AERN Abskopaler Effekt von Radiotherapie und Nivolumab bei anti-PD1 vorbehandeltem rezidiviertem oder refraktärem Hodgkin-Lymphom (HL) (Aktiv)
ASTRAL ASTRAL- a Clinical Study to Assess the Efficacy and Toxicity of High-dose Chemotherapy (Aktiv)
BMS CA 209-744 The purpose of this study is to determine whether nivolumab plus brentuximab vedotin (followed by brentuximab vedotin plus bendamustine in patient with suboptimal response) is safe and effective in treating patients with Hodgkin's lymphoma (cHL). Eligible patients are children, adolescents, and young adults relapsed or refractory to first line. (Aktiv)
CC-220-NHL-001 A Phase 1/2, Multicenter, Open-Label Study to Assess Safety, Pharmacokinetics, and preliminary efficacy of CC-220, alone and in combination with an anti-CD20 Monoclonal Antibody (MAB) in subjects with relapsed or refractory Lymphomas (Aktiv)
GC-LTFU-001 Long-Term Follow-up Protocol for Participants Treated With Gene-Modified T Cells (Aktiv)
HD 21 Treatment optimization Trial in the first-line Treatment of advanced stage Hodgin-Lymphoma (Aktiv)
MK7684A-004 Phase II Studie zu MK-7684A (Vibostolimab/Pembrolizumab) bei rezidivierenden/refraktären hämatologischen Krebserkrankungen (Aktiv)