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Clinical Trials/NCT01609036
NCT01609036
Terminated
Not Applicable

An Observational Phase IV Non Interventional Study in Patients With Advanced Follicular Lymphoma (III-IV) Evaluating the Safety of Maintenance Therapy With Rituximab After 8 Cycles of Rituximab in Combination With Chemotherapy as Induction Therapy in Previously Untreated Patients in Greece.

Hoffmann-La Roche0 sites3 target enrollmentOctober 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lymphoma, Follicular
Sponsor
Hoffmann-La Roche
Enrollment
3
Primary Endpoint
Safety: Incidence of adverse events
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

This observational study will evaluate the safety and efficacy of MabThera/Rituxan (rituximab) in previously untreated patients with follicular lymphoma. Data will be collected for 3 years

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
November 2012
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patients, \>/=18 years
  • Patients with previously untreated follicular lymphoma (stage III-IV) according to the approved summary of product characteristics (SPC)

Exclusion Criteria

  • Contraindications to MabThera/Rituxan therapy according to the approved SPC

Outcomes

Primary Outcomes

Safety: Incidence of adverse events

Time Frame: 3 years

Secondary Outcomes

  • Overall survival(3 years)
  • Event-free survival(3 years)
  • Progression-free survival(3 years)

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