About this trial
This is a Phase I/II, modular, open-label, multicenter, dose escalation, and dose expansion/optimization study to evaluate the safety, tolerability, PK, immunogenicity, pharmacodynamics and efficacy of AZD0305 as monotherapy and in combination with other anticancer agents in participants with MM.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Participants must be at least 18 years of age or the legal age of consent in the jurisdiction
in which the study is taking place;
Eastern Cooperative Oncology Group performance status of ≤ 2 in module 1, or 0 or 1 in modules 2 and 3;
Documentation of Multiple Myeloma (MM) as defined by International Myeloma Working Group (IMWG) Diagnostic Criteria for Multiple Myeloma. Site should ensure that Multiple Myeloma diagnosis is confirmed in accordance with the IMWG Diagnostic Criteria;
Disqualifiers
Amyloidosis, plasma cell leukemia, Waldenstrom Macroglobulinemia, Polyneuropathy Organomegaly Endocrinopathy M-protein and Skin Syndrome, or Smoldering Multiple Myeloma (compliant with WHO criteria);
Participants exhibiting clinical signs of central nervous system involvement of MM;
Participants with known COPD, or previous history of ILD/pneumonitis;
Participants with known moderate or severe persistent asthma within the past 5 years, or uncontrolled asthma of any classification;
Trial design
Sequential
Treatments tested in this trial
AZD0305
DrugAZD0305 Investigational product
Elranatamab
DrugModule 2 Investigational product
Pomalidomide
DrugModule 3 Standard of Care (background treatment)
Dexamethasone
DrugModule 3 Standard of Care (background treatment)
Treatment groups
Trial outcomes
Primary outcomes
Occurrence of dose-limiting toxicity (DLT), as defined in the protocol (Phase Ia dose escalation only)
A DLT is any toxicity occuring from the first dose of AZD0305 up to and including the planned end of Cycle 1 (the DLT assessment period) that is assessed as unrelated to the disease or disease-related processes under investigation and which includes, any death not clearly due to the underlying disease or extraneous causes, pre-defined haematological and non-haematological toxicities
Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Number of patients with adverse events and serious adverse events by system organ class and preferred term
Frequency of dose modifications, dose delays, and treatment discontinuations due to AEs (Module 2 and Module 3)
Number and percentage of participants with dose modifications, dose delays, and permanent discontinuations due to adverse events (for AZD0305 and combination agent\[s\], as applicable), per protocol-defined dose modification rules.
Secondary outcomes
Phase Ia: Objective Response Rate (ORR)
The percentage of patients with a confirmed investigator assessed sCR, CR, VGPR or PR according to IMWG criteria
Phase Ia: Duration of response (DoR)
The time from the date of first response until date of disease progression or death in the absence of disease progression
Phase Ia: Progression free Survival (PFS)
The time from first dose until IMWG defined disease progression or death
Phase Ia: Overall Survival (OS)
The time from the date of the first dose of study treatment until death due to any cause
Sponsors and contacts
Click on the lead sponsor to view all of their trials.