A Study of JR-141 in Patients With Mucopolysaccharidosis II (BR21)

JCR Pharmaceuticals

Status and phase

Completed

Phase 2

Conditions

Mucopolysaccharidosis II

Treatments

Drug: JR-141

Study type

Interventional

Funder types

Industry

Identifiers

NCT03359213

JR-141-BR21

Details and patient eligibility

About

A Phase II open-label, randomized, parallel group, 2 sites (Brazil), designed to evaluate the safety and efficacy of 3 doses of study drug for the treatment of the MPS II.

Enrollment

18 patients

Sex

Male

Volunteers

No Healthy Volunteers

Inclusion criteria

Males with confirmed diagnosis of MPS II, based on deficient activity of IDS in leucocytes or fibroblasts and/or pathogenic mutations identified in the IDS gene (if enzyme diagnosis was in dried blood spots or plasma, molecular genetics confirmation is mandatory).
One of the following age groups:
1. 0 to 3 years and 11 months old (6 patients, 2 in each dose)
2. 4 years to 7 years and 11 months old (6 patients, 2 in each dose)
3. 8 years or older (6 patients, 2 in each dose)
Capable of providing written consent by himself, unless the patient is under the age of 18 years at the time of informed consent process, or it is not possible to obtain consent from the patient himself due to his intellectual disabilities associated with MPS II.
In the case of a patient who is under the age of 18 years or from whom it is not possible to obtain consent due to his intellectual disabilities associated with MSP II, he may be included if written consent can be provided by legal representative; however written consent should be obtained from the patient himself too, wherever possible.
Naïve patients or patients who are receiving enzyme replacement therapy with idursulfase could be included if provided treatment has been stable in the last 6 months and agree to interrupt the treatment at least one week before the first study drug infusion, and agree in suspending this treatment for the duration of the trial.

Exclusion criteria

Refusal to sign the informed consent form.
Unable to perform the study procedures, except for neurocognitive testing.
Previous engrafted BMT/HSCT.
Surgical or other major medical intervention planned to occur before week 26.
Participation in a clinical trial with an investigational drug in the last 12 months.
Judged by the investigator or subinvestigator as being unable to undergo lumbar puncture, including those who have difficulties in taking a position for lumber puncture due to joint contracture or those who are likely to experience difficulty breathing during the lumbar puncture process.
Judged by the investigator or subinvestigator to be ineligible to participate in the study due to a history of a serious drug allergy or sensitivity.
Otherwise judged by the investigator or subinvestigator to be ineligible to participate in the study out of consideration for the subject safety.