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

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
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• 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

• 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

Locations
United States
Ohio
Cincinnati Children's Hospital Medical Center
RECRUITING
Cincinnati
Contact Information
Primary
Celeste Dourson, MS
Celeste.Dourson@cchmc.org
513-636-7679
Backup
Jamie Wilhelm, BS
Jamie.Wilhelm@cchmc.org
513-803-1102
Time Frame
Start Date: 2021-01-27
Estimated Completion Date: 2026-06
Participants
Target number of participants: 180
Treatments
Experimental: VSTs to Prevent
VSTs are given through an IV infusion 21-30 days after transplant to see if the VSTs will help prevent a viral infection.
Experimental: VSTs to Treat
VSTs will be given only if a viral infection develops.
Related Therapeutic Areas
Sponsors
Leads: Children's Hospital Medical Center, Cincinnati
Collaborators: Hoxworth Blood Center

This content was sourced from clinicaltrials.gov