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Enrolling by invitation No phase listed Observational

Long Term Follow-up Study for Subjects Administered CLBR001

ClinicalTrials.gov ID: NCT06882317

Public ClinicalTrials.gov record NCT06882317. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 22, 2026, 6:21 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study to Evaluate the Long Term Safety of CLBR001, a Lentiviral Based Chimeric Antigen Receptor, in Subjects Previously Administered CLBR001

Study identification

NCT ID
NCT06882317
Recruitment status
Enrolling by invitation
Study type
Observational
Phase
Not listed
Lead sponsor
Calibr, a division of Scripps Research
Other
Enrollment
40 participants

Conditions and interventions

Interventions

  • Long Term Follow-Up Other

Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 27, 2025
Primary completion
Jan 31, 2044
Completion
Jan 31, 2044
Last update posted
Apr 7, 2026

2025 – 2044

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
Indiana University Melvin and Bren Simon Comprehensive Cancer Center Indianapolis Indiana 46202
Virtual Research Group- Premier Research Morrisville North Carolina 27560
University of Virginia Charlottesville Virginia 22908

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06882317, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 7, 2026 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06882317 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →