Ikena Oncology gets FDA fast track designation for IK-930 in mesothelioma
Ikena Oncology has secured fast track designation for IK-930 from the US Food and Drug Administration in the treatment of unresectable NF2-deficient malignant pleural mesothelioma.
IK-930 is a TEAD inhibitor designed to target the Hippo signaling pathway.
Earlier this year, IK-930 was granted the FDA orphan drug designation for the treatment of patients having malignant pleural mesothelioma.
Ikena Oncology gets FDA fast track designation for IK-930 in mesothelioma. Photo courtesy of Bluerasberry/Wikipedia.org.
Sergio Santillana — Chief Medical Officer at Ikena Oncology said: “We are delighted to announce that IK-930 has been granted Fast Track designation, demonstrating the potential of IK-930 to address the unmet medical need of people with unresectable NF2-deficient MPM.
“This milestone, combined with the Orphan Drug designation in mesothelioma, further validates our targeted oncology approach to address significant unmet medical needs for difficult-to-treat cancers and supports our goal to advance the development of IK-930 for the patients who potentially could benefit most.”
Presently, IK-930 is being evaluated as a monotherapy in a phase 1 clinical trial in patients having advanced solid tumors irrespective of gene alterations in the Hippo pathway.