Early Access Program With Arimoclomol in US Patients With NPC

NCT04316637 | Unknown

• 1 other identifier: OR-ARI-EAP-NPC
• Study Type: expanded_access
• Target: N/A
• Locations: 1 country
• Sites: 13

Brief Summary

NPC is a rare, relentlessly progressive, neurological disease and associated with serious morbidity and shortened life expectancy. The purpose of this Expanded Access Program is to provide early access to arimoclomol for patients with Niemann-Pick Type C disease who, in the opinion and the clinical judgement of the treating physician, may benefit from treatment with arimoclomol. Participants will receive treatment with arimoclomol until their doctor finds it does not help them anymore, they withdraw, or the study is stopped for any reason.

Conditions

Niemann-Pick Disease, Type C

Interventions

Arimoclomol DRUG

Participants receive prescribed arimoclomol by oral administration

Eligibility Criteria

• Age: 2 Years+
• Sex: all
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• The patient has a confirmed diagnosis of NPC (NPC1 or NPC2)\* and at least one neurological symptom.
• The patient is two years of age or above.
• The patient is a permanent resident of US.
• If taking miglustat (Zavesca®), the patient must have been on the target dose for the past six weeks.
• If the patient is a sexually active female of child-bearing potential (post-menarche), it is agreed to use highly effective contraception during the EAP and until three weeks after the last dose of arimoclomol.
• Confirmed negative urine pregnancy test for sexually active female of child-bearing potential (post-menarche).
• All sexually active male patients with female partners of child-bearing potential (postmenarche) agree to use a condom in addition to the birth control used by their partners during treatment and until three weeks after the last dose of arimoclomol.
• If the patient has a history of seizures, the condition must be adequately controlled, i.e., the pattern of seizure activity must be stable, and the patient must be on a stable dose and regimen of antiepileptic medication during one month prior to screening.
• Patient or parent/guardian must provide written informed consent to participate in EAP.
• In line with Patterson et al. 2017

You may not qualify if:

• Severe liver insufficiency.
• Renal insufficiency.
• The patient has a known or suspected allergy or intolerance to arimoclomol or its constituents.
• The patient is pregnant, planning to become pregnant (while on the EAP program) or is currently breastfeeding.
• The patient will undergo treatment with another investigational drug\*, whilst participating in the program or in the 4 weeks prior to commencing treatment with arimoclomol.
• The patient is either eligible and able to participate in or is currently participating in an active interventional clinical trial within the indication.
• The patient, in the opinion of the clinician, is unable to comply with the treatment or has a medical condition that would potentially increase the risk to the patient by participation.
• The patient has a medical condition which hinders the clinician's assessment of arimoclomol safety and efficacy (e.g. certain epileptic conditions or severe cataplexy).
• Including unlicensed product provided under an Early Access Program or equivalent compassionate use programs

Sponsors & Collaborators

• ZevraDenmark: lead

Study Sites (13)

University of Alabama Birmingham

Birmingham, Alabama, 35233, United States

AVAILABLE

UCSF Benioff Children's Hospital and Research Center/ UCSF

Oakland, California, 94609, United States

AVAILABLE

Children's Hospital of Orange County (CHOC)

Orange, California, 92868, United States

AVAILABLE

Nicklaus Children's Hospital

Miami, Florida, 33155, United States

AVAILABLE

Rush University Medical Center

Chicago, Illinois, 60612, United States

AVAILABLE

Boston Childrens Hospital

Boston, Massachusetts, 02215, United States

AVAILABLE

Mayo Clinic Children's Center

Rochester, Minnesota, 55905, United States

AVAILABLE

New York University School of Medicine

New York, New York, 10017, United States

AVAILABLE

Cincinnati Children's Hospital Medical Center (CCH)

Cincinnati, Ohio, 45229, United States

AVAILABLE

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, 19104, United States

AVAILABLE

UPMC Children's Hospital of Pittsburgh

Pittsburgh, Pennsylvania, 15224, United States

AVAILABLE

Dell Children's Medical Center

Austin, Texas, 78723, United States

AVAILABLE

UT Health / McGovern Medical School; Division of Medical Genetics

Houston, Texas, 77030, United States

AVAILABLE

MeSH Terms

Conditions

Niemann-Pick Disease, Type C

Interventions

arimoclomol

Condition Hierarchy (Ancestors)

Niemann-Pick Diseases; Sphingolipidoses; Lysosomal Storage Diseases, Nervous System; Brain Diseases, Metabolic, Inborn; Brain Diseases, Metabolic; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Histiocytosis, Non-Langerhans-Cell; Histiocytosis; Lymphatic Diseases; Hemic and Lymphatic Diseases; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Lipidoses; Lipid Metabolism, Inborn Errors; Lysosomal Storage Diseases; Metabolic Diseases; Nutritional and Metabolic Diseases; Lipid Metabolism Disorders

Central Study Contacts

Zevra Therapeutics Medical Information

CONTACT

+1-888-289-5607; medicalaffairs@zevra.com

Clinigen Customer service

CONTACT

+1 877-768-4303; usmapoperations@clinigengroup.com

Study Design

• Study Type: expanded access
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 18, 2020
• First Posted: March 20, 2020
• Last Updated: August 16, 2024

Record last verified: 2024-08

Locations

US (13)