Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Rituximab + ifosfamide + carboplatin + etoposide (VP-16) + mesna + G-CSF is a dose-escalated chemoimmunotherapy regimen, often referred to as R-ICEesc or augmented R-ICE. Developed by Memorial Sloan Kettering Cancer Center, it is primarily used as a second-line salvage therapy for patients with primary refractory or relapsed aggressive B-cell non-Hodgkin lymphomas (NHL), such as diffuse large B-cell lymphoma (DLBCL), prior to autologous stem cell transplantation (ASCT). The regimen combines the anti-CD20 monoclonal antibody rituximab with the ICE chemotherapy backbone (ifosfamide, carboplatin, and etoposide). Mesna is included as a uroprotective agent to mitigate ifosfamide-induced hemorrhagic cystitis, and G-CSF is administered to support bone marrow recovery and facilitate peripheral blood progenitor cell mobilization.
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 rituximab + ifosfamide + carboplatin + etoposide + mesna + filgrastim.