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Phase 1 Stem Cell Trial, Systemic Sclerosis, Apr 2026

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Summary

NIH registered a Phase 1 clinical trial (NCT07542067) evaluating allogeneic stromal mesenchymal stem cells derived from Wharton's jelly in patients with diffuse cutaneous systemic sclerosis and refractory pulmonary involvement. The single-site study, expected to begin April 2026, will assess safety and preliminary efficacy of intravenous stem cell infusion in a patient population with limited therapeutic alternatives and poor survival prognosis.

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What changed

NIH added a new Phase 1 clinical trial registration for a stem cell therapy study targeting systemic sclerosis patients with pulmonary complications. The trial will use allogeneic stromal mesenchymal cells from Wharton's jelly administered via intravenous infusion. The study population comprises patients refractory to conventional DMARD and cyclophosphamide therapy.

For sponsors and clinical investigators, this registry entry signals ongoing research interest in cell-based therapies for rare autoimmune conditions with pulmonary involvement. Healthcare providers treating systemic sclerosis patients may wish to identify potential trial candidates and monitor outcomes data as the study progresses.

Archived snapshot

Apr 22, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

Infusion of Allogeneic Stromal Mesenchymal Stem Cells From Wharton´s Jelly in Patients With Diffuse Cutaneous Systemic Sclerosis With Refractory Pulmonary Involvement to Treatment

Phase 1 NCT07542067 Kind: PHASE1 Apr 21, 2026

Abstract

Progressive SSc is an entity with limited therapeutic alternatives and a survival rate of less than 45% within the first 3 to 5 years. The disease causes severe limitations in quality of life, ranging from functional impairment to depression. Up to 20% of patients become refractory to conventional treatment with disease-modifying anti-rheumatic drugs (DMARDs) and cyclophosphamide therapy. This condition favors progression to visceral involvement, including gastrointestinal, pulmonary, and pulmonary hypertension manifestations. The latter, considered a poor prognostic factor, increases mortality in this patient population and drastically affects quality of life. For this reason, different therapeutic options have been considered, including cell transplantation and stem cell use.

Among the options studied to date are stromal mesenchymal cells derived from Wharton's jelly. These cells have been administered via intravenous infusion or direct application in various disease scenarios, ranging from vascular involvement to interstitial lung disease and pulmonary hypertension, with promising results in terms of clinical progression, quality of life improvement, and prognostic indices. This therapy has demonstrated a favorable safety profile at the time of administration and a low rate of adverse events, with self-limiting fever being the most frequent event.

Based on the above and considering the possibility of offering patients without therapeutic alternatives for the disease, ...

Conditions: Systemic Sclerosis Pulmonary, Pulmonary Hypertension, Pulmonary Fibrosis

Interventions: Mesenchymal Stem Cells from Wharton´s jelly

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Classification

Agency
NIH
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Clinical investigators Healthcare providers Patients
Industry sector
6211 Healthcare Providers
Activity scope
Clinical trial registration Stem cell therapy research
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Pharmaceuticals Public Health

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