Gaucher Disease Type 3: Clinical Trials

4 trials for Gaucher Disease Type 3, newest first

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3 not yet recruiting, 1 active not recruiting. 4 Phase 2, 1 Phase 1, 1 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 24Not yet recruiting 3, Active not recruiting 1
Phase 11Not yet recruiting 1
Phase 31Not yet recruiting 1

Follow Gaucher Disease Type 3: new trials by email Literature Review of Gaucher Disease Type 3 trials Research Report on Gaucher Disease Type 3

Trials (filtered) newest first · largest first

All 4 trials

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Study to Evaluate the Efficacy and Safety of Nizubaglustat (AZ-3102) in Patients With Gaucher Disease Type 3 (GD3)
AZ-3102 - Gaucher Disease Type 3
Phase 2Not yet recruitingAzafaros B.V.202027-01-252026-11-12
Long-Term Safety and Tolerability of Nizubaglustat in Participants With Rare Lysosomal Disorders
AZ-3102 - Niemann-Pick Disease Type C, GM2 Gangliosidosis
Phase 2 / Phase 3Not yet recruitingAzafaros B.V.2182026-12-102026-10-21
A Phase I/II Clinical Study to Evaluate the Safety and Efficacy of VGN-R08b in Patients With Type III Gaucher's Disease
VGN-R08b - Gaucher Disease Type 3
Phase 1 / Phase 2Not yet recruitingShanghai Vitalgen BioPharma Co., Ltd.122026-05-142026-05-22
Venglustat in Combination With Cerezyme in Adult Patients With Gaucher Disease Type 3 With Venglustat Monotherapy Extension
venglustat (GZ402671), imiglucerase - Gaucher Disease Type 1, Gaucher Disease Type 3
Phase 2Active not recruitingGenzyme, a Sanofi Company122017-01-042026-07-10

Narrower conditions

Gaucher Disease (4)  ·  Gangliosidoses, GM2 (1)  ·  Gangliosidosis, GM1 (1)  ·  Niemann-Pick Disease, Type C (1)

Broader conditions

Brain Diseases (4)  ·  Brain Diseases, Metabolic (4)  ·  Brain Diseases, Metabolic, Inborn (4)  ·  Central Nervous System Diseases (4)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (4)  ·  Genetic Diseases, Inborn (4)  ·  Lipid Metabolism Disorders (4)  ·  Lipid Metabolism, Inborn Errors (4)  ·  Lipidoses (4)  ·  Lysosomal Storage Diseases (4)  ·  Lysosomal Storage Diseases, Nervous System (4)  ·  Metabolic Diseases (4)  ·  Metabolism, Inborn Errors (4)  ·  Nervous System Diseases (4)  ·  Nutritional and Metabolic Diseases (4)

Interventions

imiglucerase (1)  ·  venglustat (1)

Sponsors

Azafaros B.V. (2)  ·  Genzyme, a Sanofi Company (1)  ·  Shanghai Vitalgen BioPharma Co., Ltd. (1)

Countries

Germany (1)  ·  India (1)  ·  Japan (1)  ·  Pakistan (1)  ·  Turkey (Türkiye) (1)  ·  United Kingdom (1)  ·  United States (1)

Results publications

PMID 38802634

NIH funding

2014 (1), 2023 (1)