A Study to Evaluate the Safety and Efficacy of Oral Nizubaglustat (AZ-3102) in Late-infantile and Juvenile Forms of Niemann-Pick Type C Disease, GM1 Gangliosidosis or GM2 Gangliosidosis

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age4+
SponsorAzafaros B.V.

About this trial

An 18-month double-blind, randomized, placebo-controlled, multicenter, Phase 3 study to evaluate the safety and efficacy of oral nizubaglustat (AZ-3102) in late-infantile and juvenile forms of Niemann-Pick type C disease and in late-infantile and juvenile-onset forms of GM1 gangliosidosis or GM2 gangliosidosis

Eligibility criteria

Qualifiers

Male and female participants, aged 4 years and older with a diagnosis of the late-infantile or juvenile form of NPC disease. Detailed inclusion criteria are presented in the NPC disease-specific subprotocol AZA-001-301-NPC (NCT07082725).

Male and female participants, aged 4 years and older with a diagnosis of GM1 or GM2 (Tay-Sachs, Sandhoff, or GM2AB variant disease) gangliosidosis of late-infantile/ juvenile onset. Detailed inclusion criteria are presented in the GM1/GM2 gangliosidosis-specific subprotocol AZA-001-301-GMx (NCT07082543).

Disqualifiers

Detailed exclusion criteria are presented in the NPC disease-specific subprotocol AZA-001-301-NPC

Detailed exclusion criteria are presented in the GM1/GM2 gangliosidosis-specific subprotocol AZA-001-301-GMx

Trial design

Treatments tested in this trial

  • AZ-3102
  • Placebo

Treatment groups

147 Participants
are divided into 2 treatment groups

Locations

38
Argentina
Hospital Universitario AustralB1629AHJ, Ciudad Autónoma Buenos AiresBuenos Aires, Argentina
Hospital de Niños de La Santisima TrinidadX5004 ASL, CórdobaCórdoba Province, Argentina
Australia
Women's and Children's Hospital5006, North AdelaideSouth Australia, Australia
Royal Children's Hospital Melbourne - PIN3052, ParkvilleVictoria, Australia

Sponsors and collaborators

Azafaros B.V.

Lead sponsor