NCT07082543

Brief Summary

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 GM1 gangliosidosis or GM2 gangliosidosis

Trial Health

88
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
75

participants targeted

Target at below P25 for phase_3

Timeline
19mo left

Started Jun 2025

Geographic Reach
16 countries

36 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress36%
Jun 2025Nov 2027

First Submitted

Initial submission to the registry

June 27, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

June 30, 2025

Completed
24 days until next milestone

First Posted

Study publicly available on registry

July 24, 2025

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 4, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 4, 2027

Last Updated

May 5, 2026

Status Verified

September 1, 2025

Enrollment Period

2.3 years

First QC Date

June 27, 2025

Last Update Submit

April 30, 2026

Conditions

Keywords

Nizubaglustat

Outcome Measures

Primary Outcomes (2)

  • Change from baseline in total Scale for the Assessment and Rating of Ataxia (SARA) score

    Total SARA comprises eight categories with a cumulative score ranging from 0 (no ataxia) to 40 (most severe ataxia)

    Baseline to month 18

  • Change from baseline in functional SARA score

    Functional SARA uses an abbreviated scale that scores 0 to 16, with higher scores indicating more severe impairment

    Baseline to month 18

Secondary Outcomes (20)

  • Change from baseline in SARA score for gait/posture

    Baseline to months 6, 12, and 18

  • Change from baseline in SARA score for speech

    Baseline to months 6, 12, and 18

  • Change from baseline in SARA score for kinetics

    Baseline to months 6, 12, and 18

  • Change from baseline in Vineland Adaptive Behavior Scale (VABS)

    Baseline to months 6, 12, and 18

  • Change from baseline in Penetration-Aspiration Scale (PAS)

    Baseline to months 6, 12, and 18

  • +15 more secondary outcomes

Study Arms (2)

Nizubaglustat

EXPERIMENTAL

Once daily oral dispersible tablets

Drug: AZ-3102

Placebo

PLACEBO COMPARATOR
Drug: Placebo

Interventions

Placebo

Placebo

Nizubaglustat

Nizubaglustat

Eligibility Criteria

Age4 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Confirmed GM1 gangliosidosis or Tay-Sachs, Sandhoff, or GM2AB variant
  • Male and female participants aged 4 years and older at the time of informed consent
  • Onset of neurological symptoms from 1 to 10 years
  • Disability level at Baseline: Ataxic disturbances with a total SARA score of ≥3 and ≤30 at Baseline
  • Females of childbearing potential who are sexually active willing to follow the contraceptive guidance
  • Male participants with a female partner of childbearing potential willing to follow the contraceptive guidance

You may not qualify if:

  • A history of medical conditions other than GM1 or GM2 gangliosidosis that, in the opinion of the Principal Investigator, would confound scientific rigor or the interpretation of results
  • Body weight of \<10 kg
  • The presence of another neurologic disease
  • The presence of moderate or severe hepatic impairment
  • The presence of moderate or severe renal impairment
  • Platelet count of \<100x10\^9/L
  • The dose of any anti-epileptic treatment(s) was not stable (required a change in dose within the previous 3 months) and/or a new anti-epileptic treatment (drug or procedure) was prescribed in the month before Baseline
  • Prior use of an investigational drug within the 3 months before Screening; or prior participation in a clinical study involving gene therapy or stem cell transplantation within 2 years prior to Screening
  • A positive serum pregnancy test (for women of childbearing potential)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (36)

