Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02136797 · ClinicalTrials.gov registry record · Phase 2

Trial of Third Party Donor Derived CMVpp65 Specific T-cells for The Treatment of CMV Infection or Persistent CMV Viremia After Allogeneic Hematopoietic Stem Cell Transplantation

A Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 2
Development phase
77
Enrollment target

NCT02136797: Completed Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT02136797 is a Phase 2 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 77 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT02136797, a Phase 2 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
77 participants
Enrollment target

Study Summary

The purpose of this study is to see how well transfusions of T-cells work in treating CMV. Tcells are a type of white blood cell that helps protect the body from infection. A transfusion is the process by which blood from one person is transferred to the blood of another. In this case, the T-cells are made from the blood of donors who are immune to CMV. The T-cells are then grown and taught to attack the CMV virus in a lab.

Primary Outcome

defined as the clearance of the CMV infection 3-7 weeks following completion of the last cycle of CMV CTLs.

Interventions

  • BIOLOGICAL CMVpp65 Specific T-cells

Trial Details

FieldValue
Enrollment Target 77 participants
Start Date 2014-05-08
Est. Completion 2024-02-08
Phase Phase 2
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT02136797 record still lists

NCT02136797 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 77 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 1 intervention - of which CMVpp65 Specific T-cells is the first listed.

NCT02136797 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02136797 about?

NCT02136797 is a clinical study titled "Trial of Third Party Donor Derived CMVpp65 Specific T-cells for The Treatment of CMV Infection or Persistent CMV Viremia After Allogeneic Hematopoietic Stem Cell Transplantation". The purpose of this study is to see how well transfusions of T-cells work in treating CMV. Tcells are a type of white blood cell that helps protect the body from infection. A transfusion is the process by which blood from one person is transferred to the blood of another. In this case, the T-cells a...

What is the current status of trial NCT02136797?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 77 participants. The study started on 2014-05-08. Estimated completion is 2024-02-08.

What interventions are being tested in trial NCT02136797?

The interventions under investigation include: CMVpp65 Specific T-cells (BIOLOGICAL).

Who is sponsoring clinical trial NCT02136797?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02136797's enrollment target sits among peer trials

77 891st of 2000 higher than 1,108 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02127398 · 77 participants · Phase 2

    Stool Transplants to Treat Refractory Clostridium Difficile Colitis

  • NCT04159103 · 77 participants · Phase 1

    Open-Label Study of mRNA-3927 in Participants With Propionic Acidemia

  • NCT04683003 · 77 participants · Phase 3

    A Study of TAK-755 in Participants With Congenital Thrombotic Thrombocytopenic Purpura

  • NCT05004116 · 77 participants · Phase 1

    A Study of Repotrectinib in Combination With Chemotherapy in Children and Young Adults With Solid Tumor Cancer

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02136797, the US trial registry maintained by the National Library of Medicine. NCT02136797 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.