Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Bendamustine + gemcitabine + vinorelbine (BeGEV)** is a combination chemotherapy regimen used as salvage induction therapy prior to autologous stem-cell transplantation (ASCT) in patients with relapsed or refractory Hodgkin lymphoma (HL) after one prior line of chemotherapy. It consists of bendamustine (90 mg/m² IV on days 2-3), gemcitabine (800 mg/m² IV on days 1 and 4), vinorelbine (20 mg/m² IV on day 1), and prednisolone (100 mg PO on days 1-4), administered every 21 days for four cycles in an outpatient setting. In a multicenter phase II trial (NCT01884441), it achieved a 73% complete response rate and 83% overall response rate in 59 patients, with successful stem-cell mobilization in 96% of evaluable cases and favorable 2-year PFS of 62% overall (81% post-ASCT). Common grade 3-4 toxicities included neutropenia (14%), thrombocytopenia (14%), febrile neutropenia (12%), and infection (7%), with high dose intensity (>98%) maintained.[1][2][4]
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 bendamustine + gemcitabine + vinorelbine.