A Study Evaluating the Safety and Efficacy of Atezolizumab in Combination With Obinutuzumab Plus Lenalidomide in Patients With Relapsed or Refractory Follicular Lymphoma

  • Follicular Lymphoma
Trial Status:

Completed

This trial runs in
Cities
  • Birmingham
  • Charlotte
  • Créteil
  • Dijon
  • Le Mans
  • Lille
  • Louisville
  • Miami
  • Montpellier
  • Nantes
  • New York
  • Pierre-Bénite
  • Rennes
  • Rouen
  • Toulouse
Trial Identifier:

NCT02631577 2015-002467-42 BO29562

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      The source of the below information is the publicly available website ClinicalTrials.gov. It has been summarised and edited into simpler language.

      The below information is taken directly from the publicly available website ClinicalTrials.gov within a week of any updates, and has not been edited.

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      Trial Summary

      This study will evaluate the safety, efficacy, pharmacokinetics and immunogenicity of induction treatment consisting of atezolizumab in combination with obinutuzumab plus lenalidomide in patients with relapsed or refractory follicular lymphoma (FL), followed by maintenance treatment with atezolizumab plus obinutzumab plus lenalidomide in patients who achieve a complete response (CR), a partial response (PR), or stable disease at end of induction.

      Hoffmann-La Roche Sponsor
      Phase 1/Phase 2 Phase
      NCT02631577 , BO29562 , 2015-002467-42 Trial Identifier
      Atezolizumab (MPDL3280A) [TECENTRIQ], Lenalidomide, Obinutuzumab Treatments
      Lymphoma, Follicular Condition
      Official Title

      A Phase Ib/II Study Evaluating the Safety and Efficacy of Atezolizumab in Combination With Obinutuzumab Plus Lenalidomide in Patients With Relapsed or Refractory Follicular Lymphoma

      Eligibility Criteria

      All Gender
      ≥18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2
      • Relapsed or refractory FL after treatment with at least one prior chemoimmunotherapy regimen that included an anti-CD20 monoclonal antibody and for which no other more appropriate treatment option exists as determined by the investigator
      • Histologically documented CD20-positive lymphoma as determined by the local laboratory
      • Fluorodeoxyglucose-avid lymphoma (i.e., PET-positive lymphoma)
      • At least one bi-dimensionally measurable lesion (>1.5 cm in its largest dimension by CT scan or magnetic resonance imaging [MRI])
      • Availability of a representative tumor specimen and the corresponding pathology report for retrospective central confirmation of the diagnosis of FL
      • Agreement to comply with all local requirements of the lenalidomide risk minimization plan
      • For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use two adequate methods of contraception, including at least one method with a failure rate of <1% per year, for at least 28 days prior to Day 1 of Cycle 1, during the treatment period (including periods of treatment interruption), and for at least 18 months after the last dose of study treatment
      • For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures and agreement to refrain from donating sperm for at least 3 months after the last dose of study treatment
      Exclusion Criteria
      • Grade 3b follicular lymphoma
      • History of transformation of indolent disease to diffuse large B-cell lymphoma (DLBCL)
      • Known CD20-negative status at relapse or progression
      • Central nervous system lymphoma or leptomeningeal infiltration
      • Prior allogeneic stem-cell transplantation (SCT)
      • Completion of autologous SCT within 100 days prior to Day (D) 1 of Cycle (C) 1
      • Prior standard or investigational anti-cancer therapy as specified in protocol
      • History of resistance to lenalidomide or response duration of <1 year
      • Treatment with systemic immunosuppressive medications
      • History of solid organ transplantation
      • Clinically significant toxicity from prior therapy that has not resolved to Grade <=2 (according to the National Cancer Institute Common Terminology Criteria for Adverse Events [NCI CTCAE], v4.0) prior to Day 1 of Cycle 1
      • History of erythema multiforme, Grade >= 3 rash, or blistering following prior treatment with immunomodulatory derivatives such as thalidomide and lenalidomide
      • Active bacterial, viral, fungal, or other infection
      • Positive for hepatitis B surface antigen (HBsAg), total hepatitis B core antibody (HBcAb), or hepatitis C virus (HCV) antibody at screening
      • Known history of HIV positive status
      • History of progressive multifocal leukoencephalopathy
      • History of autoimmune disease
      • Contraindication to treatment for TE prophylaxis
      • Grade <= 2 neuropathy
      • History of other malignancy that could affect compliance with the protocol or interpretation of results
      • Evidence of any significant, uncontrolled concomitant disease
      • Inadequate hematologic function (unless due to underlying lymphoma)
      • Abnormal laboratory values (unless due to underlying lymphoma)
      • Pregnant or lactating or intending to become pregnant during the study

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