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Safety study of NaPPS in pediatric patients with mucopolysaccharidosis type VI

Safety study of NaPPS in pediatric patients with mucopolysaccharidosis type VI

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223060
Enrollment
2
Registered
2016-01-04
Start date
2016-01-04
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

mucopolysaccharidosis type VI

Interventions

investigational material(s) Generic name etc : NaPPS INN of investigational material : Therapeutic category code : 399 Agents affecting metabolism, n.e.c. Dosage and Administration for Investigationa

Sponsors

ReqMed Company, Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients who are confirmly diagnosed with Mucopolysaccharidosis type VI and have assessable symptoms of cartilage and bone. (2) Patients who are able to explain their own condition or to show their own intention. (3) Patients who are able to walk for 6 minutes continuously.

Exclusion criteria

Exclusion criteria:

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026