A Study Evaluating the Safety and Efficacy of Multiple Treatments in Participants With Multiple Myeloma

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorHoffmann-La Roche

About this trial

CO43923 is a platform study that will evaluate the safety, efficacy, and pharmacokinetics (PK) of multiple treatment combinations, as monotherapy or in combination, in participants with multiple myeloma (MM). The study is designed with the flexibility to open new treatment substudies as new treatments become available. Information regarding the opened substudies are found below.

Eligibility criteria

Qualifiers

Diagnosed with MM per International Myeloma Working Group (IMWG) criteria

Eastern Cooperative Oncology Group Performance Status of 0, or 1, or 2

Resolution of AEs from prior anti-cancer therapy to Grade <=1

Agreement to undergo scheduled assessments and procedures

Disqualifiers

Inability to comply with protocol-mandated hospitalization and procedures

History of confirmed progressive multifocal leukoencephalopathy

History of other malignancy within 2 years prior to screening

Current or past history of central nervous system (CNS) disease

Trial design

Treatments tested in this trial

  • Cevostamab
  • Lenalidomide
  • Tocilizumab
  • Iberdomide
  • Dexamethasone

Treatment groups

200 Participants
are divided into 2 treatment groups

Locations

16
Australia
Prince of Wales Hospital2031, RandwickNew South Wales, Australia
St Vincent's Hospital Melbourne3065, FitzroyVictoria, Australia
France
CHU Lyon Sud - Service Hématologie69310, Pierre-Bénite France
IUCT Oncopole31059, Toulouse France

Sponsors and collaborators

Hoffmann-La Roche

Lead sponsor