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An open-label, multi-centre, dose escalating, phase I/randomized phase II study to investigate the safety and tolerability of RO5072759 given as monotherapy in patients with CD20+ malignant disease

Mise à jour : Il y a 4 ans
Référence : EUCTR2008-003460-19

Femme et Homme

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Extrait

To investigate the overall response rate and safety data of RO5072759 (1000mg flat dose) given as monotherapy in patients with relapsed CD20+ indolent NHL compared with rituximab(375mg/m2) monotherapy.

Critère d'inclusion

  • Patients with CD20+ Non-Hodgkin’s Lymphoma and Leukemia

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