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First patient dosed in Phase 1 Trial
Iksuda announces first patient dosed in Phase 1 trial of IKS014


Iksuda Therapeutics receives FDA IND clearance for IKS014
FDA decision will enable Iksuda to expand its ongoing clinical trial in the US, Australia and Singapore. Preliminary data from an ongoing dose-escalation study of IKS014 has shown meaningful clinical activity across multiple tumour types
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