An Open-label Phase I/II Study of JR-446 in Mucopolysaccharidosis Type IIIB

Last updated: February 3, 2025
Sponsor: JCR Pharmaceuticals Co., Ltd.
Overall Status: Active - Recruiting

Phase

1/2

Condition

N/A

Treatment

JR-446

Clinical Study ID

NCT06488924
JR-446-101
  • Ages < 17
  • All Genders

Study Summary

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

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Chronological age of <18 years

  • Confirmed diagnosis of MPS IIIB

Exclusion

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 ofenrolment 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 ofthe 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.

Study Design

Total Participants: 10
Treatment Group(s): 1
Primary Treatment: JR-446
Phase: 1/2
Study Start date:
November 05, 2024
Estimated Completion Date:
December 05, 2028

Connect with a study center

  • Hiroshima University Hospital

    Hiroshima,
    Japan

    Site Not Available

  • University of the Ryukyus Hospital

    Okinawa,
    Japan

    Active - Recruiting

  • National Center for Child Health and Development

    Tokyo,
    Japan

    Site Not Available

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