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

NCT00509691 · ClinicalTrials.gov registry record · Phase 1

Vaccine Therapy in Treating Patients Who Have Undergone a Donor Stem Cell Transplant and Have Cytomegalovirus Infection That Has Not Responded to Therapy

A Phase 1 study of Cancer, sponsored by University of Louisville.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target
1
Study location

NCT00509691: Completed Phase 1 study of Cancer, sponsored by University of Louisville.

NCT00509691 is a Phase 1 study of Cancer that has completed, run by University of Louisville. The registered enrollment target is 20 participants, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00509691, a Phase 1 study of Cancer, has completed, sponsored by University of Louisville.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

RATIONALE: Vaccines may help the body build an effective immune response to kill cytomegalovirus infections. PURPOSE: This phase I trial is studying the side effects and best dose of vaccine therapy in treating patients who have undergone a donor stem cell transplant and have cytomegalovirus infection that has not responded to therapy.

Conditions Studied

Interventions

  • GENETIC polymerase chain reaction
  • OTHER flow cytometry
  • OTHER diagnostic laboratory biomarker analysis
  • OTHER immunologic technique
  • BIOLOGICAL cytomegalovirus pp65-specific cytotoxic T lymphocytes

Study Locations (1)

Pennsylvania

  • Penn State Hershey Cancer Institute at Milton S. Hershey Medical Center - Hershey

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2007-06
Est. Completion 2011-12
Phase Phase 1
University of Louisville

217 total trials

What the finished NCT00509691 record still lists

NCT00509691 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Cancer appearing as the primary indexed condition, and to 5 interventions - of which polymerase chain reaction is the first listed.

NCT00509691 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00509691 about?

NCT00509691 is a clinical study titled "Vaccine Therapy in Treating Patients Who Have Undergone a Donor Stem Cell Transplant and Have Cytomegalovirus Infection That Has Not Responded to Therapy". RATIONALE: Vaccines may help the body build an effective immune response to kill cytomegalovirus infections. PURPOSE: This phase I trial is studying the side effects and best dose of vaccine therapy in treating patients who have undergone a donor stem cell transplant and have cytomegalovirus infect...

What is the current status of trial NCT00509691?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2007-06. Estimated completion is 2011-12.

What conditions does trial NCT00509691 study?

This clinical trial studies the following conditions: Cancer.

What interventions are being tested in trial NCT00509691?

The interventions under investigation include: polymerase chain reaction (GENETIC), flow cytometry (OTHER), diagnostic laboratory biomarker analysis (OTHER), immunologic technique (OTHER), cytomegalovirus pp65-specific cytotoxic T lymphocytes (BIOLOGICAL).

Who is sponsoring clinical trial NCT00509691?

This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00509691 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00509691's enrollment target sits among peer trials

20 561st of 615 higher than 47 of 615 other Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cancer 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

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00509691, the US trial registry maintained by the National Library of Medicine. NCT00509691 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.