Phase I/II Study of JR-441 in Patients With Mucopolysaccharidosis Type IIIA

JCR Pharmaceuticals

Status and phase

Enrolling

Phase 2

Phase 1

Conditions

Mucopolysaccharidosis III-A

Treatments

Drug: JR-441

Study type

Interventional

Funder types

Industry

Identifiers

NCT06095388

JR-441-101

2022-002314-17 (EudraCT Number)

Details and patient eligibility

About

A Phase I/ II, open-label, randomized, 2-arm study, designed to evaluate the safety and explore efficacy of the study drug in development for the treatment of MPS IIIA patients.

Enrollment

12 estimated patients

Sex

All

Ages

1 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Chronological age of ≥1 year and ≤18 years.
Confirmed diagnosis of MPS IIIA.
Body weight ≥ 10 kg.

Exclusion criteria

Prior experience to gene therapy or HSCT with successful engraftment.
Past use of another investigational drug or product in last 4 months or 5 half-lives (whichever is longer) before signing ICF.
Current participation in a clinical trial or past participation (within 30 days of enrolment into this study) in a study involving invasive procedures.
Past use of Genistein or Kineret (anakinra) within 4 months before signing ICF.
Serious drug allergy or hypersensitivity.
Contraindication for lumbar puncture or MRI.
History of bleeding disorder or current use of medications that, in the opinion of the investigator, place them at risk of bleeding following lumbar puncture.

The above information is not intended to contain all considerations relevant to a patient's potential participation in this clinical trial.