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An Observational Study of MabThera/Rituxan (Rituximab) in Patients With Follicular Lymphoma

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Roche

Status

Terminated

Conditions

Lymphoma, Follicular

Study type

Observational

Funder types

Industry

Identifiers

NCT01609036
ML22236

Details and patient eligibility

About

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

Enrollment

3 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

3 participants in 1 patient group

Cohort

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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