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Study details
Enrolling now

A Study of GLB-001

GluBio Therapeutics Inc.
NCT IDNCT06146257ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

48

Study length

about 2.7 years

Ages

18+

Locations

8 sites in CA, KS, NY +1

About this study

This trial is testing a new treatment called GLB-001 in people with leukemia or myelodysplastic syndromes that have returned after treatment. The goal is to see if this medication is safe and how it works in the body.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take GLB-001
PhasePhase 1
Primary goalDose-limiting Toxicity (DLT)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Dose-limiting Toxicity (DLT), Incidence of Adverse Events (AEs), Maximum Tolerated Dose (MTD)/Maximum Administered Dose (MAD), Recommended Phase 2 Dose (RP2D)

Secondary: CR Rate in Participants with Higher Risk Myelodysplastic Syndromes (HR-MDS), CR with Incomplete Hematologic Recovery (CRi) Rate in Participants with AML, CR with Partial Hematological Recovery (CRh) Rate in Participants with AML, Complete Remission (CR) Rate in Participants with AML, DOR in Participants with HR-MDS, Duration of Remission or Response (DOR) in Participants with AML, GLB-001 Pharmacokinetics-AUC0-24, GLB-001 Pharmacokinetics-AUC0-last

Body systems

Oncology