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NCT Number: NCT04230356

Trial of Scheduled Versus Treatment Administration of Donor-Derived Viral Specific T-cells for Viral Infections After Stem Cell Transplant

The purpose of this research study is to learn more about the use of viral specific T-lymphocytes (VSTs) to prevent or treat viral infections that may happen after allogeneic stem cell transplant. Allogeneic means the stem cells come from another person. VSTs are cells specially designed to fight viral infections that may happen after a stem cell transplant (SCT).

Stem cell transplant reduces the body's ability to fight infections. Viral infections are a common problem after transplant and can cause significant complications. Moreover, treatment of viral infections is expensive and time consuming, with families often administering prolonged treatments with intravenous anti-viral medications, or patients requiring prolonged admissions to the hospital. The medicines can also have side effects like damage to the kidneys or reduction in the blood counts, so in this study the investigators are trying to find a better way to treat these infections.

Recruiting

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, 45229, United States

Location status: Recruiting

Location contact

Celeste Dourson, MS

CONTACT

[email protected]

513-636-7679

Stella Davies, MBBS, PhD

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

SCHEDULED ARM:

Inclusion criteria

  • Recipient must be at least 21 days after stem cell infusion
  • Clinical status must allow tapering of any steroids to < 0.5mg/kg prednisone or other steroid equivalent
  • No critical illness making VST infusion hazardous

Exclusion criteria

  • Active acute GVHD grades II-IV.
  • Uncontrolled relapse of malignancy.
  • Infusion of ATG or alemtuzumab within 2 weeks prior to VST infusion. Alemtuzumab levels will be collected in the second week following stem cell infusion in patients who received alemtuzumab as part of their conditioning regimen. The level must be less than or equal to 0.15 prior to infusion of VSTs. In patients with level greater than 0.15, alemtuzumab levels can be checked serially until a level ≤ 0.15 is obtained. They would become eligible for scheduled VST infusion at that point.

TREATMENT ARM

Inclusion criteria

  • Blood adenovirus PCR ≥1,000
  • Blood CMV PCR ≥ 500
  • Blood EBV PCR ≥ 9,000
  • Plasma BKV PCR >1,000
  • Evidence of invasive adenovirus infection. Adenovirus infection will be defined as the presence of adenoviral positivity as detected by PCR or culture from one site such as stool or blood or urine or nasopharynx. Adenovirus disease will be defined as the presence of adenoviral positivity as detected by culture or PCR from more than 2 sites such as stool or blood or urine or nasopharynx.
  • Evidence of invasive CMV infection, defined as pneumonitis, retinitis, colitis, hepatitis
  • Evidence of EBV-associated lymphoproliferation (EBV-LPD) defined as proven EBV-LPD by biopsy or probable EBV-LPD defined as an elevated EBV DNA level in the blood associated with clinical symptoms (adenopathy or fever or masses on imaging) but without biopsy confirmation.
  • Evidence of symptomatic BK virus infection, defined as hemorrhagic cystitis or BK nephropathy.
  • No active acute GVHD grades II-IV
  • No uncontrolled relapse of malignancy
  • No infusion of ATG or alemtuzumab within 2 weeks of VST infusion.
  • Clinical status must allow tapering of any steroids to < 0.5mg/kg prednisone or other steroid equivalent

Treatment and study plan

Viral Specific T-cells (VSTs) Scheduled

Biological

VSTs will be infused into stem cell transplant recipients on schedule.

Viral Specific T-cells (VSTs) Treatment

Biological

VSTs will be infused into stem cell transplant recipients only if viremia is detected.

Primary outcomes

  1. Number of Treatment Failures

    Time frame: 21 - 100 days after transplant

    Treatment failure is defined as EBV>100,000, BKV >100,000, CMV >5,000 or Adv >50,000 at any time post randomization.

Study contacts

Contact information is provided by the study sponsor or research team.

Celeste Dourson, MS

CONTACT

[email protected]

513-636-7679

Jamie Wilhelm, BS

CONTACT

[email protected]

513-803-1102

Sponsors and collaborators

Lead sponsor

Children's Hospital Medical Center, Cincinnati

Other

Collaborators

  • Hoxworth Blood Center

Registry information

Official study title

A Randomized Trial of Scheduled Versus Treatment Administration of Donor-Derived Viral Specific T-cells (VSTs) for Control of Viral Infections After Allogeneic Stem Cell Transplant

Important dates

Study start
2021
Primary completion
2028
Study completion
2028
First posted
Jan 18, 2020
Registry last updated
Mar 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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