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Extension Study of AGT-181-102 to Evaluate Long Term Safety and Activity of AGT-181

Phase 1
Completed
Conditions
Mucopolysaccharidosis I
Interventions
Registration Number
NCT02597114
Lead Sponsor
ArmaGen, Inc
Brief Summary

AGT-181 is a fusion protein containing alpha-L-Iduronidase that is intended to deliver the enzyme peripherally and to the brain, when administered intravenously. This study is an extension of a safety and dose ranging study to obtain long term safety and exposure data, as well as information on the biological activity of the investigational drug

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3
Inclusion Criteria
  • Must have completed clinical trial AGT-181-102
  • Voluntary written consent by patient or legally responsible representative
  • All women of childbearing potential and sexually mature males must be advised to use a medically accepted method of contraception throughout the study.
  • Negative pregnancy test (females)
Exclusion Criteria
  • Refusal to complete screening evaluations.
  • Any medical condition or other circumstances that may significantly interfere with study compliance
  • Patient is pregnant or lactating
  • Clinically significant spinal cord compression, evidence of cervical instability.
  • Subject developed clinically relevant hypersensitivity to AGT-181

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
AGT-181AGT-181AGT-181 (fusion protein of anti-human insulin receptor monoclonal antibody and alpha-L-iduronidase) administered once weekly x 26 weeks at same dose level as subject received in core study
Primary Outcome Measures
NameTimeMethod
Number of participants with adverse events as a measure of safety and tolerability104 weeks (2 years)
Secondary Outcome Measures
NameTimeMethod
changes in urinary or plasma glycosaminoglycans (GAGs)104 weeks (2 years)
change in spleen size104 weeks (2 years)
change in levels of heparan sulfate and dermatan sulfate in the cerebrospinal fluid104 weeks (2 years)
change in liver size104 weeks (2 years)
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