A Study Evaluating the Safety and Pharmacokinetics of Escalating Doses of RO7425781 in Participants With Relapsed or Refractory Multiple Myeloma (r/r MM)

  • Multiple Myeloma
Trial Status:

Recruiting

This trial runs in
Cities
  • cascina-perseghetto
  • London
  • Milano
  • Nantes
  • Santander
Trial Identifier:

NCT04557150 2020-002012-46 BP42233

      Show trial locations

      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.

      Results Disclaimer

      Trial Summary

      This is a first-in-human, open-label, uncontrolled, multi-center, monotherapy, dose-escalation and dose expansion study. RO7425781 will be administered to participants with r/r MM for whom no standard-of-care treatment exists or who are intolerant to those established therapies. The study consists of two parts: dose-escalation of RO7425781 (Part 1) and a randomized dose expansion of RO7425781 (Part 2).

      Hoffmann-La Roche Sponsor
      Phase 1 Phase
      NCT04557150 , BP42233 , 2020-002012-46 Trial Identifier
      RO7425781 Treatments
      Multiple Myeloma Condition
      Official Title

      An Open-Label, Multicenter, Phase I Study Evaluating the Safety and Pharmacokinetics of Escalating Doses of RO7425781 in Participants With Relapsed or Refractory Multiple Myeloma

      Eligibility Criteria

      All Gender
      ≥18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Previously diagnosed with Multiple Myeloma (MM) based on standard criteria.
      • Dose Escalation Phase and Dose Expansion Phase: Participants with r/r MM who have previously received therapy with an Immunomodulatory drug (IMiD) and Proteasome Inhibitor (PI) and are intolerant to or have no other option for standard-of-care treatment according to the Investigator.
      • Life expectancy of at least 12 weeks.
      • Agreement to provide protocol-specific biopsy material.
      • AEs from prior anti-cancer therapy resolved to Grade =<1.
      • Measurable disease.
      • For female participants of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse), use contraceptive measures and refrain from donating eggs.
      • For male participants: agreement to remain abstinent (refrain from heterosexual intercourse), use contraceptive measures and refrain from donating sperm.
      Exclusion Criteria
      • Inability to comply with protocol-mandated hospitalization and activities restrictions.
      • Pregnant or breastfeeding, or intending to become pregnant during the study or within 3 months after the last dose of study drug.
      • Prior use of any monoclonal antibody, radioimmunoconjugate, or antibody-drug conjugate for MM treatment within 2 weeks before first RO7425781 administration.
      • Prior treatment with systemic immunotherapeutic agents within 2 weeks before first RO7425781 administration.
      • Treatment-related, immune-mediated AEs associated with prior immunotherapeutic agents.
      • Treatment with radiotherapy, any chemotherapeutic agent, or treatment with any other anti-cancer agent (investigational or otherwise) within 2 weeks, prior to first RO7425781 administration. Limited field palliative radiotherapy for bone pain or for soft tissue lesions is allowed.
      • Autologous or allogeneic stem cell transplantation (SCT) within 100 days prior to first RO7425781 infusion and/or signs of chronic graft versus host disease or ongoing immunosuppressive medication.
      • Prior solid organ transplantation.
      • Active auto-immune disease or flare within 6 months prior to start of study treatment
      • Any medical condition or abnormality in clinical laboratory tests that, in the Investigator's or Medical Monitor's judgment, precludes the participant's safe participation in and completion of the study, or which could affect compliance with the protocol or interpretation of results.

      About Clinical Research

      What is a clinical trial? Why should I consider taking part in a clinical trial? And why does Genentech conduct clinical trials?

      Find out now