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A Study to Evaluate Tabelecleucel in Participants With Epstein Barr Virus (EBV) Associated Diseases
NCT04554914 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to assess the efficacy and safety of tabelecleucel in participants with EBV-associated diseases.
Conditions Studied
Interventions
- BIOLOGICAL Tabelecleucel
Study Locations (20)
California
- University of California Los Angeles (UCLA) (Adults and Pediatrics) — Los Angeles
- Children's Hospital of Orange County (Pediatrics [up to 25 years old]) — Orange
- Lucile Packard Children's Hospital Stanford (Pediatrics only) — Palo Alto
- University of California Davis Comprehensive Cancer Center (Adults and Pediatrics) — Sacramento
New York
- Columbia University Irving Medical Center (Adults only) — New York
- Memorial Sloan-Kettering Cancer Center (Adults and Pediatrics) — New York
- The Children's Hospital at Montefiore (Adults and Pediatrics) — The Bronx
Florida
- Sylvester Comprehensive Cancer Center/ University of Miami — Miami
- Moffit Cancer Center (Adults only) — Tampa
Georgia
- Children's Healthcare of Atlanta (Pediatrics only [up to 25 years old]) — Atlanta
- Emory University/Winship Cancer Institute (Adults [>= 16 years]) — Atlanta
Ohio
- Cleveland Clinic Taussig Cancer Center (Adults and Pediatrics) — Cleveland
- The Ohio State University - The James Cancer Hospital and Solove Research Institute (Adults only) — Columbus
Illinois
- Ann & Robert H. Lurie Children's Hospital of Chicago (Pediatrics only) — Chicago
Maryland
- University of Maryland Medical Center (Adults only) — Baltimore
Massachusetts
- Dana Farber Cancer Institute (DFCI) (Adults and Pediatrics) — Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 190 participants |
| Start Date | 2021-07-14 |
| Est. Completion | 2028-05 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04554914
The ClinicalTrials.gov registry entry for NCT04554914 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 190 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pierre Fabre Medicament, which has 33 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 10 conditions, with Stem Cell Transplant Complications appearing as the primary indexed condition, and to 1 intervention — of which Tabelecleucel is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04554914 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, New York, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04554914 about?
NCT04554914 is a clinical study titled "A Study to Evaluate Tabelecleucel in Participants With Epstein Barr Virus (EBV) Associated Diseases". The purpose of this study is to assess the efficacy and safety of tabelecleucel in participants with EBV-associated diseases.
What is the current status of trial NCT04554914?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 190 participants. The study started on 2021-07-14. Estimated completion is 2028-05.
What conditions does trial NCT04554914 study?
This clinical trial studies the following conditions: Stem Cell Transplant Complications, Lymphoproliferative Disorders, Solid Organ Transplant Complications, Allogeneic Hematopoietic Cell Transplant, Epstein-Barr Virus (EBV)-Associated Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04554914?
The interventions under investigation include: Tabelecleucel (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04554914?
This trial is sponsored by Pierre Fabre Medicament, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04554914 being conducted?
This trial has 20 study locations across California, Florida, Georgia, Illinois, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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