Adenovirus Infection

3

Review clinical trials related to Adenovirus Infection. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Available

TETRAVI Expanded Access Program

This Expanded Access Program (EAP) allows qualified physicians within Texas to obtain access to multivirus-specific cytotoxic T lymphocytes (VSTs) developed under Baylor College of Medicine's TETRAVI program (NCT04013802) for the treatment of persistent or recurrent infections with EBV, CMV, adenovirus, or BK virus in pediatric patients being treated in Texas who have received allogeneic stem cell transplants and have no other suitable therapeutic options.

Trial details
Age: Up to 17Biological sex: AllType: Expanded AccessSponsor: Baylor College of MedicineUpdated: Sep 15, 2026
Eligibility criteria

Patients <18 years of age. [+4]

Patients with active uncontrolled infections unrelated to the viruses mentioned. [+2]

Status: Recruiting

Pilot Study of Haploidentical Donor Adenovirus Specific T-lymphocytes to Treat Refractory Adenovirus Infections

This open-label, single-arm, phase I/II clinical trial will assess the safety and efficacy of related donor adenovirus-specific T lymphocytes isolated from whole blood or leukapheresis products. The adenovirus-specific T lymphocytes will be generated automatically by the CliniMACS Prodigy using the CliniMACS Cytokine Capture System (IFN-γ) after incubation with MACS GMP PepTivator Peptide Pools of Hexon 5 for enrichment.

Participants needed: 12
Trial details
Phase: Phase 1, Phase 2Age: Up to 60Biological sex: AllType: InterventionalSponsor: Nationwide Children's HospitalUpdated: May 13, 2025Locations: 1
Eligibility criteria

Patients who are solid organ transplantation recipients (renal, heart, lung, liv... [+11]

Receipt of anti-thymocyte globulin (ATG), alemtuzumab, cytoxan, or other T-cell... [+14]

Status: Recruiting

A Study to Assess Safety and Feasibility of Direct Infusions of Donor-derived Virus-specific T-cells in Recipients of Hematopoietic Stem Cell Transplantation With Post-transplant Viral Infections Using the Cytokine Capture System®

To assess the feasibility of donor-derived interferon (IFN)-γ positive select-ed virus-specific T-cells using the cytokine capture system® (CCS) and the safety of subsequent infusion in recipients of hematopoietic stem cell transplantation (HSCT) with treatment refractory post-transplant viral infections. The CCS has already been successfully used in clinical studies in Germany and United Kingdom (UK).

Participants needed: 30
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: University Hospital, Basel, SwitzerlandUpdated: Mar 20, 2025Locations: 1
Eligibility criteria

Adults > 18 years of age [+12]

graft-versus-host disease (GVHD) > grade 2 at the time point of planned infusion [+1]