Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CEEP + rituximab is a high-dose chemoimmunotherapy regimen consisting of the chemotherapy combination CEEP (cyclophosphamide, epirubicin, etoposide, and prednisone) administered alongside the anti-CD20 monoclonal antibody rituximab. This regimen is primarily utilized as a high-dose conditioning therapy followed by autologous stem cell transplantation (ASCT) for patients with diffuse large B-cell lymphoma (DLBCL). Rituximab targets the CD20 antigen on B-lymphocytes, inducing cell death through antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). The chemotherapy components provide synergistic cytotoxic effects: cyclophosphamide acts as a DNA alkylating agent; epirubicin and etoposide inhibit DNA topoisomerase II, leading to DNA strand breaks and apoptosis; and prednisone serves as a lympholytic corticosteroid. This specific protocol was evaluated in clinical trials led by Nantes University Hospital and the GOELAMS group to compare high-dose therapy against standard CHOP-14 plus rituximab in frontline settings for high-risk DLBCL patients.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on CEEP + rituximab.