Follow-Up for Study Participants Treated With an Allogeneic CAR T-Cell Product

NCT ID: NCT06925685

Last Updated: 2025-04-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-01-31

Study Completion Date

2039-01-31

Brief Summary

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An observational, long-term follow up (LTFU) study of participants who received an allogeneic CAR T product in a prior clinical study. Participants will be followed for 15 years after their last infusion of an allogenic CAR T cell product.

Detailed Description

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Conditions

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Hematologic Malignancies Solid Tumors

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Received an allogenic CAR T-cell product infusion to treat an oncologic condition in a previous Allogene or Servier sponsored clinical study

Exclusion Criteria

* Less than 12 months of follow up after the last allogeneic CAR T-cell product, unless approved by the Allogene Medical Monitor
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Allogene Therapeutics

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Allogene Study Director

Role: STUDY_DIRECTOR

Allogene Therapeutics, Inc.

Locations

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Circuit Clinical

Buffalo, New York, United States

Site Status

Countries

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United States

Other Identifiers

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ALLO-LTFU-101

Identifier Type: -

Identifier Source: org_study_id

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