A Phase 1, First-in-Human Study of IK-930, an Oral TEAD Inhibitor Targeting the Hippo Pathway in Subjects With Advanced Solid Tumors
Latest Information Update: 19 Jun 2024
At a glance
- Drugs IK 930 (Primary)
- Indications Haemangioendothelioma; Mesothelioma; Soft tissue sarcoma; Solid tumours
- Focus Adverse reactions; First in man; Proof of concept
- Sponsors Ikena Oncology
- 13 Jun 2024 Status changed from discontinued to active, no longer recruiting.
- 28 May 2024 According to an Ikena Oncology media release, based on a review of clinical data to date, available resources, and the Company's strategic priorities, the Company decided to discontinue development of IK-930. The IK-930 Phase 1 program will begin winddown activities; treatment will continue for patients enrolled to date who have derived benefit. The Company will seek strategic options for the program, including potential partners for development of IK-930 in combination with other targeted agent
- 28 May 2024 Status changed from recruiting to discontinued, according to an Ikena Oncology media release.