New antibody shows promise against Post-Transplant virus threat

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Underwent allogeneic hematopoietic stem cell transplantation (HSCT). 2. Documented EBV infection, defined as either: EBV DNAemia (EBV-DNA ≥400 copies/mL in plasma), or Pathologically confirmed EBV-associated lymphoproliferative disease with positive EBER by in situ hybridization. 3. Age ≥18 years, regardless of gender. 4. Negative for HIV, HBV, and HCV. 5. Eastern Cooperative Oncology Group Performance Status (ECOG-PS) score of 0-2. 6. Provision of signed informed consent prior to any study-related procedures. For patients aged 18 or above, consent must be provided by the patient themselves or an immediate family member. If obtaining consent directly from the patient is deemed medically detrimental to their condition, consent may be provided by a legal guardian or an immediate family member. Exclusion Criteria: * 1\. Presence of uncontrolled infection requiring mechanical ventilation or hemodynamic instability at the time of enrollment. 2\. Diagnosis of clinically significant severe hepatic insufficiency (defined as Child-Pugh Class C) within 5 days prior to enrollment. 3\. Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) levels exceeding 5 times the upper limit of normal (ULN), or serum total bilirubin exceeding 2 times ULN, within 5 days prior to enrollment. 4\. Diagnosis of end-stage renal dysfunction with a creatinine clearance rate of \<10 mL/min within 5 days prior to enrollment. 5\. Concurrent diagnosis of moderate hepatic insufficiency (defined as Child-Pugh Class B) and moderate renal dysfunction (defined as creatinine clearance rate \<50 mL/min). 6\. Cardiac function or disease meeting any of the following criteria: 1. Long QT syndrome or QTc interval \>480 ms. 2. Complete left bundle branch block, second-degree or third-degree atrioventricular block. 3. Severe, uncontrolled arrhythmia requiring pharmacological intervention. 4. New York Heart Association (NYHA) functional classification ≥ Class II. 5. Left ventricular ejection fraction (LVEF) \<50%. 6. History of myocardial infarction, unstable angina, severe unstable ventricular arrhythmia, or any other clinically significant arrhythmia requiring treatment within 6 months prior to enrollment; history of clinically significant pericardial disease; or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. 7\. Presence of uncontrolled severe acute graft-versus-host disease (aGVHD). 8. Evidence of active HIV replication prior to enrollment; detectable HCV antibody and HCV-RNA positivity within 90 days prior to enrollment; or HBsAg positivity. Known seropositivity for HIV or active hepatitis C virus. 9\. Presence of psychiatric disorders or other conditions that would compromise the patient's ability to comply with study treatment and monitoring requirements. 10\. Inability or unwillingness to provide written informed consent. 11. Patients deemed ineligible by the investigator due to other specific circumstances.