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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

Recruitingn/aAges 18 Years - 71 YearsAllSonoma Biotherapeutics, Inc.
NCT07123038 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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

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📋 Eligibility rules (as published)
Inclusion Criteria: * Subject was previously administered at least 1 dose of a Sonoma Biotherapeutics, Inc. gene-modified Treg therapeutic in a prior parent treatment protocol. * Subject understands the purpose and risks of the study and is willing to provide written informed consent. * Subject is willing to comply with all study procedures for the follow-up period. Exclusion Criteria: * Participation in the study is not in the subject's best interest, in the opinion of the Investigator
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What it tests

  • Long Term Safety Monitoring Procedures
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Where

10 sites
UCSF Medical Center
San Francisco, United States
Stanford Medical Center
Stanford, United States
University of Colorado
Aurora, United States
Northwestern University
Chicago, United States
Tufts University
Boston, United States
Massachusetts General Hospital
Boston, United States
Brigham and Women's Hospital
Boston, United States
University of Minnesota
Minneapolis, United States

…and 2 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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