BelaCarD Study (AMaRC 19-02)
This is a phase I/II open label single arm clinical study. Patients with Relapsed/Refractory Multiple Myeloma who have had 1 to 3 prior lines of treatment, will receive Belantamab Mafodotin in combination with carfilzomib and dexamethasone. (BelaCarD)
There will be two phases in the study. The first, safety, run-in phase will consist of 10 patients. After the 10th evaluable patient has completed the 1st cycle, the trial management committee (TMC) will hold a meeting to assess whether or not there are any safety concerns at that dosing schedule. Provided that no more than 4 patients experience a grade 4, treatment-emergent toxicity, and subject to the confirmatory advice from the Data Safety and Monitoring Committee (DSMC), the expansion phase will commence at the same treatment dose and schedule.
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Australasian Myeloma Research Consortium (AMaRC C/- Alfred Health)
Other (specify below)
Can this be done remotely?
Parts of research done:
Addition of sites for study recruitment
Prospective researchers receive: