Adenovirus Infection

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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: Recruiting

Antigen-specific Cytotoxic T Cells in the Treatment of Opportunistic Infections

Epstein Barr Virus (EBV) or Cytomegalovirus (CMV) infection results in significant morbidity and mortality in hematopoietic stem cell transplantation (HSCT) patients. HSCT patients often face opportunistic infections due to the immunosuppressive state during transplantation. Antimicrobial drugs are usually used for prophylactic purposes and for treatment after early detectable infections. Unfortunately, some patients develop resistance to such drug treatment. In addition to HSCT patient, immune compromised patient may also be victim to opportunistic infections. Many infections can be effectively managed by functional immune recovery. In this study, the safety and efficacy of microbial-specific cytotoxic T lymphocytes (CTLs) will be investigated.

Participants needed: 100
Trial details
Phase: Phase 1, Phase 2Age: 6-80Biological sex: AllType: InterventionalSponsor: Shenzhen Geno-Immune Medical InstituteUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Evidence of CMV, EBV, ADV, BKV or known pathogen infection (viral DNA, immunohis... [+13]

Subject infected with HCV (HCV antibody positive), HBV (HBsAg positive), HIV (HI... [+5]

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: Aug 5, 2025
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]