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Virus-specific T-cell Immunity for the Treatment of Some Resistant Viral Infections After Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-518925-14-02
Acronym
PTC:VS-TC
Enrollment
10
Registered
2025-01-31
Start date
2024-07-17
Completion date
Unknown
Last updated
2025-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adenovirus, EBV) resistant to pharmacological therapies., Patients who have received an allogeneic haematopoietic stem cell transplant and who have developed post-transplant viral reactivation (CMV

Brief summary

Adverse events: To collect any adverse event defined as any significant alteration of vital signs and / or organ function, expressed in clinical, hematochemical and radiological findings according to version 5 of the Common Terminology Criteria for Adverse Events (CTCAE)

Detailed description

Organ damage; overall survival; specific cell viral immunity; variation of viremia.

Interventions

None listed

Sponsors

IRCCS Istituto Giannina Gaslini
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Adverse events: To collect any adverse event defined as any significant alteration of vital signs and / or organ function, expressed in clinical, hematochemical and radiological findings according to version 5 of the Common Terminology Criteria for Adverse Events (CTCAE)

Secondary

MeasureTime frame
Organ damage; overall survival; specific cell viral immunity; variation of viremia.

Countries

Italy

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026