Recruiting
Phase 1
Phase 2

Polatuzumab Vedotin (Pola) Plus Rituximab (R) in Patients With Post-transplant Lymphoproliferative Disorder (PTLD)

Sponsor:

Washington University School of Medicine

Code:

NCT06040320

Conditions

Post-transplant Lymphoproliferative Disorder

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Polatuzumab vedotin

Rituximab

CHP

Study Details

Eligibility Criteria

Study Design

Interventions and Outcome Measures

Central Contacts and Locations

More Information