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Enrolling By InvitationNCT07474051

Long-Term Follow-Up of AvenCell Sponsored CAR-T Cell Clinical Trials

Persistence Evaluation and Response Study for Immunotherapy Safety Tracking of Participants Who Receive an AvenCell CAR-T Cell Therapy

Status
Enrolling By Invitation
Phase
Study type
Observational
Enrollment
178 (estimated)
Sponsor
AvenCell Therapeutics, Inc. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The goal of this clinical study is to learn more about the long-term safety, effectiveness and prolonged action of patients who participated in an AvenCell-sponsored clinical trial and received treatment with AvenCell's UniCAR or RevCAR platforms.

Detailed description

To assess the incidence and severity of delayed serious adverse events (SAEs) possibly related to AVC-CAR-T cell therapy and AEs of special interest (AESIs), including secondary malignancies, neurologic disorders, rheumatologic or other autoimmune disorders, newly diagnosed serious hematologic disorders, severe infections, as well as pregnancy and newborn health complications where observed.

Conditions

Interventions

TypeNameDescription
BIOLOGICALUniCAR02-T (IMP) With Targeting Module TM123No investigational product will be administered
BIOLOGICALUniCAR02-T-pPSMANo investigational product will be administered
BIOLOGICALAllo-RevCAR01- T with Targeting Module R-TM123No investigational product will be administered
BIOLOGICALAllo-QuadCAR01-TNo investigational product will be administered

Timeline

Start date
2026-01-29
Primary completion
2040-11-30
Completion
2041-01-30
First posted
2026-03-16
Last updated
2026-03-16

Locations

5 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT07474051. Inclusion in this directory is not an endorsement.