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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Page 1 of 1 (3 locations)

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