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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take GLB-001

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

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