Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ESHAP is a combination chemotherapy regimen used primarily as salvage therapy for relapsed or refractory lymphomas, including non-Hodgkin lymphoma, Hodgkin lymphoma, and sometimes myeloma. The acronym stands for its four components: - Etoposide (a topoisomerase II inhibitor) - Solu-Medrol (methylprednisolone; a glucocorticoid steroid) - High-dose Ara-C (cytarabine; an antimetabolite) - Cisplatin (a platinum-based alkylating agent) Etoposide, cytarabine, and cisplatin are cytotoxic agents that destroy rapidly dividing cells such as cancer cells. Methylprednisolone is a corticosteroid that suppresses immune response and can directly induce apoptosis in certain lymphoid malignancies. The regimen is typically administered intravenously over several days per cycle and may be used before autologous stem cell transplantation. ESHAP may also be combined with rituximab in some cases (R-ESHAP), but the canonical "ESHAP" does not include rituximab[1][2][3][5][6].
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 ESHAP.