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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

Trial Profile

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

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 10 Dec 2024

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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.

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