A First-in-Human FIH, Phase 1, Multicenter, Open-label, Dose Escalation and Expansion Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of Orally Administered GLB-001 in Patients with Refractory or Relapsed Acute Myeloid Leukemia R/R AML or Refractory or Relapsed Higher-risk Myelodysplastic Syndromes R/R HR-MDS

Brief Summary

Type:
Leukemias

Study Type:
Treatment

Phase:
I

ClinicalTrials.gov Identifier:
NCT06146257

Study #:
STUDY00150562

Start Date:
Nov 30, 2023

Full Details and Eligibility at clinicaltrials.gov

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ClinicalTrials.gov ID: NCT06146257

View Complete Trial Details & Eligibility at ClinicalTrials.gov