A Study to Evaluate the Safety and Tolerability of RO7296682 in Participants With Advanced Solid Tumors.

A Study to Evaluate the Safety and Tolerability of RO7296682 in Participants With Advanced Solid Tumors

  • Cancer
  • Solid Tumors
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:

Terminated

This trial runs in
Countries
  • Australia
  • Belgium
  • Canada
  • Denmark
  • Spain
Trial Identifier:

NCT04158583 2019-002830-35 WP41188

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Trial Summary

      This study was planned to evaluate the safety and tolerability of RO7296682 in participants with advanced solid tumors.

      Hoffmann-La Roche Sponsor
      Phase 1 Phase
      NCT04158583, WP41188, 2019-002830-35 Trial Identifier
      RO7296682 Treatments
      Solid Tumors Condition
      Official Title

      An Open-Label, Multicenter Phase 1 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO7296682, A CD25-Targeting, T-Regulatory Cell Depleting Antibody in Participants With Advanced and/or Metastatic Solid Tumor

      Eligibility Criteria

      All Gender
      ≥18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Diagnosis of advanced and/or metastatic solid tumors who have progressed on all standard therapies, are intolerant to Standard-Of-Care (SOC), and/or are non-amenable to SOC. Participants whose tumors have known sensitizing mutation must have experienced disease progression (during or after treatment) or intolerance to treatment with a respective targeted therapy.
      • Measurable disease according to response evaluation criteria in solid tumors (RECIST) v1.1.
      • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
      • Able to provide the most recent archival tumor tissue samples.
      • Adequate cardiovascular, haematological, liver and renal function.
      • Participants on therapeutic anticoagulation must be on a stable anticoagulant regimen.
      • Women of Childbearing Potential: Agreement to remain abstinent (refrain from heterosexual intercourse) or use highly effective contraceptive methods.
      • Men: Agreement to remain abstinent (refrain from heterosexual intercourse) or use highly effective contraceptive methods and refrain from donating sperm.
      Exclusion Criteria
      • Pregnancy, lactation, or breastfeeding.
      • Known hypersensitivity to any of the components of RO7296682, including but not limited to hypersensitivity to Chinese hamster ovary cell products or other recombinant human or humanized antibodies.
      • History or clinical evidence of central nervous system (CNS) primary tumors or metastases.
      • Participants with another invasive malignancy in the last two years.
      • Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results.
      • Participants with known active or uncontrolled infection.
      • Positive human immunodeficiency virus (HIV) test at screening.
      • Positive for Hepatitis B and C.
      • Vaccination with live vaccines within 28 days prior to C1D1.
      • Major surgical procedure or significant traumatic injury within 28 days prior to first RO7296682 infusion.
      • Participants with wound healing complications.
      • Dementia or altered mental status that would prohibit informed consent.
      • History of Stevens-Johnson syndrome, toxic epidermal necrolysis, or DRESS (drug rash with eosinophilia and systemic symptoms).
      • Active or history of autoimmune disease or immune deficiency.
      • Prior treatment with checkpoint inhibitors (CPIs) (e.g. anti-CTLA4, anti-PD1, anti-PDL1), immunomodulatory monoclonal antibodies (mAbs) and/or mAb-derived therapies (approved or investigational) is approved.
      • Prior treatment with a CC chemokine receptor 4 (CCR4)-targeting (e.g. mogamulizumab) or a CD25-targeting agent (e.g. basiliximab) is prohibited.
      • Treatment with standard radiotherapy, any chemotherapeutic agent, targeted therapy or treatment with any other investigational drug (defined as treatment for which there is currently no regulatory authority-approved indication) within 28 days or 5 half-lives of the drug (whichever is shorter), prior to the first RO7296882 administration on C1D1.
      • Radiotherapy within the last 4 weeks before start of study drug treatment, with the exception of limited palliative radiotherapy (for which no wash out period is required).

      For the latest version of this information please go to www.forpatients.roche.com

       

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