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NCT07123038 · ClinicalTrials.gov registry record
A Long-Term Follow-Up Observational Study to Evaluate Safety in Subjects Who Have Received a Gene-Modified Regulatory T Cell (Treg) Therapeutic
A clinical trial of Rheumatoid Arthritis (RA) and Hidradenitis Suppurativa (HS), sponsored by Sonoma Biotherapeutics.
- Recruiting
- Registry status
- 36
- Enrollment target
- 10
- Study locations
NCT07123038 is a study of Rheumatoid Arthritis (RA) and Hidradenitis Suppurativa (HS) that is actively recruiting participants, run by Sonoma Biotherapeutics. The registered enrollment target is 36 participants, below the 266-participant average among 17 other Rheumatoid Arthritis (RA) trials with a reported enrollment target (86% lower). The trial reports 10 study locations across 7 states.
The verdict
NCT07123038, a study of Rheumatoid Arthritis (RA) and Hidradenitis Suppurativa (HS), is actively recruiting participants, sponsored by Sonoma Biotherapeutics.
- RECRUITING
- Registry status
- 36 participants
- Enrollment target
- 10
- Study locations
Study Summary
To assess the emergence, type, severity, and potential causality of delayed adverse events following administration of a gene-modified Treg therapeutic.
Conditions Studied
Interventions
- OTHER Long Term Safety Monitoring Procedures
Study Locations (10)
Massachusetts
- Tufts University - Boston
- Massachusetts General Hospital - Boston
- Brigham and Women's Hospital - Boston
California
- UCSF Medical Center - San Francisco
- Stanford Medical Center - Stanford
Colorado
- University of Colorado - Aurora
Illinois
- Northwestern University - Chicago
Minnesota
- University of Minnesota - Minneapolis
North Carolina
- Duke University - Durham
Texas
- The University of Texas MD Anderson Cancer Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2025-07-22 |
| Est. Completion | 2040-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07123038
The ClinicalTrials.gov registry entry for NCT07123038 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 266-participant average among 17 other Rheumatoid Arthritis (RA) trials with a reported enrollment target (86% lower). The listed sponsor is Sonoma Biotherapeutics, which has 4 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Rheumatoid Arthritis (RA) appearing as the primary indexed condition, and to 1 intervention - of which Long Term Safety Monitoring Procedures is the first listed.
NCT07123038 reports 10 study locations spanning 7 distinct geographic areas - top geographies include Massachusetts, California, Colorado.
Frequently Asked Questions
What is clinical trial NCT07123038 about?
NCT07123038 is a clinical study titled "A Long-Term Follow-Up Observational Study to Evaluate Safety in Subjects Who Have Received a Gene-Modified Regulatory T Cell (Treg) Therapeutic". To assess the emergence, type, severity, and potential causality of delayed adverse events following administration of a gene-modified Treg therapeutic.
What is the current status of trial NCT07123038?
This trial is currently recruiting. The enrollment target is 36 participants. The study started on 2025-07-22. Estimated completion is 2040-12.
What conditions does trial NCT07123038 study?
This clinical trial studies the following conditions: Rheumatoid Arthritis (RA), Hidradenitis Suppurativa (HS).
What interventions are being tested in trial NCT07123038?
The interventions under investigation include: Long Term Safety Monitoring Procedures (OTHER).
Who is sponsoring clinical trial NCT07123038?
This trial is sponsored by Sonoma Biotherapeutics, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07123038 being conducted?
This trial has 10 study locations across California, Colorado, Illinois, Massachusetts, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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