A Study to Evaluate RO7851624 in Participants With Relapsed/Refractory Multiple Myeloma (RRMM)

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorGenentech, Inc.

About this trial

This study will evaluate safety, pharmacokinetics (PK), clinical activity and pharmacodynamics (PD) of RO7851624 in participants with RRMM who are triple-class exposed (treated with proteasome inhibitors \[PIs\], immunomodulators \[IMiDs\], and anti-cluster of differentiation 38 \[anti-CD38\] monoclonal antibodies), and have limited remaining standard treatment options due to refractoriness, intolerance, or multiple prior therapies.

Eligibility criteria

Qualifiers

Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.

Life expectancy of at least 12 weeks.

Diagnosis of multiple myeloma per International Myeloma Working Group (IMWG) criteria.

Measurable disease.

Disqualifiers

Treatment with any chemotherapeutic agent, or treatment with any other anti-cancer agent (investigational or otherwise) with insufficient washout prior to first dose of study treatment.

Autologous stem cell transplant (SCT) with insufficient time prior to first dose of study treatment.

Prior allogeneic SCT.

Prior solid organ transplantation.

Trial design

Treatments tested in this trial

  • RO7851624

Treatment groups

160 Participants
are divided into 1 treatment group

Sponsors and collaborators