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A Long-Term Follow-Up Observational Study to Evaluate Safety in Subjects Who Have Received a Gene-Modified Regulatory T Cell (Treg) Therapeutic

NCT07123038

This study is recruiting at 7 US sites in 4 states, according to its ClinicalTrials.gov record last updated .

Summary

To assess the emergence, type, severity, and potential causality of delayed adverse events following administration of a gene-modified Treg therapeutic.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Rheumatoid Arthritis (RA)
  • Hidradenitis Suppurativa (HS)

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 to 71 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Sonoma Biotherapeutics, Inc.
Last updated on ClinicalTrials.gov
April 16, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 2

  • UCSF Medical Center · San Francisco, CA
  • Stanford Medical Center · Stanford, CA

Colorado · 1

  • University of Colorado · Aurora, CO

Illinois · 1

  • Northwestern University · Chicago, IL

Massachusetts · 3

  • Brigham and Women's Hospital · Boston, MA
  • Massachusetts General Hospital · Boston, MA
  • Tufts University · Boston, MA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.