
SMSbiotech Receives FDA Clearance for Inhaled Stem Cell Therapy COPD Trial
The blood-derived, off-the-shelf cells are administered directly to the lungs through a standard nebulizer, with first U.S. patient dosing targeted for late 2026.


The blood-derived, off-the-shelf cells are administered directly to the lungs through a standard nebulizer, with first U.S. patient dosing targeted for late 2026.

Regend Therapeutics plans a Phase 3, randomized, blinded, placebo-controlled study enrolling 102 people with COPD and emphysema to assess lung diffusion capacity at 52 weeks.

The company is expanding its preclinical work on acute respiratory syndrome to investigate whether its fibroblasts may help with deadly lung inflammation, vascular leakage, and tissue damage.

The partnership will support clinical and future commercial supply of RION’s exosome therapies for tissue repair and regenerative medicine.

The new grants will support diverse early-stage research projects, aiming to advance regenerative medicine tools and future therapies.

Researchers are exploring whether stem cell-derived extracellular vesicles could offer safer, targeted therapies for respiratory diseases, but technical hurdles remain.

The study will test whether induced pluripotent stem cells can help repair airway damage in people with COPD.

Researchers will test if umbilical cord stem cell infusions can safely reduce lung disease in extremely premature infants.

The Phase 2 trial RCT will evaluate adverse event and efficacy endpoints.