Condition: Solid Tumor · Sponsor: Children's National Research Institute
This is a phase I dose-escalation study to evaluate the safety of partially human leukocyte antigen (HLA)-matched multi tumor-associated antigen-specific T cell (TAA-T) therapy for patients with high-risk solid tumors due to the presence of refractory, relapsed and/or minimal residual detectable disease following conventional therapy. Conventional therapy may include chemotherapy, surgery, radiation, autologous stem cell transplant, or targeted therapy.
This description comes directly from the study's public registry record.
Amy Hont, MD · 202-476-3887 · ahoughte@childrensnational.org
Fahmida Hoq, MBBS · 202-476-3634 · fhoq@childrensnational.org
Always discuss trial participation with your own doctor first.
| Children's National Hospital | Washington D.C., District of Columbia, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05238792