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Trial information

A Study of MabThera (Rituximab) as Maintenance Therapy in Patients With Aggressive Non-Hodgkin's Lymphoma

Status: Recruiting

Protocol number: ML18223

Sponsor: Roche Austria GmbH

Company division: Pharmaceutical

Official Scientific Title: A randomized, open-label study of MabThera as maintenance therapy compared with treatment-free observation on event-free survival in patients with aggressive B-cell non-Hodgkin's lymphoma

Brief summary: This study will evaluate the efficacy and safety of maintenance therapy with MabThera compared with observation (ie no treatment) in patients with aggressive B-cell non-Hodgkin`s lymphoma who had a complete response following first-line treatment with MabThera plus a chemotherapy regimen. The anticipated time on study treatment is 3-12 months, and the target sample size is 100-500 individuals. Target sample size is 600.

Study phase: IV

Study type: Interventional; Treatment; Non-Randomized; Open Label; Uncontrolled; Parallel; Safety/Efficacy study

Condition: Non-Hodgkin's Lymphoma

Intervention type: Drug

Intervention name: rituximab[MabThera/Rituxan]

Primary outcome: 1. Clinical efficacy as measured by event-free survival

Key secondary outcomes: 1. Quality of life, evolution of immunocompetence, safety, and overall survival

Inclusion criteria:

  • adult patients >=18 years of age;
  • aggressive B-cell non-Hodgkin's lymphoma;
  • treatment benefit from prior MabThera plus chemotherapy.

Exclusion criteria:

  • first-line NHL therapy other than specified in the inclusion criteria;
  • more than one prior chemo- or chemoimmunotherapy regimen;
  • history of malignancy other than squamous cell cancer, basal cell cancer of the skin, or in situ cancer of the cervix within the last 5 years;
  • active opportunistic infections.

Gender: Males or Females

Age limits: Min: 18 Years Max: N/A (No limit)

Accepts healthy volunteers: No

Anticipated start date: May, 2004

Trial registration date: 08/29/2005

Date last updated: 11/21/2008


Link to trial result

This trial is being conducted at the following locations:

Argentina

  • Buenos Aires
  • La Plata

Australia

  • Gosford
  • Greenslopes
  • Hobart
  • Sydney
  • Wodonga

Austria

  • Bludesch
  • Bregenz
  • Dornbirn
  • Fürstenfeld
  • Graz
  • Hall In Tirol
  • Hohenems
  • Innsbruck
  • Klagenfurt
  • Kufstein
  • Leoben
  • Linz
  • Oberpullendorf
  • Oberwart
  • Ried-Innkreis
  • Salzburg
  • St Pölten
  • Steyr
  • Villach
  • Vöcklabruck
  • Waidhofen A D Thaya
  • Wels
  • Wien
  • Wiener Neustadt
  • Zams

Bosnia and Herzegovina

  • Banja Luka
  • Kasindo
  • Sarajevo
  • Tuzla

Brazil

  • Campinas
  • Goiania
  • Salvador
  • Sao Paulo

Bulgaria

  • Pleven
  • Plovdiv
  • Sofia
  • Varna

China

  • Beijing
  • Chengdu
  • Guangzhou
  • Haerbin
  • Hong Kong
  • Jiangsu
  • Shanghai

Croatia

  • Zagreb

Czech Republic

  • Brno
  • Hradec Kralove
  • Ostrava
  • Praha

Estonia

  • Tallinn
  • Tartu

Israel

  • Afula
  • Beer Sheva
  • Haifa
  • Jerusalem
  • Kfar Saba
  • Petah Tikva
  • Ramat Gan
  • Rehovot
  • Tel Aviv

Latvia

  • Riga

Macedonia, The Former Yugoslav Republic of

  • Skopje

Malaysia

  • Kuala Lumpur

Mexico

  • Leon
  • Mexico City
  • Monterrey
  • Puebla

Peru

  • Arequipa
  • Callao

Romania

  • Brasov
  • Bucharest
  • Iasi
  • Targu-Mures

Russian Federation

  • Belgorod
  • Chelyabinsk
  • Ekaterinburg
  • Irkutsk
  • Kazan
  • Kirov
  • Korolev
  • Moscow
  • Nizhny Novgorod
  • Novosibirsk
  • Rostov-Na-Donu
  • Saint-Petersburg
  • St Petersburg
  • Stavropol
  • Surgut
  • Tumen
  • Ufa
  • Ulyanovsk
  • Volgograd
  • Yaroslavl

Slovakia

  • Bratislava
  • Kosice
  • Martin

Slovenia

  • Ljubljana

South Africa

  • Pietermaritzburg
  • Pretoria

Sweden

  • Falun
  • Lulea
  • Stockholm
  • Sundsvall
  • Uddevalla

Taiwan

  • Kaohsiung
  • Taichung
  • Taipei

Thailand

  • Bangkok
  • Chiang Mai
  • Khon Kaen
  • Songkhla

Turkey

  • Ankara
  • Aydin
  • Eskisehir
  • Gaziantep
  • Kayseri

To contact Roche for more information on this trial please complete the email form below. Treatment decisions and/or suitability for a specific trial are decisions only your healthcare provider can make. If you are patient interested in any of the studies, please have your healthcare provider contact us via this website, and they will be provided with the relevant clinical trial information.

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