Cytomegalovirus

4

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

Condition / disease
Location
Status: Recruiting

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

This trial studies the side effects and how well allogeneic cytomegalovirus-specific cytotoxic T lymphocytes (donor cytomegalovirus \[CMV\] specific cytotoxic T-lymphocytes \[CTLs\]) or allogeneic adenovirus-specific cytotoxic T lymphocytes (donor adenovirus-specific \[AdV\] specific CTLs) work in treating CMV or AdV reactivation or infection in participants who have undergone stem cell transplant or solid organ transplant. White blood cells from donors may be able to kill cancer cells in patients with cytomegalovirus or adenovirus that has come back after a stem cell or solid organ transplant.

Participants needed: 20
Trial details
Phase: Early Phase 1Age: 1-85Biological sex: AllType: InterventionalSponsor: Sumithira VasuUpdated: Apr 15, 2026Locations: 2
Eligibility criteria

Patients must have solid organ transplant or have received allogeneic hematopoie... [+18]

Receipt of anti-thymocyte globulin (ATG), alemtuzumab, or other T-cell depleting... [+8]

Status: Recruiting

Haplo-identical Viral-Specific T-cells for Treatment of Cytomegalovirus and Adenovirus Infections After Hematopoietic Cell Transplantation

The investigators want to learn if CMV- and ADV-specific T-cells (cells that fight infections) isolated (selected) from a donor using an automated medical device can be a safe treatment for treating patients with CMV, and ADV after transplant.This study will test the effects and safety of giving VSTs produced here at St. Jude in treating the participant's infection. Primary objective To determine the efficacy of VSTs to achieve a ≥1 log10 reduction in CMV and/or ADV viral load in the peripheral blood 4 weeks after VST infusion. When the initial viral load is \<1 log10 above the threshold of detection, the objective is to achieve a reduction to below the threshold of detection. Secondary objectives * Determine the safety of VSTs when used to treat CMV and/or ADV viremia post-HCT. * Determine the proportion of patients who achieve a negative viral load at 3 months post-infusion. * Assess the persistence of response for 6 months post-infusion.

Participants needed: 42
Trial details
Phase: Phase 2Age: Up to 18Biological sex: AllType: InterventionalSponsor: St. Jude Children's Research HospitalUpdated: Feb 23, 2026Locations: 1
Eligibility criteria

Patients who have undergone haploidentical HCT or a matched-sibling/matched-unre... [+20]

Active GVHD. [+6]

Status: Recruiting

Risk Assessment of Community Spread of Multiple Endemic Infectious Diseases in a One Health Perspective

RACSMEI addresses the high burden of infectious diseases in low- and middle-income countries, including Cambodia, where limited surveillance and laboratory capacity often obscure etiologies and transmission dynamics. This knowledge gap hinders the design of effective prevention and control strategies. RACSMEI will improve understanding across multiple pathogens using a multidisciplinary One Health approach. We will answer key questions on burden, ecology, transmission and population immune status to inform targeted and culturally appropriate interventions. The project combines a nationally representative One Health survey, social-science methods, and multiplex, diverse diagnostics to efficiently test for 57 priority pathogens, including zoonotic and vector-borne agents, vaccine-preventable and elimination-targeted diseases, enteric, respiratory, and environmentally transmitted pathogens and selected neglected tropical diseases and parasites relevant to Cambodia. Mathematical modelling will reconstruct and forecast transmission dynamics and assess the potential impact of future public-health strategies. By integrating intersectoral data and innovative methods, RACSMEI will generate actionable evidence for public-health authorities, support precision One Health interventions, and help reduce disease burden in affected communities. The project also aims to ensure the transferability of methods and insights to other countries facing similar challenges.

Participants needed: 10,000
Trial details
Age: 2-75Biological sex: AllType: ObservationalSponsor: Institut Pasteur du CambodgeUpdated: Jan 22, 2026Locations: 1
Eligibility criteria

Residency in the village for more than 6 months; [+3]

Unable to understand or consent; [+3]

Status: Recruiting

Strategic Help With Immunoglobulin to Enhance Protect Against Late Disease (CMV)

This study is being done to find out if administering CytoGam® after the end of standardly prescribed preventive antiviral treatment can help transplant recipients with a high risk for developing late CMV disease after a liver and/or kidney transplant.

Participants needed: 80
Trial details
Phase: Phase 4Age: 18-75Biological sex: AllType: InterventionalSponsor: Camille N. Kotton, MDUpdated: Dec 22, 2025Locations: 2
Eligibility criteria

High risk pretransplant CMV donor seropositive/recipient seronegative (D+R-) kid... [+3]

Any pre-transplant CMV serologic combinations besides CMV D+/R- [+14]