A Single Arm, Multicentre, Phase IIIB Study to Evaluate Safety, Efficacy and Pharmacokinetic (PK) of Subcutaneous (SC) Rituximab Administered During Induction Phase or Maintenance in Previously Untreated Patients With CD20+ Diffuse Large B Cell Lymphoma (DLBCL) or Follicular Lymphoma (FL)

Trial Profile

A Single Arm, Multicentre, Phase IIIB Study to Evaluate Safety, Efficacy and Pharmacokinetic (PK) of Subcutaneous (SC) Rituximab Administered During Induction Phase or Maintenance in Previously Untreated Patients With CD20+ Diffuse Large B Cell Lymphoma (DLBCL) or Follicular Lymphoma (FL)

Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 29 Jun 2017

At a glance

  • Drugs Rituximab (Primary)
  • Indications Diffuse large B cell lymphoma; Follicular lymphoma
  • Focus Adverse reactions
  • Acronyms MABRELLA
  • Sponsors Roche
  • Most Recent Events

    • 25 Jun 2017 Results of safety analysis (n=421) from MabRella study (NCT01889069; NCT01987505; NCT02406092), presented at the 22nd Congress of the European Haematology Association.
    • 06 Dec 2016 Pooled interim analysis data of this trial and two other trials (NCT01987505 and NCT02406092) presenting safety data were presented at the 58th Annual Meeting and Exposition of the American Society of Hematology.
    • 23 Dec 2014 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov record.
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