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Human Studies

SMS cells are being evaluated in human studies to assess their potential in treating diseases such as:

Researcher conducting human studies on SMS stem cells under a microscope to evaluate their potential in treating degenerative diseases.
Clinical research with SMS stem cells, highlighting their potential applications in treating degenerative diseases through human studies.
SMSbiotech investigates COPD therapies with stem cell nebulization, supported by clinical imaging and patient trials.

Respiratory diseases:

COPD

Bio-manufactured SMS cells are administered via nebulization, enabling direct delivery to the lungs. Their unique size and resilience characteristics make this method of cell delivery feasible and effective. A phase 1 clinical trial is currently enrolling 18 patients with mild to moderate COPD, organized into three ascending-dose cohorts.

The primary endpoint is safety and tolerability, while secondary and exploratory endpoints include early signs of efficacy, such as improvements in lung function, reduction in exacerbation frequency, and enhanced patient-reported outcomes.

Unlocking Cartilage Repair with SMS Cells

Chondrocyte Regeneration

Small Mobile Stem (SMS) cells have been tested for their effect on chondrocytes—the key cells responsible for producing and maintaining joint cartilage.

Binding of Small Mobile Stem (SMS) cells to chondrocytes triggers changes in the expression of thousands of genes, with the overall pattern strongly supporting cartilage repair and reduction or elimination of pain and inflammation.

Orthopedic specialist demonstrating human knee joint structure and cartilage using an anatomical model to explain SMS Biotech regenerative therapies.
Medical professional demonstrating knee joint anatomy with a model
Knee tendon and ligament anatomy explained by an orthopedic expert during a regenerative therapy consultation.
Knee tendon and ligament anatomy explained by an orthopedic expert during a regenerative therapy consultation.

Tendon and Ligament Regeneration

Small Mobile Stem (SMS) cells have been tested for their effect on Tenocytes, the key cells responsible for producing and maintaining tendons. Due to lack of vascularization Tendons and Ligaments are tissues that lack in their ability to repair and regenerate.

Binding Small Mobile Stem (SMS) cells to Tenocytes triggers changes in the expression of many genes in Tenocytes, with the overall pattern strongly supporting tissue repair. SMS cells can stimulate the formation of new blood vessels further enhancing and optimizing repair.

Other indications

SMS cells have potent cross-talk with multiple cell types that drive tissue regeneration across different organs.

They readily bind to mesenchymal stem/stromal cells (MSCs) residing in all vascularized tissues, enhancing MSC activation, and pro-repair signaling. Because MSCs play central roles in organ healing, this interaction amplifies regenerative activity wherever MSCs are present.

In addition, SMS cells exert strong effects on endothelial cells, promoting their proliferation, stabilization, and organization into new blood vessels. This angiogenic stimulation is critical for tissue repair, as restored and newly formed microvasculature provides the oxygen, nutrients, and biochemical support required for effective regeneration.

Together, these interactions position SMS cells as powerful upstream modulators of multi-organ healing through combined mesenchymal activation and vascular regeneration.

Scientist analyzing cell samples under a microscope in a regenerative medicine research laboratory.
Scientist analyzing cell samples under a microscope in a regenerative medicine research laboratory.

References

  • GBD 2021 Osteoarthritis Collaborators. (2023). Global, regional, and national burden of osteoarthritis, 1990–2020 and projections to 2050: A systematic analysis for the Global Burden of Disease Study 2021. The Lancet Rheumatology, 5(9), e508–e522.
    https://doi.org/10.1016/S2665-9913(23)00163-7
  • Hunter, D. J., & Bierma-Zeinstra, S. (2019). Osteoarthritis. The Lancet, 393(10182), 1745–1759. https://doi.org/10.1016/S0140-6736(19)30417-9
  • Luo, P., Yuan, Q., Wan, X., Yang, M., & Xu, P. (2023). Effects of immune cells and cytokines on different cells in OA. Journal of Inflammation Research, 16, 2329–2343. https://doi.org/10.2147/JIR.S413578
  • Wong, K. L., Lee, K. B., Tai, B. C., et al. (2013). Injectable cultured bone marrow–derived mesenchymal stem cells in varus knees with cartilage defects undergoing high tibial osteotomy: A prospective, randomized controlled clinical trial with 2 years’ follow-up. Arthroscopy, 29, 2020.
  • Whittle, S. L., Johnston, R. V., McDonald, S., et al. (2025). Stem cell injections for osteoarthritis of the knee. Cochrane Database of Systematic Reviews, 2025(4), CD013342.
  • Rahmo, A. (2014). Compositions and methods for using small mobile stem cells (WO 2014200940 A1). World Intellectual Property Organization.
  • Rahmo, A. (2014). Extracellular matrix protein compositions and methods for treating wounds (WO 2020068432 A1). World Intellectual Property Organization.
  • Rahmo, A. (2014). Small mobile stem cells (SMS) and uses thereof (U.S. Patent No. 10,041,037 B2). U.S. Patent and Trademark Office.
  • Rahmo, A. (2017). Compositions and methods for using small mobile stem cells (U.S. Patent No. 12,146,164 B2). U.S. Patent and Trademark Office.
  • Rahmo, A. (2021, May 26). Small mobile stem cells: Potential for multi targeted therapy of emphysema in COPD. American Academy of Stem Cell Physicians.
  • Rahmo, A. (2021). Stem cell compositions and methods of repairing tissue (WO 2021183287 A1). World Intellectual Property Organization.