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Study details
Enrolling now

Donor Virus-Specific CMV or AdV CTL to Treat CMV or AdV Reactivation or Disease After Solid Organ or HCT

Sumithira Vasu
NCT IDNCT03665675ClinicalTrials.gov data as of Apr 2026
Phase

EARLY_PHASE1

Target enrollment

20

Study length

about 5.5 years

Ages

1–85

Locations

2 sites in OH

What this study is about

This trial is testing if donor virus-specific cytotoxic T lymphocytes (CTLs) can treat cytomegalovirus (CMV) or adenovirus (AdV) reactivation or infection in people who have had a stem cell transplant or solid organ transplant. White blood cells from donors may be able to kill cancer cells in patients with CMV or AdV that has come back after a stem cell or solid organ transplant.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive Allogeneic Adenovirus-specific Cytotoxic T Lymphocytes
  • 2.Receive Allogeneic Cytomegalovirus-Specific Cytotoxic T lymphocytes

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Incidence of adverse events defined by the National Cancer Institute Common Terminology Criteria for Adverse Events 4.0

Secondary: Antiviral activity defined as response to viral load, Number of participants with treatment-related adverse events as assessed by CTCAE v4.0., Overall survival