Using bispecific antibodies in hematological malignancies is becoming widespread, with some of the bispecifics being approved in various diseases. We have conducted a number of studies using bispecifics in AML and AMG 330 was one of the earlier ones that was recently published. This was a Phase I dose escalation trial. We did see responses, but there was also some toxicity, including cytokine release syndrome and infusion reactions...
Using bispecific antibodies in hematological malignancies is becoming widespread, with some of the bispecifics being approved in various diseases. We have conducted a number of studies using bispecifics in AML and AMG 330 was one of the earlier ones that was recently published. This was a Phase I dose escalation trial. We did see responses, but there was also some toxicity, including cytokine release syndrome and infusion reactions. I think the target, which is CD33, is a viable target, although a more AML-specific target, if such a thing exists, will likely to be more beneficial in terms of the therapeutic window of such bispecific agents. And so perhaps we will have future bispecifics with higher potential. In terms of this agent, I’m not sure if this is going to go further in development