A Phase I, First-In-Human, Multicenter, Open Label, Dose Escalation and Dose Expansion Study to Evaluate the Safety and Efficacy of ABM-168 Administered Orally in Adult Patients with Advanced Solid Tumors
Latest Information Update: 10 Dec 2024
At a glance
- Drugs ABM 168 (Primary)
- Indications Brain cancer; Brain metastases; Solid tumours
- Focus Adverse reactions; First in man
- Sponsors ABM Therapeutics
Most Recent Events
- 06 Dec 2024 Status changed from recruiting to discontinued. (Reason the study was stopped: Due to development strategy change).
- 04 May 2023 According to an ABM Therapeutics media release, company announced first patient was successfully dosed.
- 14 Apr 2023 Status changed from planning to recruiting.