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Clinical Trial Summary

This is a multi-site phase 1 study of the safety, immunologic and virologic responses of ex vivo expanded donor-derived (DD) HIV-1 multi-antigen specific T-cell (HST) with non-escaped epitope targeting (NEET) therapy as a therapeutic strategy in HIV-infected individuals following Allogeneic Bone Marrow Transplantation (alloBMT).


Clinical Trial Description

The primary objective of this study is to evaluate the safety of donor-derived allogeneic expanded HIV-specific T-cell therapy (DD HST-NEETs) in HIV-infected alloBMT recipients on ART. Eligible donors will undergo a blood draw of up to 300mL to allow production of allogeneic DD HST-NEETs. Participants who meet specified inclusion criteria including neutrophil recovery post-transplant and for whom donor products have passed release testing will receive DD HST-NEETs at a dose of 2x107/m2 within 30 days of screening visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04248192
Study type Interventional
Source Children's National Research Institute
Contact Richard Ambinder, MD, PhD
Phone 410 955-8839
Email rambind1@jhmi.edu
Status Recruiting
Phase Phase 1
Start date May 1, 2020
Completion date April 2025