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An Observational Study of MabThera/Rituxan (Rituximab) Plus Chemotherapy As First-Line Treatment in Patients With Diffuse Large B-Cell Lymphoma or Follicular Lymphoma

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Roche

Status

Completed

Conditions

Diffuse Large B-Cell Lymphoma

Study type

Observational

Funder types

Industry

Identifiers

NCT01340443
ML25435

Details and patient eligibility

About

This observational study will evaluate the safety and efficacy of MabThera/Rituxan (rituximab) plus chemotherapy as first-line treatment in patients with diffuse large B-cell lymphoma (DLBCL) or follicular lymphoma (FL). Data will be collected from each patient during the 6 months of induction treatment and for up to 3 years of follow-up.

Enrollment

314 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histologically confirmed CD20+ diffuse large B-cell lymphoma or follicular lymphoma
  • Treatment with MabThera/Rituxan as per locally approved China package insert
  • Documented patient with medical records

Exclusion criteria

  • Previous treatment for diffuse large B-cell lymphoma or follicular lymphoma

Trial design

314 participants in 1 patient group

Cohort

Trial contacts and locations

24

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Data sourced from clinicaltrials.gov

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