Reports Q3 revenue EUR2.0M vs. EUR14.9M last year. Anticipates our cash and cash equivalents will support operations into 2025. “We initiated our phase 2 clinical study of acimtamig in combination with AlloNK(R) and received encouraging feedback on the design of our LuminICE-203 trial from the FDA,” said Dr. Adi Hoess, CEO of Affimed. “We also continued to make progress with AFM24 in combination with atezolizumab and advanced AFM28 in the dose escalation. This positions our company well to report further updates on all three clinical programs within the next few months.”
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