Study to Evaluate the Efficacy and Safety of Nizubaglustat (AZ-3102) in Patients With Gaucher Dis… (NCT07715084) | Clinical Trial Compass
Not Yet RecruitingPhase 2
Study to Evaluate the Efficacy and Safety of Nizubaglustat (AZ-3102) in Patients With Gaucher Disease Type 3 (GD3)
India, Pakistan, Turkey (Türkiye)20 participantsStarted 2026-09-28
Plain-language summary
A 96-week, open-label, Phase 2 study to evaluate the efficacy and safety of Nizubaglustat (AZ-3102) in patients with Gaucher disease type 3 (GD3).
Who can participate
Age range
4 Years – 30 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Have a confirmed diagnosis of GD3 disease
* Have at least 2 impaired domains in the Modified Severity Scoring Tool (mSST) at Screening
* Be aged 4-30 years old at the time of informed consent
* Have the following symptoms of GD3 identified at Screening: GD-related anemia, thrombocytopenia, splenomegaly
* Female participants of childbearing potential who are sexually active and willing to follow contraceptive guidance
* Male participants with a female partner of childbearing potential who are willing to follow contraceptive guidance
Exclusion Criteria:
* Any condition at Screening or Baseline that, in the opinion of the Principal Investigator, could interfere with study assessments
* History of medical conditions other than GD3 that, in the opinion of the Principal Investigator, could confound scientific rigor or interpretation of results
* Body weight \<10 kg at Screening
* Presence of a neurologic disease other than GD3
* Transfusion dependence
* Prior splenectomy
* The presence of severe renal impairment at Screening
* Prior use of an investigational drug within 3 months before Screening
* Prior participation in a clinical study involving gene therapy or stem cell transplantation
* Current treatment, or treatment in the last 12 months before Screening, with enzyme replacement therapy (ERT) and/or substrate reduction therapy (SRT)
* A positive serum pregnancy test (for women of childbearing potential)
* Electrocardiogram (ECG) with an average Frideri…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.