UCSF Children's Hospital and Research Center at Oakland

Oakland, California, 94609, United States

RECRUITING

University of Minnesota Medical School

Minneapolis, Minnesota, 55455, United States

NOT YET RECRUITING

Mayo Clinic Children's Center - PIN

Rochester, Minnesota, 55905, United States

RECRUITING

Children's Medical Center Dallas

Dallas, Texas, 75235, United States

NOT YET RECRUITING

Lysosomal Rare Disorders Research and Treatment Center

Fairfax, Virginia, 22030-7404, United States

RECRUITING

Hospital Universitario Austral

Ciudad Autónoma Buenos Aires, Buenos Aires, B1629AHJ, Argentina

RECRUITING

Hospital de Niños de La Santisima Trinidad

Córdoba, Córdoba Province, X5004 ASL, Argentina

RECRUITING

Women's and Children's Hospital

North Adelaide, South Australia, 5006, Australia

RECRUITING

Royal Children's Hospital Melbourne - PIN

Parkville, Victoria, 3052, Australia

NOT YET RECRUITING

Instituto Fernandes Figueira

Rio de Janeiro, Rio de Janeiro, 22250-020, Brazil

NOT YET RECRUITING

Hospital de Clinicas de Porto Alegre (HCPA) - PPDS

Porto Alegre, Rio Grande do Sul, 90560-030, Brazil

RECRUITING

Hospital Pequeno Principe

Curitiba, Brazil

NOT YET RECRUITING

M.A.G.I.C. Clinic Ltd. Metabolics and Genetics in Calgary

Calgary, Alberta, T3B 6A8, Canada

NOT YET RECRUITING

University of Alberta Medical Genetics Clinic

Edmonton, Alberta, T6G 2B7, Canada

NOT YET RECRUITING

Centre Hospitalier de l'Universite de Montreal-1000 rue Saint-Denis

Montreal, Quebec, H2X 0C1, Canada

NOT YET RECRUITING

AP-HP - Hôpital Armand Trousseau

Paris, 75012, France

RECRUITING

SphinCS GmbH

Höchheim, 65239, Germany

NOT YET RECRUITING

Amrita Institute of Medical Sciences and Research Centre

Ernākulam, Kerala, 682041, India

RECRUITING

All India Institute of Medical Sciences (AIIMS) - New Delhi

New Delhi, National Capital Territory of Delhi, 110029, India

RECRUITING

JK Lone Hospital

Jaipur, Rajasthan, 302004, India

RECRUITING

Christian Medical College and Hospital

Vellore, Tamil Nadu, 632004, India

NOT YET RECRUITING

Fondazione IRCCS Istituto Neurologico Carlo Besta

Milan, 20133, Italy

RECRUITING

Hospital Universitario Dr. Jose Eleuterio González

Monterrey, Nuevo León, 64460, Mexico

NOT YET RECRUITING

Centenario Hospital Miguel Hidalgo

Aguascalientes, 20000, Mexico

NOT YET RECRUITING

ULS de Santo António, EPE - Centro Materno Infantil Norte

Porto, Porto District, 4050-651, Portugal

RECRUITING

ULS de Santa Maria,EPE - Hospital de Santa Maria - PPDS

Lisbon, 1649-035, Portugal

RECRUITING

Hospital Universitario Vall d'Hebron - PPDS

Barcelona, Barcelona, 8035, Spain

RECRUITING

Hospital Infantil Universitario Niño Jesus - PIN

Madrid, Madrid, 28009, Spain

RECRUITING

Sahlgrenska universitetssjukhuset Östra

Gothenburg, Västra Götaland County, 416 50, Sweden

RECRUITING

Inselspital - Universitätsspital Bern

Bern, Canton of Bern, 3010, Switzerland

RECRUITING

Balcali Hastanesi Saglik Uygulama ve Arastirma Merkezi

Adana, Adana, 1250, Turkey (Türkiye)

NOT YET RECRUITING

Gazi Universitesi Saglik Arastirma ve Uygulama Merkezi

Çankaya, Ankara, 6500, Turkey (Türkiye)

RECRUITING

Ege Universitesi Tip Fakultesi

Bornova, İzmir, 35100, Turkey (Türkiye)

NOT YET RECRUITING

University College London Hospitals (UCLH)

London, Middlesex, WC1N 3BG, United Kingdom

NOT YET RECRUITING

Great Ormond Street Hospital NHSFT

London, United Kingdom

NOT YET RECRUITING

Royal Manchester Children's Hospital

Manchester, M13 9WL, United Kingdom

NOT YET RECRUITING

MeSH Terms

Conditions

Gangliosidoses, GM2Gangliosidosis, GM1

Condition Hierarchy (Ancestors)

GangliosidosesSphingolipidosesLysosomal Storage Diseases, Nervous SystemBrain Diseases, Metabolic, InbornBrain Diseases, MetabolicBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesMetabolism, Inborn ErrorsGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesLipidosesLipid Metabolism, Inborn ErrorsLysosomal Storage DiseasesMetabolic DiseasesNutritional and Metabolic DiseasesLipid Metabolism Disorders

Central Study Contacts

Patient Advocacy Representative

CONTACT

Contact for Healthcare Professionals

CONTACT

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 27, 2025

First Posted

July 24, 2025

Study Start

June 30, 2025

Primary Completion (Estimated)

November 4, 2027

Study Completion (Estimated)

November 4, 2027

Last Updated

May 5, 2026

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations