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Study of Posoleucel (ALVR105,Viralym-M) for Multi-Virus Prevention in Patients Post-Allogeneic Hematopoietic Cell Transplant
Trial Status: administratively complete
This is a Phase 3 study to evaluate posoleucel (ALVR105, Viralym-M); an allogeneic,
off-the-shelf multi-virus specific T cell therapy that targets six viral pathogens: BK
virus, cytomegalovirus, adenovirus, Epstein-Barr virus, human herpesvirus 6 and JC virus.
Inclusion Criteria
Any age at the day of screening visit.
No known or suspected clinically significant disease from AdV, BKV, CMV, EBV, HHV-6, and/or JCV
Within 25 days of receiving a first allogeneic HCT and have demonstrated clinical engraftment at time of dosing
Meet one or more of the following criteria at the time of randomization:
Related (sibling) donor with at least one mismatch at one of these HLA-gene loci: HLA-A, -B or -DR
Haploidentical donor
Matched or Mismatched unrelated donor
Use of umbilical cord blood as stem cell source
Ex vivo graft manipulation resulting in T cell depletion
Received anti-thymocyte globulin or alemtuzumab (Campath-1H) Key
Exclusion Criteria
History of AdV, BKV, CMV, EBV, HHV-6, and/or JCV end-organ disease within 6 months prior to randomization
Evidence of active Grade >2 acute GVHD
Presence of non-minor uncontrolled or progressive bacterial, viral or fungal infections
Known history or current (suspected) diagnosis of Grade ≥3 CRS requiring treatment associated with the administration of peptides, proteins, and/or antibodies
Ongoing therapy with high-dose systemic corticosteroids (ie, prednisone equivalent dose >1.0 mg/kg/day) within 24 hours prior to dosing
Relapse of primary malignancy other than minimal residual disease Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05305040.
Locations matching your search criteria
United States
California
Palo Alto
Stanford Cancer Institute Palo Alto
Status: Active
Name Not Available
Ohio
Columbus
Nationwide Children's Hospital
Status: Active
Name Not Available
This is a Phase 2/3, multicenter, randomized, double-blind, placebo controlled trial
comparing posoleucel to placebo for the prevention of infection or disease due to AdV,
BKV, CMV, EBV, HHV-6, or JCV in high-risk adult and pediatric patients after allogeneic
HCT.
There are 2 parts to the study, a Phase 3 randomized study cohort described in this
posting, and an open label Phase 2 cohort described in NCT04693637, which has completed
enrollment. In this Phase 3 part, approximately 302 eligible allogeneic HCT recipients
will be enrolled and will receive 7 doses of posoleucel or placebo over 12 weeks,