Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

GLB-001 clinical trials

Also listed in trial records as GLB-C183-A-2
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our USA, China and Japan registers that name GLB-001 as an intervention. Synced 11 Nov 2026
2Current trials
2Recruiting now
2Lead sponsors
3Country registers
At a glance

GLB-001 is named as an intervention in 2 current clinical trials in our USA, China and Japan registers. 2 are recruiting patients now. All registered phases are Phase 1. The sponsor with the most trials is GluBio Therapeutics Inc (1). The most-studied condition is Myelodysplastic Syndromes.

Patient leaflets for GLB-001

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting2100%

Trials by phase

  • Phase 12100%
01

Clinical trials of GLB-001

2 trials
StudyPhaseStatusLead sponsorRegisters
A Study of GLB-001 in Patients With Relapsed or Refractory Acute Myeloid Leukemia or Relapsed or Refractory Higher Risk Myelodysplastic Syndromes
NCT06146257 · Acute Myeloid Leukemia, Myelodysplastic Syndromes
Phase 1 Recruiting GluBio Therapeutics Inc USA
A Study of GLB-001 in Patients With Myeloid Malignancies
NCT06378437 · ClinicalTrials.gov ↗ · Polycythemia Vera, Essential Thrombocythemia, Myelofibrosis
Phase 1 Recruiting Hangzhou GluBio Pharmaceutical Co., Ltd China, Japan

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with GLB-001

5 conditions
Myelodysplastic Syndromes2Acute Myeloid Leukemia1Polycythemia Vera1Essential Thrombocythemia1Myelofibrosis1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
GluBio Therapeutics Inc1
Hangzhou GluBio Pharmaceutical Co., Ltd1
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA11
Clinical trials in China11
Clinical trials in Japan11

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about GLB-001 trials

How many clinical trials are testing GLB-001?

2 current trials in our USA, China and Japan registers name GLB-001 (also registered as GLB-C183-A-2) as a drug or biological intervention, as of the registry sync on 11 November 2026. Completed and withdrawn studies are not counted.

Are GLB-001 trials recruiting patients?

Yes. 2 of the 2 trials are recruiting: 1 with sites in USA, 1 with sites in China and 1 with sites in Japan. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors GLB-001 clinical trials?

GluBio Therapeutics Inc (1) and Hangzhou GluBio Pharmaceutical Co., Ltd (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how GLB-001 works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how GLB-001 works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists GLB-001 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 11 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.