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Long Term Follow-up Observational Study in Patients Treated with Gene-Modified T-Cell Therapy

Long Term Follow-up Observational Study in Patients Treated with Gene-Modified T-Cell Therapy

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06825845
Enrollment
1500
Registered
2025-02-13
Start date
2025-03-31
Completion date
2040-06-30
Last updated
2025-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed or Refractory Multiple Myeloma

Brief summary

This is a prospective long-term follow-up (LTFU) study to evaluate the long-term safety and survival benefit for patients who received at least one of CARsgen's GM T cell product in a clinical trial or as a commercially available product. In this study, patients will be followed for up to 15 years after last GM T-cell infusion for the evaluation of delayed adverse events (AEs), vector persistence, potential risk for integration, and survival time due to GM T-cell exposure.

Detailed description

As recommended by Health Authorities guidelines for human gene therapy products containing an integrated transgene, during the LTFU for 15 years after infusion, the information of the enrolled patients will be collected, including medical history, physical and laboratory-related examination data, AEs, survival information, etc. AEs recorded will include new malignancy, new or exacerbation infection, new or exacerbation neurological disease, new or exacerbation autoimmune disease etc. Samples will be obtained according to the schedule of activities, and laboratory tests will be conducted or preserved for future use. All participants are recommended to be followed at least every six months for the first 5 years, and annually from the 6th year until at least 15 years or until informed consent withdrawal, loss to follow-up, or death, whichever occurs first.

Interventions

Non-intervention

Sponsors

CARsgen Therapeutics Co., Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

\- 1. All patients who have received at least one GM T-cell infusion in the parent clinical study or in the post-approval setting. 2\. Patients must be capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol. For patients incapable of providing consent, the signed ICF of their legally accepted guardians must be obtained.

Exclusion criteria

* There are no specific

Design outcomes

Primary

MeasureTime frame
To assess the risk of delayed AEs following exposure to GM T cells15 years

Contacts

Primary ContactYajing Zhang
23975701@qq.com18601333856

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026