual property portfolio in parallel with its clinical and translational development programs.

Management believes a combination of clinical development, proprietary manufacturing, functional product characterization and intellectual property protection may create multiple opportunities for future platform development, strategic collaboration and value creation.

“Our goal is to build durable value around the science,” Warbington concluded. “We believe the combination of our clinical-stage regenerative platform, expanding cell-free programs and growing intellectual property portfolio positions Creative Medical to pursue multiple high-value opportunities while maintaining disciplined development of our core programs.”

About Ultrasome™

Ultrasome™ is Creative Medical Technology Holdings’ proprietary cell-free regenerative medicine platform derived from the Company’s umbilical cord tissue technology. The platform is being developed to deliver biologically active regenerative signals through scalable, off-the-shelf formulations for potential use across selected degenerative and regenerative medicine applications.

Ultrasome’s initial clinical development has focused on osteoarthritis of the knee.

About Creative Medical Technology Holdings, Inc.

Creative Medical Technology Holdings, Inc. (NASDAQ: CELZ) is a biotechnology company advancing regenerative medicine therapies derived from adult and perinatal cell technologies. The Company’s programs span multiple areas of regenerative medicine and are designed to translate proprietary cellular and cell-free technologies into therapeutic opportunities for patients with significant unmet medical needs.

For more information, please visit www.creativemedicaltechnology.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of applicable federal securities laws, including statements regarding the potential scope and value of the Company’s intellectual property portfolio; the development, scalability, manufacturing, potential therapeutic applications and commercial potential of Ultrasome™; future patent prosecution and patent issuance; future clinical and translational development; potential strategic collaborations; and the Company’s plans to evaluate additional regenerative medicine indications. Forward-looking statements are based on current expectations and assumptions and involve risks and uncertainties that could cause actual results to differ materially from those expressed or implied. These risks include, among others, risks associated with patent prosecution and enforcement, clinical development, regulatory review, manufacturing, scientific validation, financing, market acceptance and other risks described in the Company’s filings with the Securities and Exchange Commission.

A provisional patent application is not examined by the USPTO and does not guarantee that a patent will issue or that any subsequently issued claims will provide commercially meaningful protection.

Creative Medical Technology Holdings, Inc. undertakes no obligation to update forward-looking statements except as required by applicable law.

Investor & Media Contacts

Creative Medical Technology Holdings, Inc.
IR@CreativeMedicalTechnology.com
www.creativemedicaltechnology.com

Investor Relations / The Equity Group Inc.
Devin Sullivan
devin.sullivan@theequitygroup.com Conor Rodriguez
conor.rodriguez@theequitygroup.com


FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What aspects of the Ultrasome™ platform does the new provisional patent filing seek to protect?

The new U.S. provisional patent application seeks protection for multiple Ultrasome™ elements, including proprietary product composition, biological potency, manufacturing and quality-control methodologies, stability characteristics, targeted delivery approaches and therapeutic applications, including musculoskeletal and cartilage disorders and selected additional regenerative medicine indications.

How does this filing relate to Creative Medical’s knee osteoarthritis program?

The filing follows a previously announced pilot study of Ultrasome™ in knee osteoarthritis in which approximately 93% of participants demonstrated clinically meaningful improvements in mobility and pain and no serious adverse events were reported. Osteoarthritis remains an initial application focus, while the new intellectual property is intended to preserve development flexibility for broader musculoskeletal and cartilage disorders.

What is the role of the GMP-based Olastrocel™ platform in Ultrasome™ development?

Ultrasome™ is being developed from the Olastrocel™ regenerative medicine platform, which uses an independently validated Good Manufacturing Practice master cell bank as the cellular source. Manufacturing and quality information are maintained within a U.S. Food and Drug Administration Drug Master File. The company believes this controlled starting material can support manufacturing scalability, product consistency and expansion across both cell-based and cell-free programs.

What does filing a provisional patent application accomplish for Creative Medical?

As a provisional patent application, the filing establishes an initial U.S. priority date for the disclosed Ultrasome™ subject matter and provides the opportunity to pursue U.S. and international patent protection through later filings. The provisional application itself has not been examined by the U.S. Patent and Trademark Office, and there is no guarantee as to the scope or issuance of any future patent claims.

How does Creative Medical describe its broader intellectual property strategy?

The company describes a strategy of building intellectual property around multiple layers of its regenerative technologies, encompassing proprietary cell-free compositions, functional biological characteristics, manufacturing and quality-control methods, stability and product-release approaches, targeted delivery methods and therapeutic applications across selected regenerative medicine indications, in parallel with clinical and translational development programs.

Keep reading