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 (NPC)
a study on Niemann-Pick Disease GM1 Gangliosidosis
Summary
- Eligibility
 - for people ages 4 years and up (full criteria)
 - Location
 - at UCSF
 - Dates
 - study startedstudy ends around
 
Description
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 Niemann-Pick type C disease
Official Title
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
Details
Please see NCT #07054515 for information on the AZA-001-301 Master Protocol
PRIMARY OBJECTIVE
The primary objective of this study is to demonstrate superior efficacy on ataxic manifestations with oral nizubaglustat dosing compared with placebo when administered over 18 months in participants with late-infantile and juvenile forms of NPC disease
SECONDARY OBJECTIVES
- To assess additional efficacy in ataxic and non-ataxic manifestations comparing nizubaglustat dosing with placebo when administered over 18 months in participants with late-infantile and juvenile forms of NPC disease
 
II. To assess the pharmacokinetic (PK) properties of nizubaglustat after administration of the first dose (Visit 1) and at steady state after multiple once daily doses
III. To assess the pharmacodynamic (PD) effects of nizubaglustat
IV. To assess the safety and tolerability of daily oral nizubaglustat dosing compared with placebo, when administered over 18 months in participants with late-infantile and juvenile forms of NPC disease
Keywords
Niemann-Pick Type C Disease, Nizubaglustat, Type C Niemann-Pick Disease
Eligibility
You can join if…
Open to people ages 4 years and up
- Signed informed consent
 - Confirmed diagnosis of NPC disease
 - Patient is unable or unwilling to take miglustat, or is, in the opinion of the investigator, unsatisfactorily treated with miglustat
 - Male and female participants aged 4 years and older at the time of informed consent
 - Onset of neurological symptoms from 2 to 15 years
 - Disability level at Baseline: Ataxic disturbances with a total SARA score of ≥3 and ≤30 at Baseline
 - Female 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 CAN'T join if...
- A history of medical conditions other than NPC disease 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 <100x109/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)
 - Current treatment with miglustat, provided the patient has been using the recommended dose for most of the past 12 months AND is, in the opinion of the investigator, satisfactorily treated with miglustat. Any participants receiving miglustat are required to undergo a 1-month washout period before starting study medication
 
Locations
- Children's Hospital and Research Center at Oakland
not yet accepting patients 
Oakland 5378538 California 5332921 94609 United States - M.A.G.I.C. Clinic Ltd. Metabolics and Genetics in Calgary
not yet accepting patients 
Calgary 5913490 Alberta 5883102 T3B 6A8 Canada - ULS de Santo António, EPE - Centro Materno Infantil Norte
accepting new patients 
Porto 2735943 Porto District 2735941 4050-651 Portugal - Hospital Universitario Vall d'Hebron - PPDS
accepting new patients 
Barcelona 3128760 Barcelona 8035 Spain - Hospital Infantil Universitario Niño Jesus - PIN
accepting new patients 
Madrid 3117735 Madrid 3117732 28009 Spain 
Details
- Status
 -  accepting new patients at some sites,
but this study is not currently recruiting here - Start Date
 - Completion Date
 - (estimated)
 - Sponsor
 - Azafaros A.G.
 - ID
 - NCT07082725
 - Phase
 - Phase 3 research study
 - Study Type
 - Interventional
 - Participants
 - Expecting 72 study participants
 - Last Updated