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Clinical Trial Summary

Phase II Gemcitabine + HD Chemotherapy Followed by PBSC Rescue for HD


Clinical Trial Description

To assess the non-hematologic toxicity and determine the phase II dose of gemcitabine in combination with vinorelbine followed by carmustine, etoposide and cyclophosphamide and autologous hematopoietic stem cell transplantation. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00388349
Study type Interventional
Source Stanford University
Contact
Status Completed
Phase Phase 2
Start date September 2001
Completion date September 2010

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