Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This high-dose combination chemotherapy regimen, followed by autologous progenitor cell transplantation (ASCT), was investigated by the National Cancer Institute (NCI) for the treatment of stage IIIB inflammatory breast cancer (IBC). The protocol involves an induction phase with paclitaxel and cyclophosphamide, followed by a consolidation phase using high-dose melphalan and etoposide. Paclitaxel acts as a microtubule stabilizer, preventing the disassembly of tubulin and arresting the cell cycle. Cyclophosphamide and melphalan are nitrogen mustard alkylating agents that form DNA cross-links, leading to cell death. Etoposide is a topoisomerase II inhibitor that induces double-stranded DNA breaks. Because the high-dose consolidation phase is severely myelosuppressive, autologous progenitor cells are reinfused to rescue and restore the patient's hematopoietic system.
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 paclitaxel + cyclophosphamide + melphalan + etoposide.