NCT06027879

Anti-viral T-cell Therapy by Gamma Capture

Enrolling by Invitation
PHASE1Ages 1–65InterventionalTreatment
Paul Szabolcs
~25 participants
Updated 2026-06-29 on ClinicalTrials.gov
What's tested:Specific T- Lymphocytes

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Grade III-IV Acute GvHD
Measured over Day 0
+18 more outcomes measured
Adenovirus
Cytomegalovirus Infections
Epstein-Barr Virus Infections
1 sites across 1 states
Pennsylvania1
  • Paul Szabolcs, MD · PRINCIPAL_INVESTIGATOR · University of Pittsburgh

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Grade III-IV Acute GvHDDay 0

    The number of patients who develop Grade III-IV acute graft versus host disease (GVHD) attributed to the viral specific T cells.

  • Grade III-IV Acute GvHD1 month from first cellular infusion

    The number of patients who develop Grade III-IV acute graft versus host disease (GVHD) attributed to the viral specific T cells.

  • Grade III-IV Acute GvHD3 month from first cellular infusion

    The number of patients who develop Grade III-IV acute graft versus host disease (GVHD) attributed to the viral specific T cells.

  • Grade III-IV Acute GvHD6 month from first cellular infusion

    The number of patients who develop Grade III-IV acute graft versus host disease (GVHD) attributed to the viral specific T cells.

  • Clinical response to treatment of viral infection1 month from first cellular infusion

    Rate of Elimination or reduction of oxygen dependence identified at baseline

  • Clinical response to treatment of viral infection1 month from first cellular infusion

    Rate of Resolution of diarrhea attributable to the viral disease, less than 4 stools daily

  • Clinical response to treatment of viral infection1 month from first cellular infusion

    Rate of Resolution of fever, attributable to viral disease

  • Clinical response to treatment of viral infection1 month from first cellular infusion

    Rate of Resolution or improvement of radiographic findings attributable to viral disease

  • Clinical response to treatment of viral infection1 month from first cellular infusion

    Rate of Resolution or improvement of lymphadenopathy attributable to EBV, and ophthalmic findings attributable to CMV retinitis

  • Clinical response to treatment of viral infection3 month from first cellular infusion

    Rate of Elimination or reduction of oxygen dependence identified at baseline

  • Clinical response to treatment of viral infection3 month from first cellular infusion

    Rate of Resolution of diarrhea attributable to the viral disease, less than 4 stools daily

  • Clinical response to treatment of viral infection3 month from first cellular infusion

    Rate of Resolution of fever, attributable to viral disease

  • Clinical response to treatment of viral infection3 month from first cellular infusion

    Rate of Resolution or improvement of radiographic findings attributable to viral disease

  • Clinical response to treatment of viral infection3 month from first cellular infusion

    Rate of Resolution or improvement of lymphadenopathy attributable to EBV, and ophthalmic findings attributable to CMV retinitis

  • Clinical response to treatment of viral infection6 months from first cellular infusion

    Rate of Elimination or reduction of oxygen dependence identified at baseline

  • Clinical response to treatment of viral infection6 months from first cellular infusion

    Rate of Resolution of diarrhea attributable to the viral disease, less than 4 stools daily

  • Clinical response to treatment of viral infection6 months from first cellular infusion

    Rate of Resolution of fever, attributable to viral disease

  • Clinical response to treatment of viral infection6 months from first cellular infusion

    Rate of Resolution or improvement of radiographic findings attributable to viral disease

  • Clinical response to treatment of viral infection6 months from first cellular infusion

    Rate of Resolution or improvement of lymphadenopathy attributable to EBV, and ophthalmic findings attributable to CMV retinitis