Natural History Study Protocol in PMM2-CDG (CDG-Ia)

NCT03173300 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2025-11-18

No results posted yet for this study

Summary

Clinical and Basic Investigations into Phosphomannomutase deficiency (PMM2-CDG)

This is a natural history (observational) protocol designed to collect clinical and biological information in patients with PMM2-CDG (CDG-Ia).

Conditions

  • Phosphomannomutase 2 Deficiency

Sponsors & Collaborators

  • Glycomine, Inc.

    lead INDUSTRY

Principal Investigators

  • Chief Medical Officer · Glycomine, Inc.

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-08
Primary Completion
2026-03-31
Completion
2026-03-31

Countries

  • United States
  • Belgium
  • Czechia
  • France
  • Italy
  • Netherlands
  • Poland
  • Portugal
  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03173300 on ClinicalTrials.gov