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An extention study of JR-401 in patients with SHOX dificiency

Not Applicable
Conditions
SHOX deficiency
Registration Number
JPRN-jRCT2031200425
Lead Sponsor
Ibaraki Ryo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
19
Inclusion Criteria

A pediatric Patient who participated in the previous study and completed the visit after 24 months, and who were judged by the principal-investigator or sub-investigator to be safe for transfer to this study from the viewpoint of safety

Exclusion Criteria

A pediatric patient with a diagnosis of diabetes (following the Diagnostic Procedure for Diabetes)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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