Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Lomustine + etoposide + cyclophosphamide (LEC)** is an oral or intravenous combination chemotherapy regimen consisting of three alkylating and cytotoxic agents: lomustine (a nitrosourea alkylating agent), etoposide (a topoisomerase II inhibitor), and cyclophosphamide (a nitrogen mustard alkylating agent). It is primarily used as a second- or third-line treatment for relapsed small cell lung cancer (SCLC) and as a conditioning regimen for autologous hematopoietic stem cell transplantation (ASCT) in relapsed Hodgkin's and non-Hodgkin's lymphomas, often as an alternative to carmustine-based regimens like CBV due to drug shortages. Clinical studies report response rates of approximately 38% in SCLC, median survival of 4.4 months, and favorable 2-year overall survival (85%) in lymphoma ASCT settings with acceptable toxicity, though hematological adverse events and rare treatment-related mortality occur.[1][2][3]
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 lomustine + etoposide + cyclophosphamide.