Status:
RECRUITING
A Study to Evaluate the Safety and Efficacy of Nizubaglustat (AZ-3102) in Patients With GM2 Gangliosidosis or Niemann-Pick Type C Disease
Lead Sponsor:
Azafaros A.G.
Conditions:
GM2 Gangliosidosis
Niemann-Pick Type C Disease
Eligibility:
All Genders
12+ years
Phase:
PHASE2
Brief Summary
This open-label study aims to gather long-term safety, tolerability, PK, biomarker, and clinical efficacy data relating to daily administration of Nizubaglustat in participants previously enrolled in ...
Detailed Description
This is a multicenter, open-label study to assess the safety, tolerability, PK, PD, and efficacy of Nizubaglustat in male or female patients with late-infantile or juvenile onset GM2 gangliosidosis or...
Eligibility Criteria
Inclusion Criteria:
-
Cohort 1 (NPC and GM2 patients):
- Have been randomized into Phase 2 Study AZA-001-5A2-01.
OR
Cohort 2 (NPC patients):
- Be male or female aged ≥12 years
- Have a genetically-confirmed diagnosis of NPC disease
- Have received full-dose Miglustat treatment for at least 12 months and experienced disease stabilization or worsening with treatment over the 2 previous clinic visits. Patients experiencing clinical improvement with Miglustat over the preceding 3 months should not be considered for this study.
- Wish to change treatment to Nizubaglustat for their NPC disease.
- Participants from Phase 2 Study AZA-001-5A2-01 (RAINBOW) who transitioned to Miglustat may be eligible for Cohort 2 if they meet all other criteria.
Participation is supported and deemed beneficial by the Principal Investigator. Be willing and able to be evaluated for all protocol assessments. The participant, parent, and/or legal guardian can read, understand, and sign the informed consent form. Where appropriate, assent will also be sought for participants who have not reached the age of majority.
Exclusion Criteria:
- A positive serum pregnancy test (only tested for women of childbearing potential).
- Female planning to breastfeed during the study.
- Any medical event/condition that prevents participation in the study based on the judgment of the Principal Investigator.
- Participation in another interventional or non-interventional study or early access program.
Key Trial Info
Start Date :
February 4 2026
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 7 2030
Estimated Enrollment :
21 Patients enrolled
Trial Details
Trial ID
NCT07399704
Start Date
February 4 2026
End Date
August 7 2030
Last Update
March 19 2026
Active Locations (3)
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1
Associação Hospitalar de Prot à Infância Dr. Raul Carneiro
Água Verde, Curitiba, Brazil, 80250-060
2
Hospital de Clinicas de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil, 90035-903
3
Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira
Rio de Janeiro, Brazil, 22250