Ohio Gov. Mike DeWine stopped by Cincinnati Children’s on Dec. 5 to announce a major boost for pediatric cancer research—a $1.48 million grant to power the ENGRAFT learning network. This collaborative effort brings together experts, families, and partners to transform outcomes for kids needing stem cell transplants, as part of a $5 million statewide investment in fighting childhood cancer.
The new Applied Gene and Cell Therapy Center will expand capacity for manufacturing viral vectors and cell-based products under Current Good Manufacturing Practice conditions, supporting complex trials in oncology, hematology and rare genetic disorders, with capabilities for large-scale bioreactor production and post-approval therapy manufacturing.
Cincinnati Children’s surgeons use advanced minimally invasive, fluorescence-guided, robotic and HIPEC techniques to improve outcomes for complex pediatric tumors.
A Phase II clinical trial conducted in Ghana suggests that hydroxyurea — already a treatment offered for the most common form of sickle cell disease — also shows benefits for those with the hemoglobin SC (HbSC) variant of the condition.
Discover how Cincinnati Children’s is accelerating research and clinical trials to advance therapies for myeloid malignancies across all age groups.
ENGRAFT, a new learning health network led by Cincinnati Children’s, brings together pediatric and adult centers to improve transplant and cellular therapy outcomes.
Meet the experts joining the Cancer and Blood Diseases Institute to advance care and research in pediatric oncology, hematology, bone marrow transplantation and proton therapy.
Specialists in oncology, hematology, bone marrow transplantation and proton therapy join the Cancer and Blood Diseases Institute to enhance precision medicine and multidisciplinary care.
Cincinnati Children’s unveils advanced genomic tools for pediatric cancer care—CinCSeq and Histiotrak offer faster, more precise diagnostics and monitoring.
A look at how Cincinnati Children’s is advancing care for relapsed T-ALL and T-LBL through a novel CAR T‑cell therapy, offering new hope for resistant disease.